ES2494921T3 - Anticuerpo que sustituye la función del factor VIII de coagulación sanguínea - Google Patents
Anticuerpo que sustituye la función del factor VIII de coagulación sanguínea Download PDFInfo
- Publication number
- ES2494921T3 ES2494921T3 ES06730769.4T ES06730769T ES2494921T3 ES 2494921 T3 ES2494921 T3 ES 2494921T3 ES 06730769 T ES06730769 T ES 06730769T ES 2494921 T3 ES2494921 T3 ES 2494921T3
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- Prior art keywords
- coagulation factor
- a44fr
- pcagg
- a44lr3
- a44lf3
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/36—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against blood coagulation factors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/40—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against enzymes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/46—Hybrid immunoglobulins
- C07K16/468—Immunoglobulins having two or more different antigen binding sites, e.g. multifunctional antibodies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/31—Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
- C07K2317/622—Single chain antibody (scFv)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/75—Agonist effect on antigen
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- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
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- Biochemistry (AREA)
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- General Chemical & Material Sciences (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Un anticuerpo biespecífico que puede sustituir funcionalmente al factor VIII de coagulación y que presenta la actividad para mejorar la activación del factor X, que comprende: un primer dominio que reconoce al factor de coagulación IX y/o al factor de coagulación IX activado; y un segundo dominio que reconoce al factor de coagulación X, donde el primer dominio comprende un primer polipéptido que comprende la cadena H de un anticuerpo contra el factor de coagulación IX y/o el factor de coagulación IX activado; el segundo dominio comprende un segundo polipéptido que comprende la cadena H de un anticuerpo contra el factor de coagulación X; y tanto el primero como el segundo dominio comprenden un tercer polipéptido que comprende una cadena L compartida en común de un anticuerpo contra el factor de coagulación IX, el factor de coagulación IX activado o el factor de coagulación X, donde el tercer polipéptido comprende un sitio de unión a antígenos que comprende las CDR1, 2 y 3 seleccionadas individualmente de CDR1, 2 y 3 de cada cadena L de dos o más anticuerpos;
Description
E06730769
22-08-2014
GAAGCGATCAGGGACTCCACTGTACCGGTAGGATGCCGAGTAAATCAGTAGTTTAGG B26LF4_A44fr (SEQ ID NO: 61) CTGGCAGATTATCTCTGTCAGCAATATAACAGCTATCCACTCACGTTCGGTGGTGGGA CC A69LR1_A44fr (SEQ ID NO: 62)
5 GGCTACAGCAGTACTCACATCCTGACTGGCCTTGCAGGTGATGCTGACCCTGTCTCCT ACTGATGTGGA A5OLF4_A44fr (SEQ ID NO: 63) CTGGCAGATTATCTCTGTCAGCAATATAGCAGCTATTTAACGTTCGGTGGTGGGACC scback (SEQ ID NO: 64) TTACTCGCGGCCCAGCCGGCCATGGCGGACTACAAAG
10 scfor (SEQ ID NO: 65) GGAATTCGGCCCCCGAG Se mezcló 1 µL de cada oligo ADN sintetizado preparado a 10 µM en la combinación que se muestra en la tabla 1, y
se prepararon 45 µL de las soluciones de reacción que comprenden 1x de tampón agregado de enzimas, 0,33 mM de dNTPs, 2,5 unidades de Proof Start Polymerase (Qiagen) o LATaq (TAKARA). Después de calentar a 94°C
15 durante 5 minutos, se llevaron a cabo 7 ciclos de reacciones a 94°C durante un minuto y 63 °C durante 4 minutos, posteriormente se agregaron 5 µL cada solución de 5 µM de scback y 5 µM de scfor, y se llevaron a cabo 30 ciclos de reacciones a 94°C durante 30 segundos, 55°C durante 30 segundos, y 72°C durante 30 segundos para amplificar el gen VL.
