JP2013176366A - Vegfr1-originated peptide and vaccine containing the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an epitope peptide originated from VEGFR1 inducing CTL, capable of becoming a peptide vaccine against diseases mediated by neovascularization, such as tumor.SOLUTION: An epitope peptide comprises a specific amino acid sequence and originated from VEGFR1 having a CTL-inducing ability. An antigen-presenting cell presenting the peptide, and CTL targeting the peptide, and a method for inducing the antigen-presenting cell or CTL. Furthermore, a method for treating and/or preventing a disease mediated by neovascularization, such as tumor, and/or for preventing recurrence thereof after operation, with the peptide, a polynucleotide encoding the peptide, or an antigen-presenting cell presenting the peptide, or a pharmaceutical composition containing CTL targeting the peptide, a method for inducing the CTL, and a method for inducing anti-neovascularization immunization and/or anti-tumor immunization are provided.

Description

  The present invention relates to peptides that are effective in inhibiting angiogenesis and treating and preventing diseases mediated by angiogenesis. The present invention also relates to angiogenesis inhibitors comprising these peptides and pharmaceutical compositions and vaccines for the treatment and / or prevention of diseases mediated by angiogenesis.

Tumor growth is generally limited to 1-2 mm ³ in the absence of a blood supply in which blood vessels are born, and angiogenesis has a critical role in tumor invasion, growth, and metastasis (non-patented Reference 1-4). It has also been shown that inhibition of tumor angiogenesis is associated with suppression of tumor progression. To achieve angiogenesis inhibition, a number of researchers are investigating therapeutic strategies targeting vascular endothelial growth factor (VEGF) and VEGF receptor (VEGFR) that play a critical role in regulating the process of angiogenesis I have done it. These studies have shown that tumor growth can be successfully suppressed in vitro or in vivo using monoclonal antibodies, recombinant receptors, or inhibitors of signaling (Non-Patent Documents 5-10). . However, these strategies require frequent or continuous administration of reagents at relatively high dose levels, which can be associated with considerable inconvenience and adverse effects.

VEGF binds to two related tyrosine kinase receptors, VEGFR1 (Flt-1) and VEGFR2 (KDR), which are strongly expressed on endothelial cells in tumor tissues but not in normal tissues (non-patented) Reference 11-14). VEGFR1 is the first identified VEGF receptor (15), VEGF (VEGF-A), and two other members of the VEGF family, VEGF-B (16) and placenta It interacts with growth factor (PlGF) (Non-patent Document 17). PlGF is expected to move VEGF from VEGFR1 so that more VEGF can bind to VEGFR2 and activate VEGFR2, thereby enhancing angiogenesis driven by VEGF (non-patent literature). 18). Other studies have shown that there is a synergy between VEGF and PlGF in vivo, especially in pathological situations, as evidenced by impaired tumorigenesis and vascular leakage in PlGF-/-mice. (Non-patent Document 19).

  These two receptors for VEGF are also expressed in human choroidal neovascularization (CNV) membranes. However, the role of the VEGFR1 signaling pathway in CNV remains controversial. For example, one study reports that CNV is inhibited by oral administration of antibodies, gene knockdown, or inhibition of VEGFR1 signaling by siRNA. In another study, activation of VEGFR1 by VEGF or placental growth factor 1 (PIGF1), a ligand of VEGFR2, activates CNV in the eye via activation of VEGFR2 by SPARC. Yes. On the other hand, regarding VEGFR2, the knowledge that CNV proliferation is promoted by activation of VEGFR2 signaling is generally accepted.

Recently, a plurality of peptide fragments derived from VEGFR1 or VEGFR2 having the ability to induce cytotoxic T cells (CTL) have been identified, and it has been reported that these peptides have angiogenesis inhibitory effect (Patent Document 1- 2, Non-Patent Document 20). It has also been reported that these peptides are effective for the treatment of diseases mediated by angiogenesis such as tumors (Non-patent Document 21) and macular degeneration (Patent Documents 3-4).

WO2004 / 024766 WO2006 / 093030 WO2008 / 099908 WO2010 / 143435

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The present invention relates to peptides that induce cytotoxic T cells (CTLs) against endothelial cells that endogenously express VEGFR1. When these peptides are presented on antigen-presenting cells (APCs) by HLA antigens, CTLs having cytotoxic activity specific to VEGFR1-expressing cells are induced. As described in detail below, peripheral blood mononuclear cells (PBMC) obtained from healthy donors are stimulated with a VEGFR1-derived HLA-A ^* 0201 binding candidate peptide. Thereafter, a CTL line having specific cytotoxicity against HLA-A02 positive target cells pulsed with each candidate peptide is established. These results demonstrate that these peptides are HLA-A02 restricted epitope peptides that can induce a strong and specific immune response against cells expressing VEGFR1.

  Accordingly, it is an object of the present invention to provide an isolated VEGFR1-derived immunogenic peptide that binds to an HLA antigen. These peptides are predicted to be capable of inducing CTL and can therefore be used to induce CTL ex vivo or for administration to a subject for the purpose of inducing an immune response against vascular endothelial cells expressing VEGFR1 Can be used. Preferred peptides are nonapeptides or decapeptides, more preferably those having an amino acid sequence selected from among SEQ ID NOs: 1-153.

  The peptide of the present invention may be a peptide in which one, two, or more amino acids are substituted, deleted, inserted and / or added as long as the resulting modified peptide retains the original ability to induce CTL. Include.

  The present invention also provides an isolated polynucleotide encoding any one of the peptides of the present invention. These polynucleotides can be used to induce APCs that have the ability to induce CTL, or administered to a subject to induce an immune response against vascular endothelial cells that express VEGFR1, in much the same way as the peptides of the present invention. can do.

  When administered to a subject, the peptides of the invention are presented on the surface of the APC, thereby inducing CTL targeting the peptide. Accordingly, it is a further object of the present invention to provide a composition that induces CTL, comprising one or more peptides of the present invention or a polynucleotide encoding the peptide. The present invention further provides one or more peptides of the present invention or such peptides formulated for the treatment and / or prevention of diseases mediated by angiogenesis and the prevention of their recurrence after surgery A pharmaceutical composition comprising one or more polynucleotides encoding is provided.

  A method for inducing APC having the ability to induce CTL, comprising contacting APC with one or more peptides of the present invention, or introducing a polynucleotide encoding any one of the peptides of the present invention into APC It is a further object of the present invention to provide a method comprising the steps of:

  The present invention also comprises a step of co-culturing a CD8-positive T cell with APC that presents a complex of the HLA antigen and the peptide of the present invention on its surface; Co-cultured with exosomes presenting the complex with exosomes on their surface, or each T cell receptor (TCR) subunit capable of binding to the peptide of the invention presented by the HLA antigen on the cell surface Provided is a method for inducing CTL comprising the step of introducing a vector containing the encoding polynucleotide into CD8-positive T cells.

  It is yet another object of the present invention to provide an isolated APC that presents a complex of HLA antigen and a peptide of the present invention on its surface. The invention further provides an isolated CTL that targets the peptide of the invention. These APCs and CTLs can be used for immunotherapy against diseases mediated by angiogenesis.

  A method for inducing an immune response against vascular endothelial cells expressing VEGFR1 in a subject, comprising the step of administering to the subject a composition comprising the peptide of the present invention or a polynucleotide encoding the peptide. Is another object of the present invention.

  In addition to the foregoing, other objects and features of the invention will become more fully apparent when the following detailed description is read in conjunction with the accompanying figures and examples. However, it is to be understood that both the foregoing summary of the invention and the following detailed description are exemplary embodiments, and are not restrictive of the invention or other alternative embodiments of the invention. In particular, while the invention is described herein with reference to certain specific embodiments, it is understood that the description is illustrative of the invention and is not to be construed as limiting the invention. Like. Various modifications and applications can occur to those skilled in the art without departing from the spirit and scope of the invention as described by the appended claims. Similarly, other objects, features, benefits and advantages of the present invention will become apparent from the present summary and specific embodiments described below and will be readily apparent to those skilled in the art. Such objectives, features, benefits and advantages can be found in the accompanying examples, data, charts, and references incorporated by reference herein, either alone or in combination with any reasonable inferences drawn from them. It will be clear in consideration.

DESCRIPTION OF EMBODIMENTS Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of embodiments of the present invention, the preferred methods, devices, and materials are described herein. It describes. However, prior to describing the materials and methods of the present invention, the specific sizes, shapes, dimensions, materials, methodologies, protocols, etc. described herein may vary according to routine experimentation and optimization. As such, it should be understood that the invention is not limited thereto. The terminology used in the description is for the purpose of describing particular types or embodiments only, and is not intended to limit the scope of the invention which is limited only by the appended claims. It should also be understood.

I. Definitions As used herein, the words “one” and “that” mean “at least one” unless specifically stated otherwise.

  The terms “polypeptide”, “peptide”, and “protein” are used interchangeably herein and refer to a polymer of amino acid residues. The term refers to amino acid polymers in which one or more amino acid residues are modified or are non-natural residues such as artificial chemical mimetics of the corresponding natural amino acids, as well as natural amino acids Applied to polymer.

  As used herein, the term “amino acid” refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids. Natural amino acids are those encoded by the genetic code and amino acids that are post-translationally modified in cells (eg, hydroxyproline, γ-carboxyglutamic acid, and O-phosphoserine). The phrase “amino acid analog” has the same basic chemical structure as a natural amino acid (hydrogen, carboxy group, amino group, and alpha carbon attached to the R group), but has a modified R group or modified backbone. Refers to a compound (eg, homoserine, norleucine, methionine, sulfoxide, methionine methylsulfonium). The phrase “amino acid mimetic” refers to a compound that has a structure that is different from a common amino acid but that has a similar function.

  Amino acids may be referred to herein by generally known three letter symbols or by one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission.

  The terms “gene”, “polynucleotide”, “oligonucleotide”, and “nucleic acid” are used interchangeably herein and are referred to by the generally accepted one-letter code unless otherwise noted. .

  As used herein, the term “composition” is intended to encompass a product containing a specific amount of a specific component and any product that results directly or indirectly from a combination of a specific amount of a specific component. The Such term for a pharmaceutical composition is one from a product comprising an active ingredient and an inert ingredient that constitutes a carrier, as well as a combination, complexation or aggregation of any two or more ingredients. Alternatively, it is intended to encompass any product that results directly or indirectly from the dissociation of multiple components or from other types of reactions or interactions of one or more components. Accordingly, the pharmaceutical compositions of the present invention encompass any composition made by admixing a compound of the present invention and a pharmaceutically or physiologically acceptable carrier. As used herein, the phrase “pharmaceutically acceptable carrier” or “physiologically acceptable carrier” includes liquid or solid extenders, diluents, excipients, solvents, or encapsulating materials. It means a pharmaceutically or physiologically acceptable material, composition, substance, or vehicle that is not limited thereto.

  Unless otherwise indicated, the term “disease mediated by angiogenesis” refers to a disease in which angiogenesis is involved in the development and / or progression of the disease, examples of which are related to angiogenesis in various cancers and choroids. Diseases (neovascular macular disease: age-related macular degeneration, myopic macular degeneration, retinitis pigmentosa, central exudative chorioretinopathy, various retinitis pigmentosa, choroidal atrophy, choroideremia, choroidal osteoma Etc.), diabetic retinopathy, rheumatoid arthritis, psoriasis, and atherosclerosis. More specifically, it refers to a disease mediated by angiogenesis involving the expression of the VEGFR1 gene. At the diseased sites of these diseases, the VEGFR1 gene is expressed in vascular endothelial cells.

  Unless otherwise specified, the terms “cytotoxic T lymphocyte”, “cytotoxic T cell”, and “CTL” are used interchangeably herein and, unless otherwise specified, non-self cells ( For example, it refers to a sub-group of T lymphocytes that can recognize tumor / cancer cells, virus-infected cells) and induce the death of such cells.

Unless otherwise noted, the term “HLA-A02” refers to HLA-A ^* 0201 and HLA-A ^*
Refers to the HLA-A02 type including subtypes such as 0206.

  As long as the methods and compositions of the invention are useful in the context of a “treatment” of a disease mediated by angiogenesis, such as cancer, treatment may reduce the expression of the VEGFR1 gene, inhibit angiogenesis, or A treatment is considered “effective” if it provides a clinical benefit, such as a reduction in the symptoms of a disease mediated by angiogenesis. When the treatment is applied prophylactically, “effective” means that the treatment delays or prevents the onset of the disease or prevents or alleviates the clinical symptoms of the disease. Efficacy is determined in connection with any known method for diagnosing or treating a particular disease type. As long as the methods and compositions of the invention are useful in the context of “prevention” of diseases mediated by angiogenesis, the term “prevention” is used herein to reduce the mortality or morbidity burden due to the disease. Including any work to be made. Prevention can take place at “primary, secondary, and tertiary prevention levels”. Primary prevention avoids the development of disease, whereas secondary and tertiary level prevention, in addition to preventing disease progression and the appearance of symptoms, restores function and is disease-related Including the aim of reducing the adverse effects of existing diseases by reducing the complications of Alternatively, prophylaxis can include a wide range of prophylactic treatment aimed at reducing the severity of a particular disorder, eg, reducing tumor growth and metastasis.

