JP5070117B2 - Ｉｌ−１７相同的ポリペプチドとその治療上の用途 - Google Patents
Ｉｌ−１７相同的ポリペプチドとその治療上の用途 Download PDFInfo
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| US6562578B1 (en) | 1999-01-11 | 2003-05-13 | Schering Corporation | IL-17-like cytokine binding compounds and antibodies |
| DE69936382T3 (de) | 1998-05-15 | 2011-07-07 | Genentech, Inc., Calif. | Therapeutische verwendungen von il-17 homologe polypeptide |
| US7771719B1 (en) | 2000-01-11 | 2010-08-10 | Genentech, Inc. | Pharmaceutical compositions, kits, and therapeutic uses of antagonist antibodies to IL-17E |
| JP2003525251A (ja) * | 2000-02-29 | 2003-08-26 | ザイモジェネティクス，インコーポレイティド | シュワン細胞によるミエリンの産生を促進するための方法 |
| US7718397B2 (en) | 2000-03-21 | 2010-05-18 | Genentech, Inc. | Nucleic acids encoding receptor for IL-17 homologous polypeptides and uses thereof |
| US6676939B2 (en) * | 2000-04-18 | 2004-01-13 | Schering Corporation | Methods of modulating IL-174 response |
| EP1303604A2 (en) * | 2000-05-24 | 2003-04-23 | Schering Corporation | Mammalian receptor proteins; related reagents and methods |
| US20030096969A1 (en) | 2000-06-02 | 2003-05-22 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
| AU2001277980A1 (en) * | 2000-07-26 | 2002-02-05 | Zymogenetics Inc. | Human cytokine receptor |
| EP1529843A3 (en) * | 2000-08-11 | 2005-06-08 | Eli Lilly & Company | Novel secreted proteins and their uses |
| WO2002033083A2 (en) * | 2000-10-13 | 2002-04-25 | Eli Lilly And Company | Methods of using a human il-17-related polypeptide to treat disease |
| WO2002038764A2 (en) * | 2000-11-10 | 2002-05-16 | The Regents Of The University Of California | Il-17 receptor-like protein, uses thereof, and modulation of catabolic activity of il-17 cytokines on bone and cartilage |
| US20070160576A1 (en) | 2001-06-05 | 2007-07-12 | Genentech, Inc. | IL-17A/F heterologous polypeptides and therapeutic uses thereof |
| WO2003034984A2 (en) * | 2001-10-19 | 2003-05-01 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of inflammatory bowel disorders |
| JP2006512903A (ja) * | 2002-09-11 | 2006-04-20 | ジェネンテック・インコーポレーテッド | 免疫関連疾患の治療のための新規組成物と方法 |
| US20070048301A1 (en) * | 2002-11-26 | 2007-03-01 | Bodary-Winter Sarah C | Compositions and methods for the treatment of immune related diseases |
| WO2005051988A2 (en) * | 2003-03-03 | 2005-06-09 | Genentech, Inc. | Compositions and methods for the treatment of systemic lupus erythematosis |
| NZ573837A (en) | 2003-07-08 | 2010-07-30 | Genentech Inc | IL-17 A/F heterologous polypeptides and therapeutic uses thereof |
| WO2005051422A1 (en) | 2003-11-21 | 2005-06-09 | Celltech R & D Limited | Method for the treatment of multiple sclerosis by inhibiting il-17 activity |
| BRPI0510617A (pt) * | 2004-05-03 | 2007-10-30 | Schering Corp | uso de expressão de il-17 para prever inflamação de pele; processos de tratamento |
| US20050287593A1 (en) | 2004-05-03 | 2005-12-29 | Schering Corporation | Use of cytokine expression to predict skin inflammation; methods of treatment |
| CN101001871A (zh) | 2004-06-10 | 2007-07-18 | 津莫吉尼蒂克斯公司 | 可溶性ZcytoR14、抗ZcytoR14抗体和结合伴侣以及在炎症中的使用方法 |
| EP1799248B1 (en) * | 2004-09-21 | 2009-04-08 | Merck Serono SA | Use of il-17f for the treatment and/or prevention of neurologic diseases |
| JP2009505967A (ja) * | 2005-08-04 | 2009-02-12 | ザイモジェネティクス， インコーポレイテッド | Ｉｌ−１７ｂを用いた創傷の処置方法 |
| US20070249533A1 (en) | 2005-09-28 | 2007-10-25 | Levin Steven D | Il-17a and il-17f antagonists and methods of using the same |
| US7622116B2 (en) | 2006-02-10 | 2009-11-24 | Zymogenetics, Inc. | Method of treating inflammation using soluble IL-17RCX4 |