- BBA :
- B26LR1_A44fr B26LR2_A44fr A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- BAA :
- B26LR1_A44fr A44LR2 A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- ABA :
- A44LR1 B26LR2_A44fr A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- AAA :
- A44LR1 A44LR2 A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- AAa :
- A44LR1 A44LR2 A50LF4_A44fr A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- BAa :
- B26LR1_A44fr A44LR2 A50LF4_A44fr A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- ABa :
- A44LR1 B26LR2_A44fr A50LF4_A44fr A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- BBa :
- B26LR1_A44fr B26LR2_A44fr A50LF4_A44fr A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- aAA :
- A69LR1_A44fr A44LR2 A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- aBA :
- A69LR1_A44fr B26LR2_A44fr A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4
- BBA(G) :
- B26LR1_A44fr B26LR2_A44fr A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- BAA(G) :
- B26LR1_A44fr A44LR2 A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- ABA(G) :
- A44LR1 B26LR2_A44fr A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- AAA(G) :
- A44LR1 A44LR2 A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- AAa(G) :
- A44LR1 A44LR2 A50LF4_A44fr A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- Baa(G) :
- B26LR1_A44fr A44LR2 A50LF4_A44fr A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- ABa(G) :
- A44LR1 B26LR2_A44fr A50LF4_A44fr A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- BBa(G) :
- B26LR1_A44fr B26LR2_A44fr A50LF4_A44fr A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- aAA(G) :
- A69LR1_A44fr A44LR2 A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
- aBA(G) :
- A69LR1_A44fr B26LR2_A44fr A44LF4 A44LF1 A44LF2 A44LF3 A44LR3 A44LR4Gly
32
E06730769
22-08-2014
Después de la realización de la PCR, los productos se purificaron a partir de todas las soluciones de la reacción mediante el uso del kit de purificación de PCR QIAquick (Qiagen) a través del procedimiento descrito en el manual de instrucciones adjunto, y se eluyeron mediante el uso de agua esterilizada. Después de que se digirieron los fragmentos con la enzima de restricción Sfi I (TOYOBO), se sometieron a electroforesis en gel de agarosa al 2%. 5 Los fragmentos de amplificación que tienen aproximadamente 0,4 kb se purificaron mediante el uso del kit de extracción en gel QIAquick (QIAGEN) a través del procedimiento descrito en el manual de instrucciones adjunto y se eluyeron mediante el uso de agua esterilizada. Los fragmentos obtenidos se ligaron mediante el uso de alta ligación (TOYOBO) con el vector de expresión de cadena L descrito anteriormente pCAGG-κ que se había digerido con Sfi I. Se utilizó parte de cada solución de reacción para transformar la cepa DH5 α E. coli (TOYOBO). Se determinaron las 10 secuencias de nucleótidos y se confirmaron mediante el uso del kit de secuenciación BigDye Terminator Cycle (Applied Biosystems) con el secuenciador de ADN ABI PRISM 3700 DNA Sequencer (Applied Biosystems) de conformidad con el procedimiento descrito en el manual de instrucciones adjunto. pCAGG-A44BBA se obtuvo mediante inserción del fragmento BBA y otros vectores de expresión se obtuvieron de forma similar mediante inserción de otros fragmentos VL. Las secuencias de región variable de anticuerpos correspondientes se describen 15 en las siguientes SEQ ID NO. Tabla 2
