ES2689080T3 - Anticuerpos que se unen a TL1A y sus usos - Google Patents
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- ES2689080T3 ES2689080T3 ES13811986.2T ES13811986T ES2689080T3 ES 2689080 T3 ES2689080 T3 ES 2689080T3 ES 13811986 T ES13811986 T ES 13811986T ES 2689080 T3 ES2689080 T3 ES 2689080T3
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- C07—ORGANIC CHEMISTRY
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- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2878—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
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- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
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- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6849—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a receptor, a cell surface antigen or a cell surface determinant
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- 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
- C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2875—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF/TNF superfamily, e.g. CD70, CD95L, CD153, CD154
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
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- 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
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- 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
- C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
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- 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
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/94—Stability, e.g. half-life, pH, temperature or enzyme-resistance
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Abstract
Un anticuerpo o fragmento del mismo que se une a TL1A humano, murino, de rata y de cynomolgus que comprende una CDR1 de cadena pesada que comprende la secuencia de aminoácidos de SEQ ID NO: 51, una CDR2 de cadena pesada que comprende la secuencia de aminoácidos de SEQ ID NO: 52, y una CDR3 de pesada cadena que comprende la secuencia de aminoácidos de SEQ ID NO: 53; y que comprende una CDR1 de cadena ligera que comprende la secuencia de aminoácidos de SEQ ID NO: 54, una CDR2 de cadena ligera que comprende la secuencia de aminoácidos de SEQ ID NO: 55, y una CDR3 de cadena ligera que comprende la secuencia de aminoácidos de SEQ ID NO: 56.
Description
una sustitución de aminoácidos. Típicamente, no se realizan más de dos, más preferiblemente no más de una y más preferiblemente, ninguna modificación de aminoácidos dentro de una región marco. En algunas realizaciones, la presente descripción proporciona un anticuerpo o fragmento del mismo, en el que la modificación de aminoácidos de las regiones marco de la secuencia de la región variable de cadena ligera comprende una sustitución de 5 aminoácidos en la posición aminoacídica seleccionada del grupo que consiste en 5 y 34. Las modificaciones aminoacídicas de las regiones marco de la secuencia de la región variable de cadena ligera comprenden una sustitución seleccionada del grupo que consiste en 5N y 34S, preferiblemente T5N y N34S, y en donde la posición aminoacídica de cada miembro del grupo se indica según la numeración de Kabat. En algunas realizaciones, el anticuerpo o fragmento del mismo de la presente invención puede comprender modificaciones de aminoácidos de
10 las regiones marco de la secuencia de región variable de cadena pesada como se ha expuesto anteriormente, y modificaciones de aminoácidos de las regiones marco de la secuencia de la región variable de cadena ligera como se ha expuesto anteriormente.
La presente descripción también proporciona un anticuerpo o fragmento del mismo que se une al TL1A que
15 comprende una región variable de cadena pesada seleccionada del grupo que consiste en SEQ ID NOS: 13, 26, 27, 28 y 29, preferiblemente seleccionada del grupo que consiste en SEQ ID NOS: 26, 27, 28 y 29, más preferiblemente del grupo que consiste en SEQ ID NOS: 27, 28 y 29 e incluso más preferiblemente del grupo que consiste en SEQ ID NOS: 27 y 29. La presente descripción también proporciona un anticuerpo o fragmento del mismo que se une al TL1A que comprende una región variable de cadena ligera seleccionada del grupo que consiste en SEQ ID NOS: 14
20 y 30, más preferiblemente SEQ ID NO: 14. En algunas realizaciones, el anticuerpo o fragmento del mismo que se une al TL1A comprende una región variable de cadena pesada seleccionada del grupo que consiste en SEQ ID NOS: 26, 27, 28 y 29, y una región variable de cadena ligera seleccionada del grupo que consiste en SEQ ID NOS: 14 y 30. Dado que cada una de estas secuencias de la región variable de cadena pesada y ligera se puede unir al TL1A, las secuencias de la región variable de cadena pesada y ligera se pueden "mezclar y combinar" para crear
25 moléculas de unión anti-TL1A de la invención. La unión a TL1A de dichos anticuerpos "mezclados y combinados" se puede analizar usando los ensayos de unión descritos, por ejemplo, en los Ejemplos.
En algunas realizaciones, el anticuerpo o fragmento del mismo que se une al TL1A comprende una región variable de cadena pesada seleccionada del grupo que consiste en SEQ ID NOS: 27 y 29, y una región variable de cadena 30 ligera seleccionada del grupo que consiste en SEQ ID NOS: 14 y 30. En realizaciones más preferidas, el anticuerpo
o fragmento del mismo que se une al TL1A comprende una región variable de cadena pesada que comprende la secuencia de aminoácidos de SEQ ID NO: 27, y una región variable de cadena ligera que comprende la secuencia de aminoácidos de SEQ ID NO: 14 o una región variable de cadena pesada que comprende la secuencia de aminoácidos de SEQ ID NO: 29, y una región variable de cadena ligera que comprende la secuencia de
35 aminoácidos de SEQ ID NO: 14. Mucho más preferido es un anticuerpo o fragmento del mismo que se une al TL1A que comprende una región variable de cadena pesada seleccionada del grupo que consiste en SEQ ID NOS: 27 y 29, y una región variable de cadena ligera que comprende la secuencia de aminoácidos de SEQ ID NO: 14.