  In the context of the present invention, cancer treatment and / or prevention and / or prevention of its recurrence after surgery includes the following stages: surgical excision of cancer cells, inhibition of cancer cell growth, tumor regression Or any of the stages such as regression, induction of remission and suppression of cancer development, tumor regression, and reduction or inhibition of metastasis. Effective treatment and / or prevention of cancer reduces mortality, improves the prognosis of individuals with cancer, decreases the level of tumor markers in the blood, and detectable symptoms associated with cancer To ease. For example, symptom relief or amelioration constitutes effective treatment and / or prevention, including 10%, 20%, 30%, or more relief or symptom stability.

  In the context of the present invention, the term “antibody” refers to immunoglobulins and fragments thereof that specifically react with the designated protein or peptide thereof. Antibodies can include human antibodies, primatized antibodies, chimeric antibodies, bispecific antibodies, humanized antibodies, antibodies fused with other proteins or radiolabels, and antibody fragments. Furthermore, in the present specification, “antibody” is used in a broad sense, specifically, an intact monoclonal antibody, a polyclonal antibody, a multispecific antibody formed from two or more intact antibodies (for example, a bispecific antibody). And antibody fragments as long as they exhibit the desired biological activity. “Antibody” refers to all classes (eg, IgA, IgD, IgE, IgG, and IgM).

  Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.

II. peptide
To demonstrate that VEGFR1-derived peptides function as antigens recognized by CTL, peptides from VEGFR1 (SEQ ID NO: 155) were analyzed and they were analyzed by HLA-A02, which is a commonly found HLA allele. It was determined whether it was a constrained antigen epitope (Date Y et al., Tissue Antigens 47: 93-101, 1996; Kondo A et al., J Immunol 155: 4307-12, 1995; Kubo RT et al. , J Immunol 152: 3913-24, 1994).

  VEGFR1-derived HLA-A02 binding peptides candidates were identified based on their binding affinity for HLA-A02. The candidate peptide is a peptide having an amino acid sequence selected from SEQ ID NOs: 1 to 153.

  In vitro stimulation of T cells by dendritic cells (DC) pulsed with these peptides can establish CTLs with cytotoxic activity specific for these peptides. Established CTLs show specific cytotoxic activity against target cells pulsed with each peptide.

  The VEGFR1 gene is a good target for immunotherapy because it is strongly expressed in vascular endothelial cells at the disease site in diseases mediated by angiogenesis, but is not expressed in most normal organs. Therefore, the present invention provides a nonapeptide (a peptide consisting of 9 amino acid residues) and a decapeptide (a peptide consisting of 10 amino acid residues) corresponding to the VEGFR1-derived epitope recognized by CTL. Particularly preferred examples of the nonapeptide and decapeptide of the present invention include peptides having an amino acid sequence selected from SEQ ID NOs: 1 to 153. Further preferred examples include peptides consisting of an amino acid sequence selected from SEQ ID NOs: 1 to 153.

Generally, Parker KC et al., J Immunol 1994 Jan
1, 152 (1): 163-75 and Nielsen M et al., Protein Sci 2003;
12: Calculate the binding affinity between various peptides and HLA antigens in silico using, for example, software programs currently available on the Internet, such as the software program described in 1007-17. it can. For example, Lafuente EM et
al., Current Pharmaceutical Design, 2009, 15, 3209-3220 etc. Parker KC et al., J Immunol 1994 Jan 1, 152 (1): 163-75, Kuzushima K et al., Blood 2001, 98 (6): 1872-81, Larsen MV et al. BMC Bioinformatics. 2007 Oct 31; 8: 424, Buus S et al. Tissue Antigens., 62: 378-84, 2003, Nielsen M et al., Protein Sci 2003; 12: 1007-17, and Nielsen M et al. PLoS ONE 2007; 2: e796 and Lin
The binding affinity with the HLA antigen can be measured as described in HH et al. BMC Immunol. 2008 Mar 16; 9: 8. Methods for determining binding affinity are described, for example, in Journal of Immunological Methods, 1995, 185: 181-190; Protein Science, 2000, 9: 1838-1846. Thus, such software programs can be used to select VEGFR1-derived fragments that have a high binding affinity for HLA. Accordingly, the present invention encompasses a peptide composed of any fragment derived from VEGFR1 that is determined to bind to an HLA antigen by such a known program. Furthermore, such peptides may include peptides consisting of full length VEGFR1.

  The nonapeptides and decapeptides of the present invention can be flanked by additional amino acid residues as long as the resulting peptide retains its ability to induce CTL. Additional amino acid residues can be composed of any type of amino acid as long as they do not impair the ability of the original peptide to induce CTL. Accordingly, the present invention encompasses peptides having binding affinity for HLA antigens, including peptides derived from VEGFR1. Such peptides are, for example, less than about 40 amino acids, often less than about 20 amino acids, and usually less than about 15 amino acids.

  In general, modification of one, two, or more amino acids in a peptide does not affect the function of the peptide and in some cases even enhances the desired function of the original peptide. Indeed, a modified peptide (ie, one, two, or a few amino acid residues were modified (ie, substituted, deleted, inserted and / or added) compared to the original reference sequence) Peptides composed of amino acid sequences) are known to retain the biological activity of the original peptide (Mark et al., Proc Natl Acad Sci USA 1984, 81: 5662-6; Zoller and Smith, Nucleic Acids Res 1982, 10: 6487-500; Dalbadie-McFarland et al., Proc Natl Acad Sci USA 1982, 79: 6409-13). Thus, in one embodiment, the peptides of the invention have one, two or more amino acids substituted, deleted, inserted and / or added in an amino acid sequence selected from among SEQ ID NOs: 1-153. And a peptide having an ability to induce CTLs.

One skilled in the art can recognize individual substitutions to an amino acid sequence that alter a single amino acid or a small percentage of amino acids that tend to conserve the properties of the original amino acid side chain. Thus, they are often referred to as “conservative substitutions” or “conservative modifications”, where a change in the protein results in a modified protein having a similar function to the original protein. Conservative substitution tables providing functionally similar amino acids are well known in the art. Examples of amino acid side chain properties that are desirable to preserve include, for example, hydrophobic amino acids (A, I, L, M, F, P, W, Y, V), hydrophilic amino acids (R, D, N, C, E, Q, G, H, K, S, T), as well as side chains having the following functional groups or characteristics in common: aliphatic side chains (G, A, V, L, I, P); hydroxyl group-containing side chains (S, T, Y); sulfur atom-containing side chains (C, M); carboxylic acid and amide-containing side chains (D, N, E, Q); base-containing side chains (R) , K, H); and aromatic-containing side chains (H, F, Y, W). In addition, the following eight groups each contain amino acids recognized in the art as conservative substitutions for each other:
1) Alanine (A), Glycine (G);
2) Aspartic acid (D), glutamic acid (E);
3) Asparagine (N), glutamine (Q);
4) Arginine (R), Lysine (K);
5) Isoleucine (I), leucine (L), methionine (M), valine (V);
6) phenylalanine (F), tyrosine (Y), tryptophan (W);
7) serine (S), threonine (T); and
8) Cysteine (C), methionine (M) (see, for example, Creighton, Proteins 1984).

  Such conservatively modified peptides are also encompassed by the peptides of the present invention. However, the peptide of the present invention is not limited to these, and may contain non-conservative modifications as long as the modified peptide retains the CTL-inducing ability of the original peptide. Furthermore, the modified peptides do not exclude polymorphic variants of VEGFR1, interspecies homologues, and allele-derived CTL inducible peptides.

  A small number (eg, one, two, or several) or a small percentage of amino acids can be modified (substitutions, deletions, insertions and / or additions) as long as they retain the required CTL inducibility it can. As used herein, the term “several” means 5 or fewer amino acids, such as 4 or 3 or fewer. The percentage of amino acids to be modified is preferably 20% or less, more preferably 15% or less, even more preferably 10% or less, or 1 to 5%.

When used in the context of immunotherapy, the peptides of the invention should be presented on the surface of cells or exosomes, preferably as a complex with HLA antigens. Therefore, it is preferable to select a peptide that not only induces CTL but also has a high binding affinity for the HLA antigen. To that end, peptides can be modified by substitution, deletion, insertion and / or addition of amino acid residues to obtain modified peptides with improved binding affinity. In addition to naturally presented peptides, the regularity of the sequence of peptides presented by binding to HLA antigens is known (J
Immunol 1994, 152: 3913; Immunogenetics 1995, 41: 178; J Immunol 1994, 155: 4307), modifications based on such regularity can be introduced into the immunogenic peptides of the present invention.

  For example, to increase HLA-A02 binding affinity, it may be desirable to replace the second amino acid from the N-terminus with leucine or methionine and / or the C-terminal amino acid with valine or leucine. There is. Accordingly, the second amino acid from the N-terminal of the amino acid sequence selected from SEQ ID NOs: 1 to 153 is substituted with leucine or methionine, and / or the amino acids selected from SEQ ID NOs: 1 to 153 Peptides comprising an amino acid sequence in which the C-terminus of the sequence is substituted with valine or leucine are encompassed by the present invention. In a preferred embodiment, the peptide of the present invention is such that the second amino acid from the N-terminus of the amino acid sequence selected from SEQ ID NOs: 1 to 153 is substituted with leucine or methionine, and / or SEQ ID NOs: 1 to It may be a peptide consisting of an amino acid sequence in which the C-terminus of the amino acid sequence selected from 153 is substituted with valine or leucine.

Substitutions can be introduced not only at the terminal amino acids but also at the potential T cell receptor (TCR) recognition site of the peptide. Some studies have shown that peptides with amino acid substitutions are comparable to the original, such as CAP1, p53 _(264-272) , Her-2 / neu _(369-377) , or gp100 _(209-217) Or prove that it can be better (Zaremba et al. Cancer
Res. 57, 4570-4577, 1997, T.
K. Hoffmann et al. J Immunol. (2002) Feb 1; 168 (3): 1338-47., SO Dionne et al. Cancer Immunol immunother. (2003) 52: 199-206, and SO Dionne et al. Cancer Immunology, Immunotherapy (2004) 53,
307-314).

  The present invention also contemplates that the addition of one, two, or several amino acids can also be added to the N-terminus and / or C-terminus of the peptides of the present invention. Such modified peptides having high HLA antigen binding affinity and retaining CTL inducibility are also included in the present invention.

  However, if the peptide sequence is identical to part of the amino acid sequence of an endogenous or exogenous protein with different functions, side effects such as autoimmune disorders and / or allergic symptoms to certain substances may be induced. is there. Therefore, in order to avoid the situation where the peptide sequence matches the amino acid sequence of another protein, it is preferable to first perform a homology search using an available database. If the homology search reveals that there is not even a peptide that differs by one or two amino acids compared to the peptide of interest, without the risk of such side effects, The peptide of interest can be modified to increase its binding affinity and / or to increase its ability to induce CTLs.

  Peptides with high binding affinity for HLA antigens are expected to be very effective as described above, but candidate peptides selected using the presence of high binding affinity as an index are used for the presence or absence of CTL inducibility. Check further. As used herein, the phrase “CTL inducibility” refers to the ability of a peptide to induce cytotoxic T cells (CTL) when presented on antigen presenting cells (APC). Furthermore, “CTL inducibility” includes the ability of a peptide to induce CTL activation, induce CTL proliferation, promote lysis of target cells by CTL, and increase IFN-γ production of CTL.

Confirmation of the ability to induce CTLs induces APC (eg, B lymphocytes, macrophages, and dendritic cells (DC)) carrying human MHC antigens, or more specifically DCs derived from human peripheral blood mononuclear leukocytes. After stimulation with peptide, mixing with CD8 positive T cells and then measuring IFN-γ released by CTL against target cells. As a reaction system, a transgenic animal prepared to express human MHC antigen (HLA antigen) (for example, BenMohamed L, Krishnan R, Longmate J, Auge C, Low L, Primus J,
Diamond DJ, Hum Immunol 2000 Aug, 61 (8): 764-79, Related Articles, Books,
Linkout Induction of CTL response by a minimal epitope vaccine in HLA A ^* 0201 / DR1
transgenic mice: dependence on HLA class II restricted T (H) response) can be used. For example, the target cell can be radiolabeled with ⁵¹ Cr or the like, and the cytotoxic activity can be calculated from the radioactivity released from the target cell. Alternatively, by measuring the IFN-γ produced and released by CTL in the presence of APC carrying the immobilized peptide and visualizing the inhibition zone on the medium using anti-IFN-γ monoclonal antibody, CTL Inducibility can be evaluated.

  Furthermore, from the results of homology analysis, it can be confirmed whether these peptides have significant homology with peptides derived from any other known human gene products. This can reduce the likelihood of an unknown or undesirable immune response when used in immunotherapy. Thus, also from this aspect, these peptides can be used to induce immunity against VEGFR1 in patients.

In addition to the above modifications, the peptides of the present invention can be linked to other peptides as long as the resulting linked peptide retains the required CTL inducibility of the original peptide. Examples of suitable peptides include the peptides of the present invention or CTL inducible peptides derived from tumor associated antigens (TAA). Suitable linkers between peptides are well known in the art and include, for example, AAY (PM Daftarian et al., J Trans Med
2007, 5:26), AAA, NKRK (RPM Sutmuller et al., J Immunol. 2000, 165: 7308-7315), or K (S. Ota et al., Can Res. 62, 1471-1476, KS
Kawamura et al., J Immunol. 2002, 168: 5709-5715).