- SEQ ID NO de nucleótidos:
- SEQ ID NO de aminoácidos:
- (1) AAA
- (pAGG-A44L) 66 67
- (2) BBA
- (pCAGG-A44BBA) 68 69
- (3) BAA
- (pCAGG-A44BAA) 70 71
- (4) ABA
- (pCAGG-A44ABA) 72 73
- (5) AAa
- (pCAGG-A44AAa) 74 75
- (6) BAa
- (pCAGG-A44BAa) 76 77
- (7) ABa
- (pCAGG-A44ABa) 78 79
- (8) BBa
- (pCAGG-A44BBa) 80 81
- (9) aAA
- (pCAGG-A44aAA) 82 83
- (10) aBA
- (pCAGG-A44aBA) 84 85
- (11) AAA (G)
- (pCAGG-A44LG) 86 87
- (12) BBA (G)
- (pCAGG-A44BBAG) 88 89
- (13) BAA (G)
- (pCAGG-A44BAAG) 90 91
- (14) ABA (G)
- (pCAGG-A44ABAG) 92 93
- (15) AAa (G)
- (pCAGG-A44AAaG) 94 95
- (16) BAa (G)
- (pCAGG-A44BAaG) 96 97
- (17) ABa (G)
- (pAGG-A44ABaG) 98 99
- (18) BBa (G)
- (pCAGG-A44BBaG) 100 101
- (19) aAA (G)
- (pCAGG-A44aAAG) 102 103
- (20) aBA (G)
- (pAGG-A44aBAG) 104 105
[Ejemplo 19] Preparación de anticuerpos
Las células de la cepa HEK293 derivadas de células de carcinoma renal fetal humanas se suspendieron en medio DMEM (Invitrogen) que contenía FCS al 10% (Moregate), 6 x 106 células se colocaron en platos de 10 cm de 20 diámetro para células adherentes (Coming) y se cultivaron en una incubadora de CO2 (37°C, CO2 al 5%) durante la noche. Cualquiera de los vectores de expresión de cadena L del ejemplo 18, dos tipos del vector de expresión de cadena H (30 µg) de pCAGG-chiB26-g4b y pCAGG-chiA44-g4a o pCAGG-chiA69-g4a del ejemplo 17, y 1,5 mL de medio OPTI-MEMI se agregaron a la mezcla de 60 µL de reactivo de transfección Lipofectamine 2000 (Invitrogen) y 1,5 mL de medio Opti-MEM I (Invitrogen) y se dejó reposar a temperatura ambiente durante 20 minutos, y la mezcla
33
Claims (1)
-
imagen1 imagen2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005112514 | 2005-04-08 | ||
| JP2005112514 | 2005-04-08 | ||
| PCT/JP2006/306821 WO2006109592A1 (ja) | 2005-04-08 | 2006-03-31 | 血液凝固第viii因子の機能代替抗体 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2494921T3 true ES2494921T3 (es) | 2014-09-16 |
Family
ID=37086871
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES06730769.4T Expired - Lifetime ES2494921T3 (es) | 2005-04-08 | 2006-03-31 | Anticuerpo que sustituye la función del factor VIII de coagulación sanguínea |
Country Status (13)
| Country | Link |
|---|---|
| US (16) | US20100003254A1 (es) |
| EP (2) | EP2824183B1 (es) |
| JP (3) | JP4917024B2 (es) |
| CA (2) | CA2957144C (es) |
| CY (1) | CY1115702T1 (es) |
| DK (2) | DK1876236T3 (es) |
| ES (1) | ES2494921T3 (es) |
| NO (1) | NO348522B1 (es) |
| PL (1) | PL1876236T3 (es) |
| PT (1) | PT1876236E (es) |
| SI (1) | SI1876236T1 (es) |
| TW (1) | TW200714313A (es) |
| WO (1) | WO2006109592A1 (es) |
Families Citing this family (81)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4794301B2 (ja) * | 2003-06-11 | 2011-10-19 | 中外製薬株式会社 | 抗体の製造方法 |
| WO2005035753A1 (ja) | 2003-10-10 | 2005-04-21 | Chugai Seiyaku Kabushiki Kaisha | 機能蛋白質を代替する二重特異性抗体 |