La presente descripción también proporciona un anticuerpo o fragmento del mismo que se une al TL1A que
40 comprende una secuencia de cadena pesada seleccionada del grupo que consiste en SEQ ID NOS: 16, 21, 22, 23 y 24, preferiblemente seleccionada del grupo que consiste en SEQ ID NOS: 22, 23 y 24 y más preferiblemente del grupo que consiste en SEQ ID NOS: 22 y 24. La presente descripción también proporciona un anticuerpo o fragmento del mismo que se une al TL1A que comprende una secuencia de cadena ligera seleccionada del grupo que consiste en SEQ ID NOS: 17 y 25, más preferiblemente SEQ ID NO: 17. En algunas realizaciones, el anticuerpo
45 o fragmento del mismo que se une al TL1A comprende una secuencia de cadena pesada seleccionada del grupo que consiste en SEQ ID NOS: 21, 22, 23 y 24, y una secuencia de cadena ligera seleccionada del grupo que consiste en SEQ ID NOS: 17 y 25. Dado que cada una de estas secuencias de la región variable de cadena pesada y ligera se puede unir al TL1A, las secuencias de la región variable de cadena pesada y ligera se pueden "mezclar y combinar" para crear moléculas de unión anti-TL1A de la invención. La unión a TL1A de dichos anticuerpos
50 "mezclados y combinados" se puede analizar usando los ensayos de unión descritos, por ejemplo, en los Ejemplos.
En algunas realizaciones, el anticuerpo o fragmento del mismo que se une al TL1A comprende una secuencia de cadena pesada seleccionada del grupo que consiste en SEQ ID NOS: 22 y 24, y una secuencia de cadena ligera seleccionada del grupo que consiste en SEQ ID NOS: 17 y 25. En realizaciones más preferidas, el anticuerpo o 55 fragmento del mismo que se une al TL1A comprende una secuencia de cadena pesada que comprende la secuencia de aminoácidos de SEQ ID NO: 22, y una secuencia de cadena ligera que comprende la secuencia de aminoácidos de SEQ ID NO: 17 o una secuencia de cadena pesada que comprende la secuencia de aminoácidos de SEQ ID NO: 24, y una secuencia de cadena ligera que comprende la secuencia de aminoácidos de SEQ ID NO: 17. Mucho más preferido es un anticuerpo o fragmento del mismo que se une al TL1A que comprende una secuencia de cadena
17
Claims (1)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361748201P | 2013-01-02 | 2013-01-02 | |
| US201361748201P | 2013-01-02 | ||
| PCT/EP2013/077898 WO2014106602A1 (en) | 2013-01-02 | 2013-12-23 | Antibodies that bind to tl1a and their uses |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2689080T3 true ES2689080T3 (es) | 2018-11-08 |
Family
ID=49880804
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES13811986.2T Active ES2689080T3 (es) | 2013-01-02 | 2013-12-23 | Anticuerpos que se unen a TL1A y sus usos |
Country Status (22)
| Country | Link |
|---|---|
| US (3) | US9290576B2 (es) |
| EP (1) | EP2941302B1 (es) |
| JP (2) | JP2016503818A (es) |
| KR (1) | KR20150117259A (es) |
| CN (1) | CN105102067B (es) |
| AP (1) | AP2015008605A0 (es) |
| AU (2) | AU2013371957B2 (es) |
| CA (1) | CA2896894A1 (es) |
| CL (1) | CL2015001895A1 (es) |
| DK (1) | DK2941302T3 (es) |
| EA (1) | EA201591153A1 (es) |
| ES (1) | ES2689080T3 (es) |
| IL (2) | IL239634B (es) |
| MX (1) | MX360155B (es) |
| MY (1) | MY173334A (es) |
| PE (1) | PE20151289A1 (es) |
| PH (1) | PH12015501505B1 (es) |
| SG (1) | SG11201505186SA (es) |
| TR (1) | TR201815254T4 (es) |
| UA (1) | UA118961C2 (es) |
| WO (1) | WO2014106602A1 (es) |
| ZA (1) | ZA201505488B (es) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010062960A2 (en) | 2008-11-26 | 2010-06-03 | Cedars-Sinai Medical Center | METHODS OF DETERMINING RESPONSIVENESS TO ANTI-TNFα THERAPY IN INFLAMMATORY BOWEL DISEASE |
| MX2014003689A (es) | 2011-09-30 | 2014-12-05 | Teva Pharmaceuticals Australia Pty Ltd | Anticuerpos contra tl1a y sus usos. |
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