  For example, tumor-associated antigenic peptides can be used substantially simultaneously to increase the immune response via HLA class I and / or class II against cancer cells. It is well established that cancer cells can express more than one tumor-related gene. Thus, determining whether a particular subject expresses a particular tumor associated gene, and subsequently in a VEGFR1 composition or vaccine according to the invention, HLA class I and / or derived from the expression product of such gene Or including HLA class II binding peptides is within the routine experimentation of one of ordinary skill in the art.

  Also, HLA class I and / or HLA class II derived from other VEGF receptors such as VEGFR2 to increase immune response via HLA class I and / or class II against vascular endothelial cells involved in angiogenesis Binding peptides can also be used substantially simultaneously. Such peptides can also be included in the VEGFR1 compositions or vaccines of the invention.

  Examples of HLA class I and HLA class II binding peptides are known to those skilled in the art (see, eg, Coulie, Stem Cells 13: 393-403, 1995) and in a manner similar to that disclosed herein. It can be used in the present invention. Accordingly, one of ordinary skill in the art can use a standard procedure in molecular biology to convert a polypeptide comprising one or more VEGFR1 peptides and one or more of the non-VEGFR1 peptides, or a nucleic acid encoding such a polypeptide, to molecular biology. And can be easily prepared.

  Such a linking peptide as described above is referred to herein as a “polytope”, that is, two or more potential immunogenicities that can be linked in various configurations (eg, linked, overlapping). Or a group of immune response stimulating peptides. A polytope (or nucleic acid encoding the polytope) can be administered to a standard immunization protocol, for example, to an animal to test the effectiveness of the polytope in promoting, enhancing, and / or inducing an immune response.

  Peptides can be linked directly or by use of linker sequences to form polytopes, and the use of polytopes as vaccines is well known in the art (eg, Thomson et al., Proc. Natl. Acad Sci USA 92 (13): 5845-5849, 1995; Gilbert et al., Nature Biotechnol. 15 (12): 1280-1284, 1997; Thomson et al., J Immunol. 157 (2): 822-826, 1996; see Tarn et al., J Exp. Med. 171 (1): 299-306, 1990). Polytopes containing various numbers and combinations of epitopes can be prepared and tested for recognition by CTLs and for efficacy in increasing immune responses.

  The peptides of the invention can also be linked to other substances so long as the resulting linking peptide retains the necessary CTL inducing ability of the original peptide. Examples of suitable materials include, for example, peptides, lipids, sugars and sugar chains, acetyl groups, natural and synthetic polymers, and the like. A peptide can include modifications such as glycosylation, side chain oxidation, or phosphorylation, as long as the modification does not compromise the biological activity of the original peptide. Such types of modifications can be made to provide additional functions (eg, targeting and delivery functions) or to stabilize the peptide.

  For example, it is known in the art to introduce D-amino acids, amino acid mimetics, or unnatural amino acids to increase the in vivo stability of the peptides, and this concept can also be adapted to the peptides of the present invention. . Peptide stability can be assayed in several ways. For example, peptidases and various biological media such as human plasma and serum can be used to test stability (see, eg, Verhoef et al., Eur J Drug Metab Pharmacokin 1986, 11: 291-302). I want to be)

Further, as described above, among the modified peptides that are substituted, deleted, inserted and / or added by one, two, or several amino acid residues, the same as or compared to the original peptide Those having higher activity can be screened or selected. Accordingly, the present invention also provides a method for screening or selecting for a modified peptide having the same or higher activity compared to the original. An exemplary method includes the following steps:
a: substituting or deleting at least one amino acid residue of the peptide of the present invention, and / or adding or inserting at least one amino acid residue to the peptide of the present invention,
b: determining the activity of the peptide produced in step a,
c: selecting a peptide having the same or higher activity compared to the activity of the original peptide.

  The activity determined in the above step b can include HLA binding activity, APC or CTL inducing ability, and immunity inducing activity in vivo.

  Herein, the peptides of the present invention are also described as “VEGFR1 peptides” or “VEGFR1 polypeptides”.

III. Preparation of VEGFR1 peptides The peptides of the present invention can be prepared using well-known techniques. For example, the peptides of the invention can be prepared using recombinant DNA technology or chemical synthesis. The peptides of the present invention can be synthesized individually or as longer polypeptides comprising two or more peptides. The peptide of the invention can then be isolated from the host cell or the synthesis reaction. That is, the peptides of the invention can be purified or isolated so that they are substantially free of other natural host cell proteins and fragments thereof, or any other chemicals.

  The peptide of the present invention may contain modifications such as glycosylation, side chain oxidation, or phosphorylation as long as the modification does not impair the biological activity of the original peptide. Other exemplary modifications include the incorporation of D-amino acids or other amino acid mimetics that can be used, for example, to increase the serum half-life of the peptide.

The peptide of the present invention can be obtained by chemical synthesis based on the selected amino acid sequence. Examples of conventional peptide synthesis methods that can be adapted for the synthesis include those described in the literature as follows:
(I) Peptide Synthesis, Interscience, New York, 1966;
(Ii) The Proteins, Vol. 2, Academic Press, New York,
1976;
(Iii) “Peptide Synthesis” (Japanese), Maruzen, 1975;
(Iv) “Basics and Experiments of Peptide Synthesis” (Japanese), Maruzen,
1985;
(V) “Development of follow-up drugs” (Japanese), Volume 14 (peptide synthesis),
Hirokawa Shoten, 1991;
(Vi) WO99 / 67288; and (vii) Barany G. & Merrifield RB, Peptides Vol. 2,
Solid Phase Peptide Synthesis, Academic Press, New York, 1980, 100-118.

  Alternatively, any known genetic engineering method for producing peptides can be adapted to obtain the peptides of the invention (eg Morrison J, J Bacteriology 1977, 132: 349-51; Clark-Curtiss & Curtiss, Methods in Enzymology (Edited by Wu et al.) 1983, 101: 347-62). For example, first, an appropriate vector having a polynucleotide encoding the peptide of interest in a form that can be expressed (eg, downstream of a regulatory sequence corresponding to a promoter sequence) is prepared and transformed into an appropriate host cell. The host cell is then cultured to produce the peptide of interest. Peptides can also be generated in vitro using an in vitro translation system.

IV. Polynucleotides The present invention also provides polynucleotides that encode any of the aforementioned peptides of the present invention. These include the natural VEGFR1 gene (GenBank accession numbers NM_002019.4, NM_001159920.1,
NM_001160030.1,
Polynucleotides derived from NM — 001160031.1, (eg, SEQ ID NO: 154), and polynucleotides having conservatively modified nucleotide sequences thereof. As used herein, the phrase “conservatively modified nucleotide sequence” refers to sequences that encode the same or essentially the same amino acid sequence. Because of the degeneracy of the genetic code, a large number of functionally identical nucleic acids encode any particular protein. For example, the codons GCA, GCC, GCG, and GCU all encode the amino acid alanine. Thus, at any position where an alanine is specified by a codon, the codon can be changed to any of the corresponding codons described without altering the encoded polypeptide. Such nucleic acid mutations are “silent mutations” and are a type of mutation conservatively modified. Every nucleic acid sequence herein that encodes a peptide also represents every possible silent variation of the nucleic acid. Those skilled in the art will be able to modify each codon in the nucleic acid (except AUG, which is usually the only codon for methionine, and TGG, which is usually the only codon for tryptophan) to obtain a functionally identical molecule. You will recognize. Accordingly, each silent variation of a nucleic acid that encodes a peptide is implicitly described in each disclosed sequence.

  The polynucleotide of the present invention can be composed of DNA, RNA, and derivatives thereof. DNA is appropriately composed of bases such as A, T, C, and G, and in RNA, T is replaced with U.

  A polynucleotide of the present invention may encode a plurality of peptides of the present invention with or without intervening amino acid sequences in between. For example, the intervening amino acid sequence can provide a cleavage site (eg, an enzyme recognition sequence) for the polynucleotide or translated peptide. Furthermore, the polynucleotide may comprise any additional sequence to the coding sequence that encodes a peptide of the invention. For example, the polynucleotide may be a recombinant polynucleotide containing regulatory sequences necessary for expression of the peptide, or may be an expression vector (plasmid) having a marker gene or the like. In general, such recombinant polynucleotides can be prepared, for example, by manipulating the polynucleotide by conventional recombinant techniques using polymerases and endonucleases.

The polynucleotides of the present invention can be produced using either recombinant techniques or chemical synthesis techniques. For example, a polynucleotide can be made by inserting into an appropriate vector, which can be expressed when transfected into competent cells. Alternatively, polynucleotides can be amplified using PCR techniques or expression in an appropriate host (eg, Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring
(See Harbor Laboratory, New York, 1989). Or Beaucage
SL & Iyer RP, Tetrahedron 1992, 48: 2223-311; Matthes
Polynucleotides can also be synthesized using the solid phase technique described in et al., EMBO J 1984, 3: 801-5.

V. Exosomes The present invention further provides intracellular vesicles, called exosomes, that present complexes formed between the peptides of the present invention and HLA antigens on their surface. Exosomes can be prepared using, for example, the methods described in detail in Japanese Patent Publication No. 11-510507 and WO99 / 03499, and APC obtained from a patient to be treated and / or prevented can be prepared. Can be prepared. The exosomes of the present invention can be vaccinated as a vaccine in the same manner as the peptides of the present invention.

The type of HLA antigen contained in the complex must match that of the subject in need of treatment and / or prevention. For example, in the Japanese population, HLA-A02, especially HLA-A ^* 0201 and HLA-A ^* 0206 are widely prevalent and are therefore considered suitable for the treatment of Japanese patients. The use of type A02 that is highly expressed between Japanese and Caucasians is preferred for obtaining effective results, and subtypes such as HLA-A ^* 0201 and HLA-A ^* 0206 are also used. Typically, peptides that have a high level of binding affinity for a particular antigen or have the ability to induce CTLs by antigen presentation by pre-examining the type of HLA antigen of the patient in need of treatment at the clinic Appropriate selection is possible. Further, in order to obtain a peptide having both high binding affinity and CTL inducing ability, one, two, or several amino acid substitutions, deletions, based on the amino acid sequence of the natural VEGFR1 partial peptide, Insertions and / or additions can be made.

  When the A02 type HLA antigen is used for the exosome of the present invention, a peptide having an amino acid sequence selected from SEQ ID NOs: 1 to 153 is used.

VI. Antigen presenting cell (APC)
The present invention also provides an isolated antigen presenting cell (APC) that presents on its surface the complex formed between the HLA antigen and the peptide of the present invention. APC may be derived from a patient to be treated and / or prevented and administered as a vaccine alone or in combination with other drugs, including peptides, exosomes, or CTLs of the present invention. it can.

  The APC is not limited to a particular type of cell, including dendritic cells (DCs) known to present proteinaceous antigens on their cell surface as recognized by lymphocytes, Langerhans cells, macrophages, B cells, and activated T cells are included. Since DC is a representative APC having the strongest CTL inducing action among APCs, DC can be preferably used as the APC of the present invention.

  For example, the APCs of the invention can be obtained by inducing DCs from peripheral blood monocytes and then stimulating them with the peptides of the invention in vitro, ex vivo, or in vivo. When the peptide of the present invention is administered to a subject, APC presenting the peptide of the present invention is induced in the subject's body. The phrase “inducing APC” refers to stimulating a cell with a peptide of the present invention or a nucleotide encoding the peptide of the present invention to form a complex formed between the HLA antigen and the peptide of the present cell. Including presenting on the surface. Therefore, the APC of the present invention can be obtained by administering the peptide of the present invention to a subject and then recovering the APC from the subject. Alternatively, the APC of the present invention can be obtained by contacting APC recovered from a subject with the peptide of the present invention.

In a subject, the APC of the invention is administered to the subject alone or in combination with other agents including peptides, exosomes, or CTLs of the invention to induce an immune response against vascular endothelial cells that express VEGFR1 can do. For example, ex vivo administration may include the following steps:
a: recovering APC from the first subject;
b: contacting the APC of step a with a peptide; and
c: administering the bpc of step b to a second subject.

  The first subject and the second subject may be the same individual or different individuals. When the first object and the second object are different individuals, the HLA of the first object and the second object is preferably the same. The APC obtained by step b above can be a vaccine for treating and / or preventing diseases mediated by angiogenesis.

  The present invention also provides use of the peptide of the present invention for producing a pharmaceutical composition for inducing antigen-presenting cells. In addition, the present invention provides a method or process for producing a pharmaceutical composition that induces antigen-presenting cells. Furthermore, the present invention also provides a peptide of the present invention for inducing antigen-presenting cells.

