WO2008090958A1 - Domain-exchanged recombinant antibody composition - Google Patents
Domain-exchanged recombinant antibody composition Download PDFInfo
- Publication number
- WO2008090958A1 WO2008090958A1 PCT/JP2008/050992 JP2008050992W WO2008090958A1 WO 2008090958 A1 WO2008090958 A1 WO 2008090958A1 JP 2008050992 W JP2008050992 W JP 2008050992W WO 2008090958 A1 WO2008090958 A1 WO 2008090958A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- antibody
- domain
- antibody composition
- recombinant antibody
- human igg1
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2887—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against CD20
-
- 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
-
- 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
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/72—Increased effector function due to an Fc-modification
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Life Sciences & Earth Sciences (AREA)
- Peptides Or Proteins (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Disclosed are: a recombinant antibody composition which has the substitution of polypeptides respectively comprising CH1 domain and CH2 domain of the constant region in human IgG1 antibody by polypeptides respectively comprising amino acid sequences corresponding to the amino acid sequences located in the same positions in human IgG3 antibody as numbered according to the EU index as in Kabat et al. (hereinbelow, simply referred to as 'EU index'), and which has a higher CDC activity than those of human IgG1 antibody and human IgG3 antibody and a protein A-binding activity equivalent to that of human IgG1 antibody; an antibody molecule contained in the recombinant antibody composition or DNA encoding the heavy-chain constant region of the antibody molecule; a transformant produced by introducing the DNA into a host cell; a method for producing a recombinant antibody composition by using the transformant; and a pharmaceutical agent comprising the antibody composition as an active ingredient.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007-013642 | 2007-01-24 | ||
JP2007013642 | 2007-01-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008090958A1 true WO2008090958A1 (en) | 2008-07-31 |
Family
ID=39644532
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2008/050992 WO2008090958A1 (en) | 2007-01-24 | 2008-01-24 | Domain-exchanged recombinant antibody composition |
Country Status (1)
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WO (1) | WO2008090958A1 (en) |
Cited By (19)
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---|---|---|---|---|
WO2011051349A1 (en) | 2009-10-27 | 2011-05-05 | Ucb Pharma S.A. | Antibodies to ion channels |
WO2011051350A1 (en) | 2009-10-27 | 2011-05-05 | Ucb Pharma S.A. | Function modifying nav 1.7 antibodies |
WO2011051351A1 (en) | 2009-10-27 | 2011-05-05 | Ucb Pharma S.A. | Method to generate antibodies to ion channels |
WO2011118739A1 (en) | 2010-03-26 | 2011-09-29 | 協和発酵キリン株式会社 | Novel antibody having modification site introduced therein, and antibody fragment |
WO2011123708A2 (en) | 2010-03-31 | 2011-10-06 | Ablexis Llc | Genetic engineering of non-human animals for the production of chimeric antibodies |
JP2012527234A (en) * | 2009-05-20 | 2012-11-08 | ファームアブサイン インコーポレイテッド | Novel forms of dual target antibodies and uses thereof |
US8986694B1 (en) | 2014-07-15 | 2015-03-24 | Kymab Limited | Targeting human nav1.7 variants for treatment of pain |
US8992927B1 (en) | 2014-07-15 | 2015-03-31 | Kymab Limited | Targeting human NAV1.7 variants for treatment of pain |
