KR102103036B1 - 항-ｐｓｇｌ-１ 항체 및 그의 용도 - Google Patents
항-ｐｓｇｌ-１ 항체 및 그의 용도 Download PDFInfo
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- KR102103036B1 KR102103036B1 KR1020147000603A KR20147000603A KR102103036B1 KR 102103036 B1 KR102103036 B1 KR 102103036B1 KR 1020147000603 A KR1020147000603 A KR 1020147000603A KR 20147000603 A KR20147000603 A KR 20147000603A KR 102103036 B1 KR102103036 B1 KR 102103036B1
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| CN113667015B (zh) * | 2021-08-20 | 2022-10-11 | 北京康特泊瑞生物医药科技股份公司 | 靶向psgl-1蛋白的抗体及其用途 |
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|---|---|---|---|---|
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Family Cites Families (59)
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| GB8601597D0 (en) | 1986-01-23 | 1986-02-26 | Wilson R H | Nucleotide sequences |
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| US5464778A (en) | 1989-03-08 | 1995-11-07 | Board Of Regents Of The University Of Oklahoma | Glycoprotein ligand for P-selectin and methods of use thereof |
| US5690933A (en) | 1989-05-31 | 1997-11-25 | Glaxo Wellcome Inc. | Monoclonal antibodies for inducing tolerance |
| US5709859A (en) | 1991-01-24 | 1998-01-20 | Bristol-Myers Squibb Company | Mixed specificity fusion proteins |
| US6309639B1 (en) | 1991-02-05 | 2001-10-30 | The Board Of Regents Of The University Of Oklahoma | Method for inhibiting an inflammatory response using antibodies to P-selectin glycoprotein ligand |
| US6124267A (en) | 1991-02-05 | 2000-09-26 | Southpac Trust Internationals, Inc. | O-glycan inhibitors of selectin mediated inflammation derived from PSGL-1 |
| US5972625A (en) | 1991-05-06 | 1999-10-26 | The Regents Of The University Of California | Assays for inhibitors of leukocyte adhesion |
| ATE179210T1 (de) | 1992-03-17 | 1999-05-15 | Novartis Erfind Verwalt Gmbh | Gentechnologisch hergestellte antikörper |
| US6174666B1 (en) | 1992-03-27 | 2001-01-16 | The United States Of America As Represented By The Department Of Health And Human Services | Method of eliminating inhibitory/instability regions from mRNA |
| US5843707A (en) | 1992-10-23 | 1998-12-01 | Genetics Institute, Inc. | Nucleic acid encoding a novel P-selectin ligand protein |
| US6210671B1 (en) | 1992-12-01 | 2001-04-03 | Protein Design Labs, Inc. | Humanized antibodies reactive with L-selectin |
| WO1994014836A1 (en) | 1992-12-18 | 1994-07-07 | Centocor, Inc. | Peptide inhibitors of selectin binding |
| DK0689599T3 (da) | 1993-01-25 | 1999-08-16 | Dana Farber Cancer Inst Inc | Kimære selectiner ved udveksling af domæner og anvendelser deraf |
| WO1995014787A1 (en) | 1993-11-22 | 1995-06-01 | Centocor, Inc. | Peptide inhibitors of selecting binding |
| FR2716640B1 (fr) | 1994-02-28 | 1996-05-03 | Procedes Machines Speciales | Dispositif de centrage et de blocage d'une pièce en vue de son rodage à l'aide d'un rodoir à expansion. |
| KR100523506B1 (en) | 1995-08-03 | 2005-10-24 | Peptide and O-glycan inhibitors of selectin mediated inflammation | |
| US6348581B1 (en) | 1996-10-31 | 2002-02-19 | The Dow Chemical Company | High affinity humanized anti-TAG-72 monoclonalantibodies |
| WO1999043353A2 (en) | 1998-02-26 | 1999-09-02 | Boehringer Ingelheim Pharmaceuticals, Inc. | Combination anti-selectin and immunosuppressant therapy |
| DK1071700T3 (da) | 1998-04-20 | 2010-06-07 | Glycart Biotechnology Ag | Glykosylerings-modifikation af antistoffer til forbedring af antistofafhængig cellulær cytotoksicitet |
| BR9914957A (pt) | 1998-10-30 | 2001-07-24 | Genetics Inst | Inibição de células t citotóxicas por antagonistas de ligando de selectina-p (psgl) |
| AU3672800A (en) | 1999-04-09 | 2000-11-14 | Kyowa Hakko Kogyo Co. Ltd. | Method for controlling the activity of immunologically functional molecule |
| US6696620B2 (en) | 2000-05-02 | 2004-02-24 | Epicyte Pharmaceutical, Inc. | Immunoglobulin binding protein arrays in eukaryotic cells |
| AU2001261735B2 (en) | 2000-05-19 | 2006-09-21 | The Center For Blood Research, Inc. | Methods for diagnosing and treating hemostatic disorders by modulating p-selectin activity |
| EP1325123A4 (en) | 2000-09-12 | 2004-07-21 | Inst Genetics Llc | INHIBITION OF STENOSIS OR RESTENOSIS USING P-SELECTINE ANTAGONISTS |