The APC of the present invention obtained by the method as described above has a high level of CTL inducing ability. The high level in the term “high level of CTL inducibility” is compared to the level of CTL inducibility by APC that has not been contacted with a peptide or APC that has been contacted with a peptide that cannot induce CTL. . Such an APC having a high level of CTL inducibility can be prepared by a method including the step of introducing a polynucleotide encoding the peptide of the present invention into APC in vitro in addition to the above method. The polynucleotide to be introduced may be in the form of DNA or RNA. Examples of introduction methods include, but are not limited to, various methods conventionally practiced in the art, such as lipofection, electroporation, and the calcium phosphate method. More specifically, Cancer Res 1996, 56: 5672-7; J Immunol 1998,
161: 5607-13; J Exp Med 1996, 184: 465-72; it can be performed as described in published patent publication 2000-509281. By introducing the gene into APC, the gene undergoes transcription, translation, etc. in the cell, and then the obtained protein is processed by MHC class I or class II, and the partial peptide of the present invention passes through the presentation pathway. Presented.

In a preferred embodiment, the APC of the present invention is an APC presenting a complex formed between HLA-A02 (more preferably HLA-A ^* 0201) and the peptide of the present invention on its cell surface. It is. Also, the APC of the present invention is preferably an APC derived by a method comprising the steps described in a or b below:
a: contacting APC expressing HLA-A02 (more preferably HLA-A ^* 0201) with the peptide of the present invention;
b: introducing a polynucleotide encoding the peptide of the present invention into APC expressing HLA-A02 (more preferably HLA-A ^* 0201).

VII. Cytotoxic T lymphocyte (CTL)
CTLs induced against any one of the peptides of the invention can be used as vaccines in a manner similar to the peptides themselves to enhance immune responses targeting vascular endothelial cells that express VEGFR1 in vivo. it can. Accordingly, the present invention provides an isolated CTL specifically induced or activated by any one of the peptides of the present invention.

  Such CTLs are (1) administered a peptide of the present invention to a subject, or (2) stimulated APC and CD8 positive T cells or peripheral blood mononuclear leukocytes derived from the subject with the peptide of the present invention in vitro. Or (3) contacting CD8 positive T cells or peripheral blood mononuclear leukocytes in vitro with APC or exosomes that present a complex of HLA antigen and said peptide on their surface, or (4) It can be obtained by introducing a vector comprising a polynucleotide encoding each subunit of the T cell receptor (TCR) capable of binding to the peptide of the present invention presented by the HLA antigen on the cell surface. The APC or exosome used in the method (2) or (3) can be prepared by the method described in the section “VI. Antigen-presenting cell (APC)”. Details are described below in the section “VIII. T Cell Receptor (TCR)”.

  The CTL of the present invention may be derived from a patient to be treated and / or prevented and is administered alone or with other drugs including the peptide of the present invention, APC or exosome for the purpose of modulating the effect. Can be administered in combination. The CTL of the present invention specifically acts on a target cell presenting the peptide of the present invention, for example, the same peptide used for induction of the CTL of the present invention. The target cell may be a cell that endogenously expresses VEGFR1, such as an endothelial cell of tumor tissue, or a cell transfected with the VEGFR1 gene, and the peptide is presented on the cell surface by stimulation with the peptide of the present invention. Cells can also be targeted by activated CTL attacks.

In a preferred embodiment, the CTLs of the present invention specifically target cells expressing both HLA-A02 (more preferably HLA-A ^* 0201) and VEGFR1. In addition, the CTL of the present invention preferably has a complex formed between HLA-A02 (more preferably HLA-A ^* 0201) displayed on the cell surface and the peptide of the present invention via TCR. CTL that can be combined. In addition, the CTL of the present invention is preferably a CTL induced by a method comprising the steps described in the following a or b:
a: contacting CD8 positive T cells in vitro with APC or exosomes presenting a complex of HLA-A02 (more preferably HLA-A ^* 0201) and a peptide of the invention on its surface;
b: a vector comprising a polynucleotide encoding each subunit of TCR capable of binding to the peptide of the present invention presented on CD8 positive T cells by HLA-A02 (more preferably HLA-A ^* 0201) on the cell surface Stage to introduce.

VIII. T cell receptor (TCR)
The present invention also includes a composition comprising a polynucleotide encoding each subunit of a T cell receptor (TCR) capable of binding to the peptide of the present invention presented by the HLA antigen on the cell surface, and a method of using the same I will provide a. The polynucleotide confers CD8 positive T cells with specificity for vascular endothelial cells expressing VEGFR1 by forming a TCR on the cell surface that can bind to the peptides of the present invention presented by the HLA antigen. By using known methods in the art, polynucleotides encoding α and β chains as TCR subunits of CTL induced by the peptides of the present invention can be identified (WO2007 / 032255, and Morgan et al., J Immunol,
171, 3288 (2003)). For example, the PCR method is preferable for analyzing TCR. PCR primers for analysis include, for example, a 5′-R primer (5′-gtctaccaggcattcgcttcat-3 ′) (SEQ ID NO: 156) as a 5 ′ primer, and a TCR α chain C region as a 3 ′ primer. Specific 3-TRa-C primer (5'-tcagctggaccacagccgcagcgt-3 ') (SEQ ID NO: 157), 3-TRb-C1 primer specific for TCRβ chain C1 region (5'-tcagaaatcctttctcttgac-3') (sequence) No. 158), or a 3-TRβ-C2 primer (5′-ctagcctctggaatcctttctctt-3 ′) (SEQ ID NO: 159) specific for the TCR β chain C2 region, but is not limited thereto. A TCR formed by introducing the identified polynucleotide into a CD8-positive T cell can bind with high binding force to a target cell presenting the peptide of the present invention, and presents the peptide of the present invention. Mediates efficient killing of target cells in vivo and in vitro.

  The polynucleotide encoding each subunit of the TCR can be incorporated into an appropriate vector, such as a retroviral vector. These vectors are well known in the art. The polynucleotide or a vector containing them in an expressible form can be introduced into a CD8-positive T cell, eg, a patient-derived CD8-positive T cell. Advantageously, the present invention provides for the rapid and easy generation of modified T cells with superior vascular endothelial cell killing properties by rapid modification of the patient's own T cells (or another mammalian T cell). Provide ready-made compositions that enable.

  In the present specification, the specific TCR specifically indicates a complex of the peptide of the present invention and the HLA antigen presented on the surface of a target cell when the TCR is present on the surface of a CD8-positive T cell. It is a TCR that can recognize and confer specific cytotoxic activity on target cells. Specific recognition of the complex can be confirmed by any known method, and preferred examples include HLA multimer staining analysis using HLA molecules and peptides of the present invention, and ELISPOT assay. By performing the ELISPOT assay, it can be confirmed that the T cell introduced with the polynucleotide specifically recognizes the target cell by TCR and that the signal is transmitted intracellularly. When the TCR is present on the surface of a CD8-positive T cell, confirmation that the TCR can impart a target cell-specific cytotoxic activity to the CD8-positive T cell is also performed by a known method. be able to. Preferred methods include measuring cytotoxic activity against target cells, such as by a chromium release assay.

  The present invention also transduces a polynucleotide encoding each subunit of TCR that binds to a VEGFR1 peptide, eg, a peptide having an amino acid sequence selected from SEQ ID NOs: 1-153 in the context of HLA-A02. CTLs prepared by the method are provided.

  Transduced CTL can be homed in vivo and can be propagated by well-known in vitro culture methods (eg, Kawakami et al., J Immunol., 142, 3452-3461 (1989)). The CTLs of the invention can be used to form immunogenic compositions useful for the treatment or prevention of disease in patients in need of treatment or prevention, the contents of which are hereby incorporated by reference. (See WO2006 / 031221).

IX. Pharmaceutical composition
VEGFR1 expression is elevated in vascular endothelial cells at disease sites in diseases mediated by angiogenesis compared to normal tissues. Therefore, the peptide of the present invention or a polynucleotide encoding the peptide can be used for treatment and / or prevention of a disease mediated by angiogenesis and / or prevention of its recurrence after surgery. Accordingly, the present invention provides a pharmaceutical composition for the treatment and / or prevention of a disease mediated by angiogenesis and / or prevention of its recurrence after surgery, comprising one kind of the peptide or polynucleotide of the present invention Or the composition which contains multiple types as an active ingredient is provided. Alternatively, the peptides of the invention can be expressed on the surface of any of the aforementioned exosomes or cells such as APC for use as a pharmaceutical composition. In addition, the above-mentioned CTL targeting any one of the peptides of the present invention can also be used as an active ingredient of the pharmaceutical composition of the present invention.

  The pharmaceutical composition of the present invention may also be used as a vaccine. In the context of the present invention, the phrase “vaccine” (also referred to as “immunogenic composition”) is a composition having the function of inducing an immune response that provides an anti-angiogenic effect when inoculated into an animal. Point to.

  The pharmaceutical compositions of the present invention are human, and not limited to mice, rats, guinea pigs, rabbits, cats, dogs, sheep, goats, pigs, cows, horses, monkeys, baboons, and chimpanzees, especially commercially important To treat and / or prevent a disease mediated by angiogenesis and / or to prevent its recurrence after surgery in a subject or patient comprising a non-human animal or any other mammal, including livestock Can do.

In another aspect, the present invention also provides the use of an active ingredient selected from among the following in the manufacture of a pharmaceutical composition for treating or preventing a disease mediated by angiogenesis:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

Alternatively, the present invention further provides an active ingredient selected from the following for use in the treatment or prevention of diseases mediated by angiogenesis:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

Alternatively, the present invention further provides a method or process for producing a pharmaceutical composition for treating or preventing a disease mediated by angiogenesis, comprising an active ingredient selected from the following: Or a method comprising the steps of formulating a physiologically acceptable carrier:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

In another aspect, the present invention also provides a method or process for producing a pharmaceutical composition for treating or preventing a disease mediated by angiogenesis, comprising an active ingredient selected from A method or process is provided that comprises mixing with a pharmaceutically or physiologically acceptable carrier:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

  In the examples disclosed herein, the peptide having an amino acid sequence selected from SEQ ID NOs: 1 to 153 is an HLA-A02 restricted epitope peptide or its peptide capable of inducing a strong and specific immune response. Identified as a candidate. Accordingly, the pharmaceutical composition of the present invention comprising at least one peptide having an amino acid sequence selected from among SEQ ID NOs: 1 to 153 is particularly suitable for administration to a subject having HLA-A02 as an HLA antigen. Yes. The same applies to pharmaceutical compositions comprising a polynucleotide encoding any of these peptides (ie, a polynucleotide of the present invention).

  Diseases to be treated and / or prevented by the pharmaceutical composition of the present invention are not particularly limited, and various cancers, diseases related to angiogenesis in the choroid (neovascular maculopathy: age-related macular degeneration, myopia) Macular degeneration, retinitis pigmentosa, central exudative retina choroidopathy, various retinal pigment epitheliopathy, choroidal atrophy, choroideremia, choroidal osteoma, etc.), diabetic retinopathy, rheumatoid arthritis, psoriasis, or atheroma Includes all types of angiogenesis-mediated diseases involving VEGFR1, including atherosclerosis and the like.

Angiogenesis at the tumor site is also closely associated with solid tumor growth and metastasis (Folkman, J. et al.
(1995) Nature Med. 1: 27-31; Bicknell et al., (1996) Curr. Opin. Oncol. 8: 60-5). Therefore, the pharmaceutical composition of the present invention can also be used to suppress the growth and / or metastasis of cancer (solid tumor).

  The pharmaceutical composition of the present invention comprises, in addition to the above-mentioned active ingredient, other peptides (for example, peptides derived from VEGFR2) having the ability to induce CTLs against vascular endothelial cells at disease sites, and others encoding the other peptides And other cells presenting the other peptides, and the like. In addition, when the pharmaceutical composition of the present invention is particularly for treating and / or preventing cancer, the pharmaceutical composition of the present invention has the ability to induce CTL against cancer cells. A peptide, a polynucleotide encoding the peptide, a cell presenting the peptide, and the like may be included. As used herein, other peptides having the ability to induce CTLs against cancer cells are exemplified by, but not limited to, cancer specific antigens (eg, identified TAAs).

  If necessary, the pharmaceutical composition of the present invention may optionally contain the therapeutic substance as an active ingredient unless the other therapeutic substance inhibits the anti-angiogenic effect of the active ingredient such as any of the peptides of the present invention. Can be included. For example, the pharmaceutical composition of the present invention may optionally include an anti-inflammatory composition, an analgesic, a chemotherapeutic agent and the like. In addition to including other therapeutic substances in the pharmaceutical composition itself of the present invention, the pharmaceutical composition of the present invention may also be administered sequentially or simultaneously with one or more other pharmaceutical compositions. it can. The dosage of the pharmaceutical composition of the present invention and other pharmaceutical compositions depends, for example, on the type of pharmaceutical composition used, the disease to be treated, and the schedule and route of administration.

  In addition to the ingredients specifically mentioned herein, it is understood that the pharmaceutical compositions of the invention may also contain other ingredients customary in the art in view of the type of formulation. Should.

  In one embodiment of the invention, the pharmaceutical composition of the invention can be included in a product or kit comprising materials useful for treating the condition of the disease to be treated, such as cancer. The product or kit can include a container containing any of the pharmaceutical compositions of the invention having a label. Suitable containers include bottles, vials, and test tubes. The container may be formed from a variety of materials such as glass or plastic. The label on the container should indicate that the pharmaceutical composition is used for the treatment or prevention of one or more conditions of the disease. The label may also indicate directions for administration and the like.