US9045545B1 (en) | 2014-07-15 | 2015-06-02 | Kymab Limited | Precision medicine by targeting PD-L1 variants for treatment of cancer |
US9062105B1 (en) | 2014-07-15 | 2015-06-23 | Kymab Limited | Precision Medicine by targeting VEGF-A variants for treatment of retinopathy |
US9067998B1 (en) | 2014-07-15 | 2015-06-30 | Kymab Limited | Targeting PD-1 variants for treatment of cancer |
US9234037B2 (en) | 2009-10-27 | 2016-01-12 | Ucb Biopharma Sprl | Method to generate antibodies to ion channels |
US9346873B2 (en) | 2008-09-30 | 2016-05-24 | Ablexis, Llc | Non-human mammals for the production of chimeric antibodies |
US10618955B2 (en) | 2014-07-15 | 2020-04-14 | Kymab Limited | Methods for treating neurodegenerative disease using anti-PD-1 antibodies |
US10759867B2 (en) | 2011-07-06 | 2020-09-01 | Genmab B.V. | Antibody variants and uses thereof |
US11180572B2 (en) | 2012-07-06 | 2021-11-23 | Genmab B.V. | Dimeric protein with triple mutations |
JP2021534801A (en) * | 2018-08-29 | 2021-12-16 | ユナイテッド バイオファーマ インコーポレイテッド | Afcosilized antibody and its manufacturing method |
US11753479B2 (en) | 2014-03-04 | 2023-09-12 | Kymab Limited | Nucleic acids encoding anti-OX40L antibodies |
US11779604B2 (en) | 2016-11-03 | 2023-10-10 | Kymab Limited | Antibodies, combinations comprising antibodies, biomarkers, uses and methods |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007011041A1 (en) * | 2005-07-22 | 2007-01-25 | Kyowa Hakko Kogyo Co., Ltd. | Genetically modified antibody composition |
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2008
- 2008-01-24 WO PCT/JP2008/050992 patent/WO2008090958A1/en active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2007011041A1 (en) * | 2005-07-22 | 2007-01-25 | Kyowa Hakko Kogyo Co., Ltd. | Genetically modified antibody composition |
Non-Patent Citations (7)
Title |
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BREKKE O.H. ET AL.: "HUMAN IgG3 CAN ADOPT THE DISULFIDE BOND PATTERN CHARACTERISTIC FOR IgG1 WITHOUT RESEMBLING IT IN COMPLEMENT MEDIATED CELL LYSIS", MOL. IMMUNOL., vol. 30, no. 16, 1993, pages 1419 - 1425, XP023935453, DOI: doi:10.1016/0161-5890(93)90103-I * |
DALL-ACQUA W.F. ET AL.: "Modulation of the Effector Functions of a human IgG1 through Engineering of Its Hinge Region", J. IMMUNOL., vol. 177, 2006, pages 1129 - 1138, XP002497452 * |
KATO K. ET AL.: "13C NMR study of the mode of interaction in solution of the B fragment of staphyloccal protein A and the Fc fragments of mouse immunoglobulin G", FEBS LETT., vol. 328, no. 1-2, 1993, pages 49 - 54, XP025652646, DOI: doi:10.1016/0014-5793(93)80963-U * |
SHIMIZU A. ET AL.: "1H NMR STUDIES OF THE Fc REGION OF HUMAN IgG1 AND IgG3 IMMUNOGLOBULINS: ASSIGNMENT OF HISTIDINE RESONANCES IN THE CH3 DOMAIN AND IDENTIFICATION OF IgG3 PROTEIN CARRYING G3m(st) ALLOTYPES", MOL. IMMUNOL., vol. 20, no. 2, 1983, pages 141 - 148, XP023786323, DOI: doi:10.1016/0161-5890(83)90124-4 * |
THOMMESEN J.E. ET AL.: "Lysine 322 in the human IgG3 CH2 domain is crucial for antibody dependent complement activation", MOL. IMMUNOL., vol. 37, 2000, pages 995 - 1004, XP002522213, DOI: doi:10.1016/S0161-5890(01)00010-4 * |
VAN LOGHEM E. ET A.: "Staphyloccocal Protein A and Human IgG Subclasses and Allotypes", SCAND. J. IMMUNOL., vol. 15, no. 3, 1982, pages 275 - 278, XP008112596, DOI: doi:10.1111/j.1365-3083.1982.tb00649.x * |
YAMANE-OHNUKI N. ET AL.: "Establishment of FUT8 Knockout Chinese Hamster Ovary Cells: An Ideal Host Cell Line for Producing Completely Defucosylated Antibodies With Enhanced Antibody-Dependent Cellular Cytotoxicity", BIOTECHNOL. BIOENG., vol. 87, no. 5, 2004, pages 614 - 622, XP002984450, DOI: doi:10.1002/bit.20151 * |
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