| CA2433225A1 (en) | 2000-12-29 | 2002-07-11 | Bio-Technology General, Inc. | Isolated molecules comprising epitopes containing sulfated moieties, antibodies to such epitopes, and uses thereof |
| US20040002450A1 (en) | 2000-12-29 | 2004-01-01 | Janette Lazarovits | Y17 - isolated molecules comprising epitopes containing sulfated moieties, antibodies to such epitopes, and uses thereof |
| US20040001839A1 (en) | 2000-12-29 | 2004-01-01 | Avigdor Levanon | Multimers - isolated molecules comprising epitopes containing sulfated moieties, antibodies to such epitopes, and uses thereof |
| CA2385745C (en) | 2001-06-08 | 2015-02-17 | Abbott Laboratories (Bermuda) Ltd. | Methods of administering anti-tnf.alpha. antibodies |
| US6884619B2 (en) | 2001-07-17 | 2005-04-26 | Yale University | Inhibition of BEHAB cleavage and primary central nervous system (CNS) tumors |
| US20040116333A1 (en) | 2001-08-03 | 2004-06-17 | Rong-Hwa Lin | Modulators of P-selectin glycoprotein ligand 1 |
| US7744888B2 (en) | 2001-08-03 | 2010-06-29 | Abgenomics Cooperatief U.A. | Methods of modulating T cell or natural killer cell activity with anti-P-selectin glycoprotein ligand 1 antibodies |
| ATE430580T1 (de) | 2001-10-25 | 2009-05-15 | Genentech Inc | Glycoprotein-zusammensetzungen |
| JP2005536199A (ja) | 2002-07-01 | 2005-12-02 | サビエント ファーマシューティカルズ，インコーポレイティド | 抗体及びそれらの使用 |
| US9068234B2 (en) | 2003-01-21 | 2015-06-30 | Ptc Therapeutics, Inc. | Methods and agents for screening for compounds capable of modulating gene expression |
| KR20060107501A (ko) | 2003-06-30 | 2006-10-13 | 바이오-테크널러지 제너럴 (이스라엘) 리미티드 | 특이적인 인간 항체 |
| DK1707627T3 (da) * | 2003-12-25 | 2012-12-17 | Kyowa Hakko Kirin Co Ltd | Antagonistisk anti-CD40-antistofmutant. |
| EP1720996A4 (en) * | 2004-02-13 | 2007-03-21 | Immunomedics Inc | RECOMBINANT CYTOTOXIC RASES CONTAINING FUSION PROTEINS |
| UA105492C2 (uk) | 2004-05-11 | 2014-05-26 | Абдженомікс Коеператіеф У.А. | Спосіб одержання антитіла для викликання смерті активованих т-клітин, спосіб визначення прийнятної сполуки для викликання смерті активованих т-клітин та фармацевтична композиція |
| US7501121B2 (en) * | 2004-06-17 | 2009-03-10 | Wyeth | IL-13 binding agents |
| TWI309240B (en) * | 2004-09-17 | 2009-05-01 | Hoffmann La Roche | Anti-ox40l antibodies |
| TWI461436B (zh) | 2005-11-25 | 2014-11-21 | Kyowa Hakko Kirin Co Ltd | 人類ｃｄ１３４（ｏｘ４０）之人類單株抗體及其製造及使用方法 |
| TWI551607B (zh) * | 2006-07-14 | 2016-10-01 | Ａｃ免疫公司 | 人類化抗體 |
| NZ580553A (en) * | 2007-03-22 | 2012-05-25 | Genentech Inc | Apoptotic anti- ige antibodies binding the membrane-bound ige |
| ES2667863T3 (es) * | 2007-03-29 | 2018-05-14 | Genmab A/S | Anticuerpos biespecíficos y métodos de producción de los mismos |
| JP6071165B2 (ja) * | 2007-05-31 | 2017-02-01 | ゲンマブ エー／エス | 安定なＩｇＧ４抗体 |
| US9273134B2 (en) | 2007-06-05 | 2016-03-01 | Yale University | Inhibitors of receptor tyrosine kinases and methods of use thereof |
| CN101842117A (zh) * | 2007-08-28 | 2010-09-22 | 比奥根艾迪克Ma公司 | 抗igf-1r抗体及其用途 |
| JO3076B1 (ar) | 2007-10-17 | 2017-03-15 | Janssen Alzheimer Immunotherap | نظم العلاج المناعي المعتمد على حالة apoe |
| US8092804B2 (en) * | 2007-12-21 | 2012-01-10 | Medimmune Limited | Binding members for interleukin-4 receptor alpha (IL-4Rα)-173 |
| US20110086366A1 (en) * | 2008-02-22 | 2011-04-14 | Genmab A/S | Methods for assessing the risk of adverse events upon treatment with igg4 antibodies |
| WO2009140623A2 (en) * | 2008-05-15 | 2009-11-19 | Selexys Pharmaceuticals Corporation | Anti-psgl-1 antibodies and methods of identification and use |
| WO2010102792A2 (en) * | 2009-03-12 | 2010-09-16 | Imed Ab | Human antibodies against human fas and their use |
| IN2012DN00863A (enExample) * | 2009-07-31 | 2015-07-10 | Medarex Inc | |
| JP6180408B2 (ja) | 2011-06-13 | 2017-08-16 | アブゲノミクス コーペラティフ ユー．エー． | 抗ｐｓｇｌ−１抗体およびその使用 |
| KR20170063507A (ko) | 2014-06-20 | 2017-06-08 | 어브게노믹스 인터내셔널 인코포레이티드 | Her2 항체-약물 접합체 |
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100891620B1 (ko) * | 2004-04-13 | 2009-04-02 | 에프. 호프만-라 로슈 아게 | 항-ｐ-셀렉틴 항체 |
| WO2005110475A2 (en) * | 2004-05-10 | 2005-11-24 | Abgenomics Corporation | Antibodies |
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