  The kit containing the pharmaceutical composition of the present invention may optionally further comprise a second container containing a pharmaceutically acceptable diluent in addition to the containers described above. It may further include other materials desirable from a commercial and user standpoint, including other buffers, diluents, filters, needles, syringes, and package inserts with instructions for use.

  If desired, the pharmaceutical compositions of the invention can be provided in packs or dispenser devices that may contain one or more unit dosage forms containing the active ingredients. The pack may include metal foil or plastic foil, such as a blister pack. The pack or dispenser device can be accompanied by instructions for administration.

(1) Pharmaceutical composition containing peptide as active ingredient The peptide of the present invention can be directly administered as the pharmaceutical composition of the present invention or, if necessary, formulated by a conventional formulation method. You can also. In the latter case, in addition to the peptide of the present invention, carriers, excipients and the like that are usually used for drugs can be included as needed without particular limitation. Examples of such carriers are sterilized water, physiological saline, phosphate buffer, culture solution and the like. Furthermore, the pharmaceutical composition of the present invention may contain a stabilizer, a suspension, a preservative, a surfactant and the like, if necessary. The pharmaceutical composition of the present invention can be used for anti-angiogenic purposes.

  In order to induce CTL in vivo, the peptides of the invention can be prepared as a combination composed of two or more of the peptides of the invention. The peptide combination may take the form of a cocktail or may be conjugated to each other using standard techniques. For example, the peptides can be chemically conjugated or expressed as a single fusion polypeptide sequence. The peptides in the combination may be the same or different. By administering the peptides of the present invention, the peptides are presented at high density on the APC by the HLA antigen, and then specifically directed to the complex formed between the presented peptide and the HLA antigen. Reacting CTL is induced. Alternatively, APC (eg, DC) is removed from the subject and then stimulated with the peptides of the invention to obtain APCs that present any of the peptides of the invention on their cell surface. These APCs can be re-administered to a subject to induce CTL in the subject, resulting in increased aggressiveness against vascular endothelial cells that express VEGFR1.

  A pharmaceutical composition for the treatment and / or prevention of diseases mediated by angiogenesis comprising the peptide of the present invention as an active ingredient is also an adjuvant known to efficiently establish cellular immunity. May be included. Alternatively, the pharmaceutical composition of the present invention can be administered together with other active ingredients, or can be administered by formulating into granules. An adjuvant refers to a compound that enhances the immune response to the protein when administered together (or sequentially) with the protein having immunological activity. Adjuvants contemplated herein include those described in the literature (eg, Clin Microbiol Rev 1994, 7: 277-89). Examples of suitable adjuvants include aluminum phosphate, aluminum hydroxide, alum, cholera toxin, salmonella toxin, incomplete Freund's adjuvant (IFA), complete Freund's adjuvant (CFA), ISCOMAtrix, GM-CSF, CpG, oil-in-water type Although emulsion etc. are included, it is not limited to these.

  Furthermore, liposome preparations, granule preparations in which peptides are bound to beads having a diameter of several micrometers, and preparations in which lipids are bound to peptides may be used advantageously.

  In another aspect of the invention, the peptides of the invention may also be administered in the form of a pharmaceutically acceptable salt. Preferred examples of the salt include a salt with an alkali metal, a salt with a metal, a salt with an organic base, a salt with an organic acid, and a salt with an inorganic acid.

In some embodiments, the pharmaceutical composition of the invention may further comprise a component that stimulates CTL. Lipids have been identified as substances that can stimulate CTLs in vivo against viral antigens. For example, palmitic acid residues can be attached to the ε and α amino groups of lysine residues and then linked to the peptides of the invention. The lipidated peptide can then be administered directly in the form of micelles or particles, administered in liposomes, or emulsified in an adjuvant. Another example of lipid stimulation of the CTL response is when E. coli lipoproteins such as tripalmitoyl-S-glycerylcysteinyl-seryl-serine (P3CSS) are used when covalently bound to the appropriate peptide. Can be used to stimulate CTL (eg, Deres et al., Nature
1989, 342: 561-4).

  The method of administration may be oral, intradermal, subcutaneous, intravenous injection, etc., and systemic administration or local administration in the vicinity of the target site. Administration can be by a single dose or can be boosted by multiple doses. The dose of the peptide of the present invention can be appropriately adjusted according to the disease to be treated, the age, body weight, administration method and the like of the patient, and is usually 0.001 mg to 1000 mg, such as 0.001 mg to 1000 mg, such as 0.1 mg to 0.1 mg. 10 mg, which can be administered once every few days to several months. Those skilled in the art can appropriately select an appropriate dose.

(2) Pharmaceutical composition comprising polynucleotide as active ingredient The pharmaceutical composition of the present invention may also comprise a polynucleotide encoding the peptide of the present invention in a form capable of expression. As used herein, the phrase “in expressible form” means that the polynucleotide is expressed in vivo as a polypeptide that, when introduced into a cell, induces an immune response that results in an anti-angiogenic effect. To do. In an exemplary embodiment, the sequence of the polynucleotide of interest includes regulatory elements necessary for expression of the polynucleotide. The polynucleotide can be provided with the necessary ones so that stable insertion into the genome of the target cell is achieved (for a description of homologous recombination cassette vectors, see eg, Thomas KR & Capecchi MR, Cell 1987 , 51: 503-12). See, for example, Wolff et al., Science 1990, 247: 1465-8; US Pat. Nos. 5,580,859; 5,589,466; 5,804,566; 5,739,118; 5,736,524; 5,679,647; and WO98 / 04720 I want to be. Examples of DNA-based delivery technologies include “naked DNA”, facilitated (bupivacaine, polymer, peptide-mediated) delivery, cationic lipid complexes, and particle-mediated (“gene gun”) or pressure-mediated Delivery is included (see, eg, US Pat. No. 5,922,687).

The peptides of the present invention can also be expressed by viral vectors or bacterial vectors. Examples of expression vectors include attenuated viral hosts such as vaccinia virus or fowlpox virus. This approach involves the use of vaccinia virus, for example, as a vector to express nucleotide sequences encoding peptides. When introduced into a host, recombinant vaccinia virus expresses an immunogenic peptide, thereby eliciting an immune response. Vaccinia vectors and methods useful for immunization protocols are described, for example, in US Pat. No. 4,722,848. Another vector is BCG (Bacilli Calmette Guerin). BCG vectors are described in Stover et al., Nature 1991, 351:
456-60. A wide variety of other vectors useful for therapeutic administration or immunization are evident, such as adenovirus and adeno-associated virus vectors, retrovirus vectors, Salmonella typhi vectors, detoxified anthrax toxin vectors, etc. . For example, Shata et al., Mol Med Today 2000, 6: 66-71; Shedlock
et al., J Leukoc Biol 2000, 68: 793-806; Hipp et al., In
See Vivo 2000, 14: 571-85.

  Delivery of the polynucleotide into the patient may be direct, in which case the patient may be directly exposed to a vector carrying the polynucleotide or indirect, in which case first in vitro. The cells are transformed with the polynucleotide of interest and then transplanted into the patient. Each of these two approaches is known as in vivo and ex vivo gene therapy.

For a general review of gene therapy methods, see Goldspiel et al.,
Clinical Pharmacy 1993, 12: 488-505; Wu and Wu,
Biotherapy 1991, 3: 87-95; Tolstoshev, Ann Rev Pharmacol
Toxicol 1993, 33: 573-96; Mulligan, Science 1993, 260:
926-32; Morgan & Anderson, Ann Rev Biochem 1993, 62:
191-217; Trends in Biotechnology 1993, 11 (5): 155-215. Methods generally known in the field of recombinant DNA technology that can also be used in the present invention are described in Ausubel et al., Ed., Current Protocols in Molecular Biology, John Wiley & Sons, NY,
1993; and Krieger, Gene Transfer and Expression, A
Laboratory Manual, Stockton Press, NY, 1990. The administration method may be oral, intradermal, subcutaneous, intravenous injection or the like, and systemic administration or local administration in the vicinity of the target site is used. Administration can be by a single dose or can be boosted by multiple doses. The dosage of the polynucleotide in a suitable carrier, or the dosage of the polynucleotide in a cell transformed with a polynucleotide encoding a peptide of the invention will depend on the disease being treated, the age, weight of the patient, method of administration, etc. It is usually 0.001 mg to 1000 mg, such as 0.001 mg to 1000 mg, such as 0.1 mg to 10 mg, and can be administered once every few days to once every several months. Those skilled in the art can appropriately select an appropriate dose.

X. Methods Using Peptides, Exosomes, APCs, and CTLs The peptides and polynucleotides of the present invention can be used to induce APCs and CTLs. CTLs can also be induced using the exosomes and APCs of the present invention. Peptides, polynucleotides, exosomes, and APCs can be used in combination with the compound as long as any other compound does not inhibit their ability to induce CTL. Therefore, CTL can be induced using any of the aforementioned pharmaceutical compositions of the present invention, and in addition, APC can be induced using those containing the peptide and polynucleotide.

(1) Method for Inducing Antigen Presenting Cell (APC) The present invention provides a method for inducing APC having high CTL inducing ability using the peptide or polynucleotide of the present invention.

The method of the invention comprises contacting APC with a peptide of the invention in vitro, ex vivo or in vivo. For example, a method of contacting APC with the peptide ex vivo may comprise the following steps:
a: recovering APC from the subject; and
b: contacting the APC of step a with the peptide.

  The APC is not limited to a particular type of cell, but is known to present proteinaceous antigens on its cell surface as recognized by lymphocytes, DCs, Langerhans cells, macrophages, B cells, and Contains activated T cells. Since DC has the strongest CTL inducing ability among APCs, DC can be preferably used. Any peptide of the invention can be used alone or with other peptides of the invention.

  On the other hand, when the peptide of the present invention is administered to a subject, APC comes into contact with the peptide in vivo, and as a result, APC having high CTL inducing ability is induced in the body of the subject. Thus, the methods of the invention can include the step of administering to the subject a peptide of the invention. Similarly, when the polynucleotide of the present invention is administered to a subject in an expressible form, the peptide of the present invention is expressed in vivo, which comes into contact with APC in vivo, and as a result, APC having a high CTL inducing ability is produced. Induced in the subject's body. Thus, the present invention can also include the step of administering a polynucleotide of the present invention to a subject. The “expressible form” is described above in the section “IX. Pharmaceutical composition (2) Pharmaceutical composition comprising a polynucleotide as an active ingredient”.

The present invention can also include the step of introducing the polynucleotide of the present invention into APC in order to induce APC having CTL inducing ability. For example, the method may include the following steps:
a: recovering APC from the subject; and
b: introducing a polynucleotide encoding the peptide of the present invention into the APC of step a.
Step b can be performed as described above in section "VI. Antigen-presenting cells".

Accordingly, in one embodiment, the present invention provides a method for inducing APC having CTL inducing ability, comprising the following steps a or b:
a: contacting APC with a peptide of the invention;
b: introducing a polynucleotide encoding the peptide of the present invention into APC.

The above methods can be performed in vitro, ex vivo, or in vivo, but are preferably performed in vitro or ex vivo. The APC used in the above method may be derived from a subject to whom administration of induced APC is scheduled, but may be derived from a different subject. When using APC derived from a subject (donor) that is different from the subject to be administered, the HLA of the subject and the donor must be the same. In the method of the present invention, the HLA of the administration subject and the donor is preferably HLA-A02 (more preferably HLA-A ^* 0201). Alternatively, the APC used in the above method is preferably an APC expressing HLA-A02 (more preferably HLA-A ^* 0201).

  In another embodiment, the present invention also provides a pharmaceutical composition for inducing APC having CTL inducibility, comprising the peptide of the present invention or a polynucleotide encoding the peptide.

  Alternatively, the present invention further provides use of the peptide of the present invention or a polynucleotide encoding the peptide in the manufacture of a pharmaceutical composition for inducing APC having CTL inducing ability.

  Alternatively, the present invention further provides a peptide of the present invention or a polynucleotide encoding the peptide for use in inducing APC having the ability to induce CTL.

  Alternatively, the present invention further relates to a method or process for producing a pharmaceutical composition for inducing APC comprising a peptide of the present invention or a polynucleotide encoding the peptide, pharmaceutically or physiologically. A method or process comprising formulating an acceptable carrier.

  In another embodiment, the present invention also provides a method or process for producing a pharmaceutical composition for inducing APC having CTL inducing ability, comprising the peptide of the present invention or a polynucleotide encoding the peptide. A method or process is provided that comprises admixing with a pharmaceutically or physiologically acceptable carrier.

(2) Method for Inducing CTL The present invention also provides a method for inducing CTL using the peptide, polynucleotide, exosome or APC of the present invention.

  When the peptide, polynucleotide, APC, or exosome of the present invention is administered to a subject, CTL is induced in the subject's body, and the strength of the immune response targeting vascular endothelial cells expressing VEGFR1 is enhanced. Thus, the methods of the invention can include administering to the subject a peptide, polynucleotide, APC, or exosome of the invention.

Alternatively, CTLs can be induced by using them in vitro or ex vivo and then returned to the subject. For example, the method may include the following steps:
a. Recovering APC from the subject,
b. Contacting the APC of step a with a peptide of the invention, and
c. Co-culturing the APC of step b with CD8 positive T cells.