| AU2003271186A1 (en) * | 2003-10-14 | 2005-04-27 | Chugai Seiyaku Kabushiki Kaisha | Double specific antibodies substituting for functional protein |
| AU2006232287B2 (en) | 2005-03-31 | 2011-10-06 | Chugai Seiyaku Kabushiki Kaisha | Methods for producing polypeptides by regulating polypeptide association |
| CN104761637B (zh) | 2006-03-31 | 2021-10-15 | 中外制药株式会社 | 调控抗体血液动力学的方法 |
| EP2009101B1 (en) | 2006-03-31 | 2017-10-25 | Chugai Seiyaku Kabushiki Kaisha | Antibody modification method for purifying bispecific antibody |
| KR101680906B1 (ko) | 2007-09-26 | 2016-11-30 | 추가이 세이야쿠 가부시키가이샤 | 항체 정상영역 개변체 |
| ES2595638T3 (es) * | 2007-09-26 | 2017-01-02 | Chugai Seiyaku Kabushiki Kaisha | Método para modificar el punto isoeléctrico de un anticuerpo mediante la sustitución de aminoácidos en una CDR |
| TW201634479A (zh) | 2007-12-05 | 2016-10-01 | 中外製藥股份有限公司 | 抗nr10抗體及其應用 |
| KR102057826B1 (ko) | 2008-04-11 | 2019-12-20 | 추가이 세이야쿠 가부시키가이샤 | 복수 분자의 항원에 반복 결합하는 항원 결합 분자 |
| TWI440469B (zh) * | 2008-09-26 | 2014-06-11 | Chugai Pharmaceutical Co Ltd | Improved antibody molecules |
| EP2826789A1 (en) | 2009-03-19 | 2015-01-21 | Chugai Seiyaku Kabushiki Kaisha | Antibody constant region variant |
| JP5717624B2 (ja) | 2009-03-19 | 2015-05-13 | 中外製薬株式会社 | 抗体定常領域改変体 |
| KR20120024763A (ko) | 2009-05-15 | 2012-03-14 | 추가이 세이야쿠 가부시키가이샤 | 항axl 항체 |
| US10150808B2 (en) | 2009-09-24 | 2018-12-11 | Chugai Seiyaku Kabushiki Kaisha | Modified antibody constant regions |
| US8518405B2 (en) | 2009-10-08 | 2013-08-27 | The University Of North Carolina At Charlotte | Tumor specific antibodies and uses therefor |
| CA2785414C (en) | 2009-12-25 | 2019-01-22 | Tomoyuki Igawa | Polypeptide modification method for purifying polypeptide multimers |
| AR080428A1 (es) | 2010-01-20 | 2012-04-11 | Chugai Pharmaceutical Co Ltd | Formulaciones liquidas estabilizadas contentivas de anticuerpos |
| KR101762467B1 (ko) | 2010-01-29 | 2017-07-27 | 도레이 카부시키가이샤 | 폴리락트산계 수지 시트 |
| WO2011108714A1 (ja) | 2010-03-04 | 2011-09-09 | 中外製薬株式会社 | 抗体定常領域改変体 |
| US9845362B2 (en) | 2010-10-08 | 2017-12-19 | The University Of North Carolina At Charlotte | Compositions comprising chimeric antigen receptors, T cells comprising the same, and methods of using the same |
| TWI452136B (zh) * | 2010-11-17 | 2014-09-11 | 中外製藥股份有限公司 | A multiple specific antigen-binding molecule that replaces the function of Factor VIII in blood coagulation |
| EP2647706B1 (en) | 2010-11-30 | 2023-05-17 | Chugai Seiyaku Kabushiki Kaisha | Antigen-binding molecule capable of binding to plurality of antigen molecules repeatedly |
| PT3434767T (pt) | 2010-11-30 | 2026-01-23 | Chugai Pharmaceutical Co Ltd | Agente terapêutico indutor de citotoxicidade |
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| BR112015006634B1 (pt) * | 2012-09-28 | 2022-06-14 | Chugai Seiyaku Kabushiki Kaisha | Método e kit para avaliação de reação de coagulação sanguínea |
| US9908944B2 (en) * | 2013-07-15 | 2018-03-06 | Novo Nordisk A/S | Antibodies that bind urokinase plasminogen activator |
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