  APC co-cultured with CD8-positive T cells in the above step c may be prepared by introducing a gene containing the polynucleotide of the present invention into APC as described above in the section “VI. Antigen-presenting cells”. it can. However, the present invention is not limited to this, and includes any APC that presents a complex of the HLA antigen and the peptide of the present invention on its surface.

  Instead of such APC, an exosome that presents a complex of the HLA antigen and the peptide of the present invention on its surface can also be used. That is, the present invention can include the step of co-culturing exosomes that present a complex of HLA antigen and the peptide of the present invention on its surface. Such exosomes can be prepared by the methods described above in the section “V. Exosomes”.

  Furthermore, CTL can be induced by introducing a vector containing a polynucleotide encoding each subunit of TCR capable of binding to the peptide of the present invention presented by the HLA antigen on the cell surface into CD8-positive T cells. it can. Such transduction can be performed as described above in the section “VIII. T Cell Receptor (TCR)”.

Accordingly, in one aspect, the present invention provides a method for inducing CTL comprising the step selected from:
a: co-culturing CD8 positive T cells with APC presenting a complex of HLA antigen and the peptide of the present invention on its surface;
b: co-culturing CD8 positive T cells with exosomes presenting a complex of HLA antigen and a peptide of the invention on its surface; and c: the present invention presented by HLA antigen on the cell surface Introducing into a CD8-positive T cell a vector comprising a polynucleotide encoding each subunit of TCR that can bind to the peptide of.

The above methods can be performed in vitro, ex vivo, or in vivo, but are preferably performed in vitro or ex vivo. The APC or exosome and / or CD8 positive T cell used in the above method may be derived from a subject to whom induced CTL administration is scheduled, but is derived from a different subject. Also good. When using APC or exosomes and / or CD8 positive T cells derived from a different subject (donor) than the subject to be administered, the HLA of the subject and the donor needs to be the same. In the method of the present invention, the HLA of the administration subject and the donor is preferably HLA-A02 (more preferably HLA-A ^* 0201). Alternatively, the APC or exosome used in the above method may be an APC or exosome that presents a complex of HLA-A02 (more preferably HLA-A ^* 0201) and the peptide of the present invention on its surface. preferable.

In another aspect, the present invention also provides a pharmaceutical composition for inducing CTL comprising an active ingredient selected from the following:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the invention in an expressible form; and (c) an APC or exosome presenting the peptide of the invention on its surface.

In another aspect, the present invention also provides the use of an active ingredient selected from the following in the manufacture of a pharmaceutical composition for inducing CTL:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the invention in an expressible form; and (c) an APC or exosome presenting the peptide of the invention on its surface.

Alternatively, the present invention further provides an active ingredient selected from among the following for use in the induction of CTL:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the invention in an expressible form; and (c) an APC or exosome presenting the peptide of the invention on its surface.

Alternatively, the present invention further relates to a method or process for producing a pharmaceutical composition for inducing CTL, comprising an active ingredient selected from the following and a pharmaceutically or physiologically acceptable carrier A method or process comprising the step of formulating:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the invention in an expressible form; and (c) an APC or exosome presenting the peptide of the invention on its surface.

In another embodiment, the present invention also provides a method or process for producing a pharmaceutical composition for inducing CTL, wherein the active ingredient selected from the following is pharmaceutically or physiologically acceptable. A method or process comprising the step of mixing with a carrier is provided:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the invention in an expressible form; and (c) an APC or exosome presenting the peptide of the invention on its surface.

XI. Methods for Inducing Immune Responses The present invention further provides methods for inducing immune responses against diseases associated with VEGFR1. Suitable diseases are those mediated by angiogenesis, including various cancers, diseases related to angiogenesis in the choroid (neovascular macular disease: age-related macular degeneration, myopic macular degeneration, retina) Pigmentary striae, central exudative reticulochoroidal disease, various retinal pigment epitheliosis, choroidal atrophy, choroideremia, choroidal osteoma), diabetic retinopathy, rheumatoid arthritis, psoriasis, and atherosclerosis Including, but not limited to.

  The present invention also provides a method of inducing an immune response against vascular endothelial cells that express VEGFR1. In the diseases mediated by angiogenesis as described above, VEGFR1 is found to be strongly expressed in vascular endothelial cells at the disease site. Therefore, when an immune response against vascular endothelial cells expressing VEGFR1 is induced, angiogenesis at the disease site is inhibited as a result. Thus, the present invention also provides a method of inhibiting angiogenesis at a disease site of a disease mediated by angiogenesis.

  The methods of the invention can include administering a composition comprising any of the peptides of the invention or a polynucleotide encoding them. The methods of the present invention also contemplate administration of exosomes or APCs that present any of the peptides of the present invention. For details, please refer to the section “IX. Pharmaceutical composition”, in particular the part describing the use of the pharmaceutical composition of the invention as a vaccine. In addition, exosomes and APCs that can be used in the methods of the invention to induce an immune response include the aforementioned “V. exosomes”, “VI. Antigen presenting cells (APCs)”, and “X. It is described in detail in the sections (1) and (2) of “Method Using Exosome, APC, and CTL”.

In another aspect, the invention also provides a pharmaceutical composition or vaccine for inducing an immune response mediated by angiogenesis and against a disease, comprising an active ingredient selected from: Provide a composition or vaccine:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

Alternatively, the present invention further relates to a pharmaceutical composition or vaccine for inducing an immune response against vascular endothelial cells expressing VEGFR1, which comprises an active ingredient selected from the following: I will provide a:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

Alternatively, the present invention further relates to a pharmaceutical composition or vaccine for inhibiting angiogenesis at a disease site of a disease mediated by angiogenesis, which comprises an active ingredient selected from the following: Provide a composition or vaccine:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

In another aspect, the present invention also provides the use of an active ingredient selected from among the following in the manufacture of a pharmaceutical composition or vaccine for inducing an immune response mediated by angiogenesis and against a disease: :
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

Alternatively, the present invention further provides the use of an active ingredient selected from among the following in the manufacture of a pharmaceutical composition or vaccine for inducing an immune response against vascular endothelial cells expressing VEGFR:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

Alternatively, the present invention further provides the use of an active ingredient selected from among the following in the manufacture of a pharmaceutical composition or vaccine for inhibiting angiogenesis at a disease site of a disease mediated by angiogenesis: :
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; and (d) CTL of the invention.

  The present invention also provides a method or process for producing a pharmaceutical composition that induces an immune response, which may comprise mixing or formulating a peptide of the present invention with a pharmaceutically acceptable carrier. provide.

Alternatively, the method of the invention may comprise administering a vaccine or pharmaceutical composition comprising:
(A) the peptide of the present invention;
(B) a polynucleotide encoding the peptide of the present invention in an expressible form;
(C) APC or exosome presenting the peptide of the invention on its surface; or (d) CTL of the invention.

In the context of the present invention, angiogenesis-mediated diseases associated with VEGFR1 expression can be treated with these active ingredients. Examples of such diseases include various cancers, diseases related to angiogenesis in the choroid (neovascular macular disease: age-related macular degeneration, myopic macular degeneration, retinitis pigmentosa, central exudation Retinopathy of the retina, various retinitis pigmentosa, choroidal atrophy, choroideremia, choroidal osteoma, etc.), diabetic retinopathy, rheumatoid arthritis, psoriasis, and atherosclerosis. Therefore, it is preferable to confirm whether the expression level of VEGFR1 in the subject to be treated is enhanced before administering a vaccine or pharmaceutical composition comprising the active ingredient. Accordingly, in one aspect, the invention provides a method of treating a disease in a patient in need of treatment of a disease that (over) expresses VEGFR1, and such method comprises the following steps:
i) measuring the expression level of VEGFR1 in a biological sample obtained from a subject having a disease to be treated;
ii) comparing the expression level of VEGFR1 with a normal control; and iii) overexpressing VEGFR1 as compared to a normal control with at least one component selected from the group consisting of (a) to (d) above Administering to a subject having a disease.

  Alternatively, the present invention also provides a vaccine or pharmaceutical composition comprising at least one component selected from the group consisting of (a) to (d) above for administration to a subject having. In other words, the present invention further includes a method for identifying a subject to be treated with the peptide of the present invention, the method comprising the step of measuring the expression level of VEGFR1 in a biological sample derived from the subject, wherein the level is the gene. Provides an indication that a subject may have a disease that can be treated with a peptide of the present invention by being elevated relative to a normal control level. The method for treating the disease of the present invention will be described in more detail below.

  According to the present invention, the expression level of VEGFR1 in a biological sample obtained from a subject can be measured.

In one aspect, the invention provides a method of (i) diagnosing whether a subject is suspected of having a disease to be treated, and / or (ii) selecting a subject for treatment of a disease, Such a method includes the following steps:
a) measuring the expression level of VEGFR1 in a biological sample obtained from a subject suspected of having the disease to be treated;
b) comparing the expression level of VEGFR1 to a normal control level;
c) diagnosing the subject as having a disease to be treated when the expression level of VEGFR1 is elevated compared to a normal control level; and
d) selecting the subject for treatment of a disease if the subject is diagnosed in step c) as having a disease to be treated.

Alternatively, such a method may include the following steps:
a) measuring the expression level of VEGFR1 in a biological sample obtained from a subject suspected of having the disease to be treated;
b) comparing the expression level of VEGFR1 to the disease control level;
c) diagnosing the subject as having a disease to be treated if the expression level of VEGFR1 is similar or equivalent compared to the disease control level; and
d) selecting the subject for treatment of a disease if the subject is diagnosed in step c) as having a disease to be treated.

XII. Antibodies The present invention further provides antibodies that bind to the peptides of the present invention. Preferred antibodies specifically bind to peptides of the invention and do not bind (or bind weakly) to non-peptides of the invention. Antibodies against the peptides of the invention can be used in disease diagnostic and prognostic assays, and imaging methodologies.

  The present invention also provides various immunological assays for detecting and / or quantifying the VEGFR1 polypeptide (SEQ ID NO: 155) or fragments thereof, or the peptides or fragments thereof of the present invention. Such assays can optionally include one or more anti-VEGFR1 antibodies that can recognize and bind to the VEGFR1 protein or fragment thereof, or the peptide of the invention or fragment thereof. In the context of the present invention, an anti-VEGFR1 antibody that binds to a VEGFR1 polypeptide preferably recognizes a peptide of the invention. The binding specificity of the antibody can be confirmed by an inhibition test. That is, if the binding between the antibody to be analyzed and the full-length VEGFR1 polypeptide is inhibited in the presence of the peptide of the invention, this indicates that the antibody specifically binds to the peptide of the invention. In the context of the present invention, such immunological assays include various types of radioimmunoassay, immunochromatographic techniques, enzyme-linked immunosorbent assay (ELISA), enzyme-linked immunofluorescence assay (ELIFA). Performed within a variety of immunological assay formats well known in the art, including but not limited to.

  Immunological but non-antibody related assays of the invention can also include T cell immunogenicity assays (inhibitory or stimulatory) and MHC binding assays. In addition, the present invention contemplates immunological imaging methods that can detect diseases that express VEGFR1, examples of which include radioscintigraphic imaging methods that use the labeled antibodies of the present invention, It is not limited to this. Such assays are used clinically in the detection, monitoring, and prognosis of diseases that express VEGFR1, and examples of such diseases include various cancers, diseases associated with angiogenesis in the choroid (neoplasia) Vascular macular degeneration: age-related macular degeneration, myopic macular degeneration, retinitis pigmentosa, central exudative retinochoroidosis, various retinal pigment epitheliopathy, choroidal atrophy, colloideremia, choroidal osteoma) These include, but are not limited to diabetic retinopathy, rheumatoid arthritis, psoriasis, and atherosclerosis.

  The antibody of the present invention can be used in any form such as a monoclonal antibody or a polyclonal antibody, for example, antiserum obtained by immunizing animals such as rabbits with the peptide of the present invention, all classes of polyclonal antibodies and monoclonal antibodies. It may further include antibodies, human antibodies, and humanized antibodies produced by genetic recombination.

  The VEGFR1 polypeptide or fragment thereof used as an antigen for obtaining an antibody, or the peptide or fragment thereof of the present invention can be produced by chemical synthesis or genetic engineering based on the nucleotide sequence or amino acid sequence disclosed herein. It can be obtained by a technique.

  According to the present invention, a peptide used as an immunizing antigen may be a complete protein or a partial peptide of the protein. The partial peptide can comprise, for example, a VEGFR1 polypeptide or an amino (N) terminal fragment or a carboxy (C) terminal fragment of a peptide of the invention.

  As used herein, an antibody of the invention is defined as a protein that reacts with either the full length or a fragment of the VEGFR1 peptide. In a preferred embodiment, the antibody of the present invention can recognize the peptide of the present invention. Methods for synthesizing oligopeptides are well known in the art. After synthesis, the peptide may optionally be purified before use as an immunogen. In the context of the present invention, oligopeptides (eg 9 mer or 10 mer) may be bound or linked to a carrier in order to increase immunogenicity. As a carrier, keyhole limpet hemocyanin (KLH) is well known. Methods for conjugating KLH and peptides are also well known in the art.

  Alternatively, a gene encoding a peptide of the invention or a fragment thereof can be inserted into a known expression vector, which is then used to transform host cells as described herein. The desired peptide or fragment thereof can be recovered from the exterior or interior of the host cell by any standard method and can later be used as an antigen. Alternatively, whole cells expressing a peptide or a lysate thereof, or a chemically synthesized peptide may be used as an antigen.

  Although any mammal can be immunized with the antigen, it is preferred to take into account compatibility with the parental cell used for cell fusion. In general, Rodentia, Lagomorpha, or Primate animals can be used. Rodent animals include, for example, mice, rats, and hamsters. Rabbits include, for example, rabbits. Primatological animals include, for example, monkeys from the Macaca fascicularis, rhesus monkeys, baboons, and chimpanzees (Catarrhini) (old world monkeys).

  Methods for immunizing animals with antigens are known in the art. Intraperitoneal or subcutaneous injection of antigen is a standard method for immunizing mammals. More specifically, the antigen is diluted with an appropriate amount of phosphate buffered saline (PBS), physiological saline or the like and suspended. If desired, the antigen suspension can be mixed with an appropriate amount of a standard adjuvant, such as Freund's complete adjuvant, emulsified and administered to a mammal. Thereafter, the antigen mixed with an appropriate amount of Freund's incomplete adjuvant is preferably administered several times every 4 to 21 days. A suitable carrier may be used for immunization. After immunization as described above, serum can be examined by standard methods for increasing amounts of the desired antibody.

  Polyclonal antibodies against the peptides of the present invention can be prepared by recovering blood from the immunized mammal examined for an increase in the desired antibody in the serum and separating the serum from the blood by any conventional method. . Polyclonal antibodies may include serum containing polyclonal antibodies, and fractions containing polyclonal antibodies may be isolated from the serum. Immunoglobulin G or M is obtained from a fraction that recognizes only the peptide of the present invention by using, for example, an affinity column to which the peptide of the present invention is bound, and further using this protein A or protein G column. It can be purified and prepared.

  In order to prepare a monoclonal antibody, immune cells are collected from a mammal immunized with an antigen, confirmed for an increase in the level of a desired antibody in serum as described above, and subjected to cell fusion. The immune cells used for cell fusion can be preferably obtained from the spleen. Other preferred parental cells to be fused with the above immune cells include, for example, mammalian myeloma cells, and more preferably myeloma cells that have acquired properties for selection of fusion cells with drugs.

  According to a known method, for example, the method of Milstein et al. (Galfre and Milstein, Methods Enzymol 73: 3-46 (1981)), the above immune cells and myeloma cells can be fused.

  The resulting hybridomas from cell fusion can be selected by culturing them in a standard selective medium such as HAT medium (medium containing hypoxanthine, aminopterin, and thymidine). Cell culture typically continues in HAT medium for days to weeks, a period sufficient for all other cells (non-fused cells) except the desired hybridoma to die. Thereafter, standard limiting dilution can be performed to screen and clone hybridoma cells producing the desired antibody.

  In addition to the above methods of immunizing non-human animals with antigens to prepare hybridomas, human lymphocytes such as lymphocytes infected with EB virus can be transformed with peptides, cells expressing the peptides, or lysates thereof. It is also possible to immunize in vitro. Subsequently, the lymphocyte after immunization is fused with an infinitely-dividable human-derived myeloma cell such as U266 to obtain a hybridoma that produces a desired human antibody that can bind to the peptide (Japanese Patent Application Laid-Open No. Sho A). 63-17688).

  Subsequently, the obtained hybridoma is transplanted into the abdominal cavity of the mouse, and ascites is extracted. The obtained monoclonal antibody can be purified by, for example, ammonium sulfate precipitation, protein A or protein G column, DEAE ion exchange chromatography, or an affinity column to which the peptide of the present invention is bound. The antibodies of the present invention can be used not only for purification and detection of the peptides of the present invention but also as candidates for agonists and antagonists of the peptides of the present invention.

  Alternatively, immune cells that produce antibodies, such as immunized lymphocytes, can be immortalized by oncogenes and used to prepare monoclonal antibodies.

The monoclonal antibodies thus obtained can also be prepared recombinantly using genetic engineering techniques (eg Borrebaeck, published in the UK by MacMillan Publishers LTD (1990)).
and Larrick, Therapeutic Monoclonal Antibodies). For example, DNA encoding an antibody is cloned from an immune cell such as an antibody-producing hybridoma or immunized lymphocyte, inserted into an appropriate vector, and then introduced into a host cell to prepare a recombinant antibody. Can do. The present invention also provides a recombinant antibody prepared as described above.

Furthermore, the antibody of the present invention may be an antibody fragment or a modified antibody as long as it binds to one or more of the peptides of the present invention. For example, an antibody fragment may be Fab, F (ab ′) ₂ , Fv, or a single chain Fv (scFv) in which Fv fragments from H and L chains are linked by a suitable linker (Huston
et al., Proc Natl Acad Sci USA 85: 5879-83 (1988)). More specifically, an antibody fragment can be prepared by treating an antibody with an enzyme such as papain or pepsin. Alternatively, a gene encoding the antibody fragment can be constructed, inserted into an expression vector, and expressed in a suitable host cell (eg, Co et al., J Immunol 152: 2968-76 (1994); Better
and Horwitz, Methods Enzymol 178: 476-96 (1989); Pluckthun
and Skerra, Methods Enzymol 178: 497-515 (1989); Lamoyi,
Methods Enzymol 121: 652-63 (1986); Rousseaux et al.,
Methods Enzymol 121: 663-9 (1986); Bird and Walker,
Trends Biotechnol 9: 132-7 (1991)).

  Antibodies can be modified by conjugation with various molecules such as polyethylene glycol (PEG). The present invention provides such modified antibodies. Modified antibodies can be obtained by chemically modifying antibodies. These modification methods are routine in the art.

  Alternatively, the antibody of the present invention is a chimeric antibody between a variable region derived from a non-human antibody and a constant region derived from a human antibody, or a complementarity determining region (CDR) derived from a non-human antibody and a human antibody. It can also be obtained as a humanized antibody comprising a framework region (FR) derived from and a constant region. Such antibodies can be prepared according to known techniques. Humanization can be performed by replacing the corresponding sequence of a human antibody with a rodent CDR or CDR sequence (see, eg, Verhoeyen et al., Science 239: 1534-1536 (1988)). . Accordingly, such humanized antibodies are chimeric antibodies in which substantially less than a human variable domain has been replaced by the corresponding sequence from a non-human species.

  In addition to human framework and constant regions, fully human antibodies that also contain human variable regions can be used. Such antibodies can be generated using various techniques known in the art. For example, in vitro methods include the use of recombinant libraries of human antibody fragments displayed on bacteriophages (eg, Hoogenboom & Winter, J. Mol. Biol. 227: 381 (1991)). Similarly, human antibodies can be made by introducing human immunoglobulin loci into transgenic animals, such as mice, in which the endogenous immunoglobulin genes are partially or completely inactivated. This approach is described, for example, in US Pat. Nos. 6,150,584, 5,545,807; 5,545,806; 5,569,825; 5,625,126; 5,633,425;

The antibody obtained as described above may be purified to homogeneity. For example, separation and purification of antibodies can be performed according to separation and purification methods used for general proteins. For example, but not limited to, appropriately selecting and combining the use of column chromatography such as affinity chromatography, filters, ultrafiltration, salting out, dialysis, SDS polyacrylamide gel electrophoresis, and isoelectric focusing Antibodies can be separated and isolated (Antibodies: A Laboratory Manual. Ed Harlow and David Lane, Cold
Spring Harbor Laboratory (1988)). Protein A and protein G columns can be used as affinity columns. Exemplary protein A columns to be used include, for example, Hyper D, POROS, and Sepharose F.M. F. (Pharmacia) is included.

Exemplary chromatography includes, in addition to affinity chromatography, for example, ion exchange chromatography, hydrophobic chromatography, gel filtration, reverse phase chromatography, adsorption chromatography, etc. (Strategies for Protein Purification and Characterization: A
Laboratory Course Manual. Ed Daniel R. Marshak et al., Cold Spring
Harbor Laboratory Press
(1996)). Chromatographic procedures can be performed by liquid phase chromatography such as HPLC and FPLC.

  For example, the antigen-binding activity of the antibody of the present invention using absorbance measurement, enzyme-linked immunosorbent assay (ELISA), enzyme-linked immunosorbent assay (EIA), radioimmunoassay (RIA), and / or immunofluorescence. Can be measured. In the case of ELISA, the antibody of the present invention is immobilized on a plate, the peptide of the present invention is added to the plate, and then a sample containing a desired antibody such as a culture supernatant of antibody-producing cells or a purified antibody is added. A secondary antibody that recognizes the primary antibody and is labeled with an enzyme such as alkaline phosphatase is then added and the plate is incubated. Subsequently, after washing, an enzyme substrate such as p-nitrophenyl phosphate is added to the plate, the absorbance is measured, and the antigen binding activity of the sample is evaluated. In order to evaluate the binding activity of an antibody, a peptide fragment such as a C-terminal or N-terminal fragment may be used as an antigen. In order to evaluate the activity of the antibody of the present invention, BIAcore (Pharmacia) may be used.

  By exposing the antibody of the present invention to a sample considered to contain the peptide of the present invention, and detecting or measuring an immune complex formed by the antibody and the peptide, the peptide of the present invention can be obtained by the above method. Can be detected or measured. Since the method for detecting or measuring a peptide according to the present invention can specifically detect or measure a peptide, this method can be used in various experiments using the peptide.

XIII. Vectors and host cells The present invention also provides vectors and host cells into which nucleotides encoding the peptides of the present invention have been introduced. The vectors of the invention can be used to retain the nucleotides of the invention, in particular DNA, in host cells, to express the peptides of the invention, or to administer the nucleotides of the invention for gene therapy.

When E. coli is the host cell and the vector is amplified in large quantities by amplification in E. coli (eg, JM109, DH5α, HB101, or XL1Blue), the vector is a “replication origin” for amplification in E. coli, It is necessary to have a marker gene (for example, a drug resistance gene selected by a drug such as ampicillin, tetracycline, kanamycin, chloramphenicol) for selecting the transformed E. coli. For example, M13 vectors, pUC vectors, pBR322, pBluescript, pCR-Script and the like can be used. In addition, pGEM-T, pDIRECT, and pT7 can also be used for cDNA subcloning and extraction, similar to the vectors described above. When the vector is used for production of the protein of the present invention, an expression vector can be used. For example, an expression vector to be expressed in E. coli must have the above characteristics in order to amplify in E. coli. When E. coli such as JM109, DH5α, HB101, or XL1 Blue is used as the host cell, the vector can be a promoter that can efficiently express the desired gene in E. coli, such as the lacZ promoter (Ward et al., Nature 341: 544-6
(1989); FASEB J 6: 2422-7 (1989)), araB promoter (Better et al., Science 240: 1041-3
(1988)), it is necessary to have a T7 promoter and the like. In this regard, for example, pGEX-5X-1 (Pharmacia), “QIAexpress system” (Qiagen), pEGFP, and pET (where the host is preferably BL21 expressing T7 RNA polymerase) of the above vector. Can be used instead. Furthermore, the vector may contain a signal sequence for peptide secretion. An exemplary signal sequence that causes the peptide to be secreted into the periplasm of E. coli is the pelB signal sequence (Lei et al., J Bacteriol 169: 4379
(1987)). Means for introducing the vector into the target host cell include, for example, the calcium chloride method and the electroporation method.

  In addition to E. coli, for example, expression vectors derived from mammals (eg, pcDNA3 (Invitrogen), and pEGF-BOS (Nucleic Acids Res 18 (17): 5322 (1990)), pEF, pCDM8), expression from insect cells Vectors (eg, “Bac-to-BAC baculovirus expression system” (GIBCO BRL), pBacPAK8), plant-derived expression vectors (eg, pMH1, pMH2), animal virus-derived expression vectors (eg, pHSV, pMV, pAdexLcw) ), Retrovirus-derived expression vectors (eg, pZIpneo), yeast-derived expression vectors (eg, “Pichia expression kit” (Invitrogen), pNV11, SP-Q01), and Bacillus subtilis Expression vectors (eg, pPL608, pKTH50) can be used for production of the polypeptides of the invention.

In order for a vector to be expressed in animal cells such as CHO, COS, or NIH3T3 cells, the vector must be a promoter required for expression in such cells, such as the SV40 promoter (Mulligan et al., Nature 277: 108
(1979)), MMLV-LTR promoter, EF1α promoter (Mizushima et al., Nucleic Acids Res 18: 5322 (1990)), CMV promoter and the like, and preferably a marker gene for selecting a transformant (eg, drug (For example, a drug resistance gene selected by neomycin, G418). Examples of known vectors having these characteristics include, for example, pMAM, pDR2, pBK-RSV, pBK-CMV, pOPRSV, and pOP13.

  Although the present invention has been described in detail herein with reference to specific embodiments thereof, the foregoing description is illustrative and explanatory in nature and is intended to describe the invention and preferred embodiments thereof. It should be understood that Those skilled in the art will readily appreciate through routine experimentation that various changes and modifications can be made therein without departing from the spirit and scope of the invention. Accordingly, the invention is intended to be defined not by the above description, but by the following claims and their equivalents.

Candidate selection of peptides derived from VEGFR1
The 9mer and 10mer peptides derived from VEGFR1 that bind to the HLA-A ^* 0201 molecule are linked to the binding prediction software “BIMAS” (www.bimas.cit.nih.gov/molbio/hla_bind) (Parker
et al. (J Immunol 1994, 152 (1): 163-75), Kuzushima et al. (Blood 2001, 98 (6): 1872-81)) and “NetMHC” (www.cbs.dtu.dk/services / NetMHC /)
(Buus et al., Tissue Antigens. 2003 Nov, 62 (5): 378-84; Nielsen et al., Protein
Sci. 2003 May, 12 (5): 1007-17, Bioinformatics. 2004 Jun 12:20 (9): 1388-97).

  Tables 1 and 2 show the HLA-A02 binding 9mer and 10mer peptides of VEGFR1 in descending order of binding affinity. A total of 153 peptides with potential HLA-A02 binding ability were selected.

開始位置は、VEGFR1のＮ末端からのアミノ酸残基の数を示す。 (Table 1-1) HLA-A02-binding 9mer peptide derived from VEGFR1

The starting position indicates the number of amino acid residues from the N-terminus of VEGFR1.

開始位置は、VEGFR1のＮ末端からのアミノ酸残基の数を示す。 (Table 1-2) HLA-A02-binding 9mer peptide derived from VEGFR1

The starting position indicates the number of amino acid residues from the N-terminus of VEGFR1.

開始位置は、VEGFR1のＮ末端からのアミノ酸残基の数を示す。 (Table 2-1) HLA-A02 binding 10mer peptide derived from VEGFR1

The starting position indicates the number of amino acid residues from the N-terminus of VEGFR1.

開始位置は、VEGFR1のＮ末端からのアミノ酸残基の数を示す。 (Table 2-2) HLA-A02 binding 10mer peptide derived from VEGFR1

The starting position indicates the number of amino acid residues from the N-terminus of VEGFR1.

Peptide Synthesis These peptides can be synthesized according to standard solid phase synthesis methods and purified by reverse phase high performance liquid chromatography (HPLC). The purity (> 90%) and identity of the peptides can be measured by analytical HPLC and mass spectrometry, respectively. The peptide can be dissolved in dimethyl sulfoxide (DMSO) at 20 mg / ml and stored at -80 ° C.

Using in vitro CTL-derived monocyte-derived dendritic cells (DCs) as antigen-presenting cells (APCs), cytotoxic T lymphocyte (CTL) responses to peptides presented on human leukocyte antigen (HLA) Induce. DCs are generated in vitro as described elsewhere (Nakahara S et al., Cancer Res
2003 Jul 15, 63 (14): 4112-8). Specifically, peripheral blood mononuclear cells (PBMC) isolated from healthy volunteers (HLA-A ^* 0201 positive) with Ficoll-Plaque (Pharmacia) solution are attached to plastic tissue culture dishes (Becton Dickinson) And concentrate them as monocyte fractions. 1000 U / ml granulocyte macrophage colony stimulating factor (GM-CSF) (R & D System) and 1000 U / ml interleukin in AIM-V medium (Invitrogen) containing 2% heat-inactivated autoserum (AS) A population enriched for monocytes is cultured in the presence of (IL) -4 (R & D System). After 7 days of culture, cytokine-induced DCs are pulsed with 20 μg / ml of each synthetic peptide in AIM-V medium at 37 ° C. for 3 hours in the presence of 3 μg / ml β2-microglobulin. The generated cells express DC related molecules such as CD80, CD83, CD86, and HLA class II on their cell surface. These peptide-pulsed DCs are then inactivated by X-ray irradiation (20 Gy) and mixed with autologous CD8-positive T cells obtained by positive selection using CD8 positive Isolation Kit (Dynal) at a ratio of 1:20. . These cultures were prepared in 48-well plates (Corning), each well containing 3 × 10 ⁵ DCs pulsed with 1.5 × 10 ⁴ peptide pulses in 0.5 ml AIM-V / 2% AS medium. Of CD8 + T cells and 10 ng / ml IL-7 (R & D System). After 3 days, IL-2 (CHIRON) is added to these cultures to a final concentration of 20 IU / ml. On day 7 and 14, T cells are further stimulated with peptide-pulsed autologous DCs. The DC is prepared each time by the same method as above. On day 21, after the third peptide stimulation, CTL are tested against peptide-pulsed TISI cells or T2 cells (Tanaka H et al., Br J Cancer 2001 Jan 5, 84 (1): 94-9; Umano Y et al., Br J Cancer 2001 Apr 20, 84 (8): 1052-7; Uchida N et al., Clin Cancer Res 2004 Dec 15, 10 (24): 8577-86; Suda T et al., Cancer Sci 2006 May, 97 (5): 411-9; Watanabe T et al., Cancer Sci 2005 Aug, 96 (8): 498-506). Peptide-specific CTL activity is determined by an interferon (IFN) -γ enzyme-linked immunospot (ELISPOT) assay.

CTL proliferation
Riddell et al. (Walter EA et al., N
Engl J Med 1995 Oct 19, 333 (16): 1038-44; Riddell SR et
al., Nat Med 1996 Feb, 2 (2): 216-23), using a method similar to that described in the above IELISPOT assay, CTL in which peptide-specific CTL activity was confirmed in culture. Proliferate. In the presence of 40 ng / ml anti-CD3 monoclonal antibody (Pharmingen), together with two human B lymphoblastoid cell lines inactivated by mitomycin C, a total of 5 × 10 ⁴ CTLs in 25 ml AIM-V / Suspend in 5% AS medium. One day after the start of culture, 120 IU / ml IL-2 is added to the culture. On days 5, 8, and 11, fresh AIM-V / 5% AS medium containing 30 IU / ml IL-2 is fed to the culture (Tanaka H et al., Br J Cancer 2001 Jan 5 , 84 (1): 94-9; Umano Y et al., Br J Cancer 2001 Apr 20, 84 (8): 1052-7; Uchida N et al., Clin Cancer Res 2004 Dec 15, 10 (24): 8577-86; Suda T et al., Cancer Sci 2006 May, 97 (5): 411-9; Watanabe T et al., Cancer Sci 2005 Aug, 96 (8): 498-506). The peptide-specific CTL activity of the CTL line grown as described above is measured by IFN-γ ELISA assay.

Establishment of a CTL clone A CTL clone is established from a CTL in which peptide-specific CTL activity has been confirmed as described above. Dilute to 0.3, 1, and 3 / well CTL in 96 round bottom microtiter plates (Nalge Nunc International). CTL was combined with 2 human B lymphoblastoid cell lines at 1 × 10 ⁴ cells / well, 30 ng / ml anti-CD3 antibody, and 125 U / ml IL-2 for a total of 150 μl / well of 5% AS Culture in AIM-V medium. After 10 days, 50 μl / well of IL-2 is added to the medium so that the final concentration of IL-2 reaches 125 U / ml. On day 14, CTL activity was tested, and CTL clones with confirmed peptide-specific CTL activity were propagated using the same method as above (Uchida N et al., Clin Cancer Res 2004 Dec 15, 10 (24) : 8577-86; Suda T et al., Cancer Sci 2006 May, 97 (5): 411-9; Watanabe T et al., Cancer Sci 2005 Aug, 96 (8): 498-506). The peptide-specific CTL activity of established CTL clones is measured by IFN-γ enzyme-linked immunosorbent assay (ELISA) for IFN-γ production from CTL clones against peptide-pulsed target cells.

Specific CTL activity against target cells expressing VEGFR1 and HLA-A * 0201
Adjustment of target cells expressing VEGFR1 and HLA-A * 0201 can be performed as follows. A cDNA encoding the VEGFR1 gene and the open reading frame of HLA-A ^* 0201 is amplified by PCR. The PCR amplification product is cloned into the pCAGGS vector. The plasmid is transfected into COS7, a negative cell line for the VEGFR1 gene and HLA-A02, using Lipofectamine 2000 (Invitrogen) according to the manufacturer's recommended procedure. Two days after transfection, transfected cells are harvested using Invitrogen and used as target cells (5 × 10 ⁴ cells / well) for CTL activity assay.

  Using the CTL clone established as described above as an effector cell, the specific CTL activity against the target cell is measured. As a control for the target cells, COS7 cells transfected with either the VEGFR1 gene or HLA-A * 0201 can be used.

Homology analysis of antigenic peptides As mentioned above, the immunogenicity of peptides that could induce CTLs with peptide-specific CTL activity is derived from other molecules known to sensitize the human immune system May be due to the fact that it is homologous. To negate this possibility, homology analysis is performed on these peptide sequences as queries using the BLAST algorithm (www.ncbi.nlm.nih.gov/blast/blast.cgi).

INDUSTRIAL APPLICABILITY The present invention is capable of inducing a strong and specific immune response against vascular endothelial cells at a disease site with abnormal angiogenesis, and a wide variety of diseases mediated by angiogenesis. A novel peptide derived from VEGFR1 is provided. Such peptides may be useful as peptide vaccines against diseases mediated by angiogenesis associated with VEGFR1, and examples of such diseases include various cancers, diseases associated with angiogenesis in the choroid (neovascular Macular dysfunction: age-related macular degeneration, myopic macular degeneration, retinitis pigmentosa, central exudative retina choroidopathy, various retinal pigment epitheliopathy, choroidal atrophy, choroideremia, choroidal osteoma, etc.), diabetes Include, but are not limited to, retinopathy, rheumatoid arthritis, psoriasis, and atherosclerosis.

Claims (18)

An isolated peptide having the ability to induce CTL, comprising an amino acid sequence selected from the following group:
(A) an amino acid sequence selected from the group consisting of SEQ ID NO: 1 to 153; and (b) one, two, or several amino acid sequences selected from the group consisting of SEQ ID NO: 1 to 153 An amino acid sequence in which amino acids are substituted, deleted, inserted and / or added.   2. The isolated peptide of claim 1, which is a nonapeptide or a decapeptide. 3. An isolated peptide according to claim 1 or 2 having one or both of the following characteristics:
(A) the second amino acid from the N-terminus is an amino acid selected from the group consisting of leucine and methionine, or has been modified to be the amino acid, and (b) the C-terminal amino acid is valine And an amino acid selected from the group consisting of leucine or modified to be said amino acid.   An isolated polynucleotide encoding the isolated peptide of any one of claims 1-3.   A composition for inducing CTL, comprising one or more peptides according to any one of claims 1 to 3, or one or more polynucleotides according to claim 4. object.   A pharmaceutical composition for the treatment and / or prevention of diseases mediated by angiogenesis and / or prevention of its recurrence after surgery, comprising one or more of the claims 1 to 3 A pharmaceutical composition comprising a plurality of types of peptides or one or more types of polynucleotides according to claim 5.   A pharmaceutical composition for inhibiting angiogenesis at a disease site of a disease mediated by angiogenesis, the one or more peptides according to any one of claims 1 to 3, or claim 6. A pharmaceutical composition comprising one or more polynucleotides according to 5.   The disease mediated by angiogenesis is cancer, a disease associated with angiogenesis in the choroid (neovascular macular disease), diabetic retinopathy, rheumatoid arthritis, psoriasis, and atherosclerosis, or 8. The pharmaceutical composition according to 7.   Diseases related to angiogenesis in the choroid include age-related macular degeneration, myopic macular degeneration, retinitis pigmentosa, central exudative reticulochoroidosis, various retinal pigment epitheliopathy, choroidal atrophy, colloidemia, The pharmaceutical composition according to claim 8, which is choroidal osteoma.   The pharmaceutical composition according to claim 8, which is used for suppressing cancer growth or metastasis.   11. The pharmaceutical composition according to any one of claims 6 to 10, which is formulated for administration to a subject whose HLA antigen is HLA-A02. A method for inducing antigen-presenting cells (APC) having CTL inducing ability, comprising a step selected from the group consisting of
(A) contacting APC with the peptide according to any one of claims 1 to 3 in vitro, ex vivo or in vivo; and (b) encoding the peptide according to any one of claims 1 to 3. Introducing a polynucleotide to APC. A method of inducing CTL comprising one stage selected from the group consisting of:
(A) co-culturing CD8 positive T cells with APC presenting a complex of the HLA antigen and the peptide according to any one of claims 1 to 3 on its surface;
(B) co-culturing a CD8 positive T cell with an exosome presenting a complex of HLA antigen and the peptide of any one of claims 1 to 3 on its surface; and (c) a cell surface A vector comprising a polynucleotide encoding a T cell receptor (TCR) subunit capable of binding to the peptide according to any one of claims 1 to 3 presented above by an HLA antigen is introduced into a CD8-positive T cell. Stage to do.   An isolated APC that presents a complex of an HLA antigen and the peptide of any one of claims 1 to 3 on its surface.   15. The APC of claim 14, wherein the APC is derived by the method of claim 12.   An isolated CTL targeting the peptide of any one of claims 1-3.   The CTL of claim 16, wherein the CTL is derived by the method of claim 13.   4. By angiogenesis in a subject comprising administering to the subject a composition comprising the peptide of any one of claims 1-3, an immunologically active fragment thereof, or a polynucleotide encoding the peptide or the fragment. A method of inducing an immune response against a mediated disease.