| CA2666426A1 (en) | 2006-10-26 | 2008-05-02 | Novo Nordisk A/S | Il-21 variants |
| WO2008073653A2 (en) * | 2006-11-08 | 2008-06-19 | Zymogenetics, Inc. | Il- 17b for use in wound healing |
| CN101679497A (zh) | 2007-03-26 | 2010-03-24 | 津莫吉尼蒂克斯公司 | 可溶性il-17ra/rc融合蛋白以及相关方法 |
| CN102083858B (zh) | 2008-05-05 | 2015-01-14 | 诺维莫尼公司 | 抗il-17a/il-17f交叉反应性抗体及其使用方法 |
| US8790642B2 (en) | 2008-08-29 | 2014-07-29 | Genentech, Inc. | Cross-reactive and bispecific anti-IL-17A/F antibodies |
| EP2406282A1 (en) | 2009-03-11 | 2012-01-18 | Novo Nordisk A/S | Interleukin-21 variants having antagonistic binding to the il-21 receptor |
| SG174891A1 (en) | 2009-04-01 | 2011-11-28 | Genentech Inc | Treatment of insulin-resistant disorders |
| GB0905972D0 (en) | 2009-04-06 | 2009-05-20 | Medical Res Council | Antibodies against IL-17BR |
| CN102458437B (zh) | 2009-05-05 | 2015-06-10 | 诺维莫尼公司 | 抗il-17f抗体及其使用方法 |
| WO2010142551A2 (en) * | 2009-06-12 | 2010-12-16 | Ablynx N.V. | Single variable domain (vhh) antibodies to cytokines of the il-17 receptor family |
| US20130323259A1 (en) | 2011-01-17 | 2013-12-05 | Novo Nordisk A/S | Il-21 ligands |
| UA117218C2 (uk) | 2011-05-05 | 2018-07-10 | Мерк Патент Гмбх | Поліпептид, спрямований проти il-17a, il-17f та/або il17-a/f |
| ES2669984T3 (es) | 2011-10-19 | 2018-05-29 | Morphosys Ag | Antagonistas de IL17C para el tratamiento de trastornos inflamatorios |
| JP6236948B2 (ja) * | 2013-07-17 | 2017-11-29 | 東ソー株式会社 | 抗体精製用溶出液および当該溶出液を用いた抗体精製方法 |
| KR20150050921A (ko) * | 2013-11-01 | 2015-05-11 | 현대중공업 주식회사 | 폐열 회수용 연관식 보일러 |
| EP3212665A2 (en) | 2014-10-31 | 2017-09-06 | F. Hoffmann-La Roche AG | Anti-il-17a and il-17f cross reactive antibody variants and compositions comprising and methods of making and using same |
| EP3250927B1 (en) | 2015-01-28 | 2020-02-19 | H. Hoffnabb-La Roche Ag | Gene expression markers and treatment of multiple sclerosis |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000073452A2 (en) * | 1999-06-02 | 2000-12-07 | Genentech, Inc. | Compositions and methods for the treatment of immune related diseases |
| KR100467998B1 (ko) * | 1995-03-23 | 2005-11-25 | 임뮤넥스 코포레이션 | Il-17수용체 |
| WO1999046281A2 (en) * | 1998-03-10 | 1999-09-16 | Genentech, Inc. | Novel polypeptides and nucleic acids encoding the same |
| WO1998049310A1 (en) * | 1997-04-25 | 1998-11-05 | Zymogenetics, Inc. | Mammalian cytokine-like factor 7 |
| WO1999003982A1 (en) * | 1997-07-16 | 1999-01-28 | Human Genome Sciences, Inc. | Interleukin-20 |
| US6482923B1 (en) * | 1997-09-17 | 2002-11-19 | Human Genome Sciences, Inc. | Interleukin 17-like receptor protein |
| AU9482498A (en) * | 1997-09-17 | 1999-04-05 | Human Genome Sciences, Inc. | Interleukin-17 receptor-like protein |
| AU2004799A (en) * | 1997-12-19 | 1999-07-12 | Millennium Biotherapeutics, Inc. | Novel embryo-derived interleukin related factor molecules and uses therefor |
| DE69936382T3 (de) * | 1998-05-15 | 2011-07-07 | Genentech, Inc., Calif. | Therapeutische verwendungen von il-17 homologe polypeptide |
| WO2000042187A1 (en) * | 1999-01-11 | 2000-07-20 | Schering Corporation | Interleukin-17 related mammalian cytokine (il-171). polynucleotides encoding them. uses |
| EP1141297B1 (en) * | 1999-01-11 | 2009-09-30 | Schering Corporation | Interleukin-17 related mammalian cytokines. polynucleotides encoding them . uses |
| AU2596700A (en) * | 1999-03-08 | 2000-09-28 | Genentech Inc. | Promotion or inhibition of angiogenesis and cardiovascularization |
| AU3632600A (en) * | 1999-05-14 | 2000-12-05 | Genentech Inc. | Compositions and methods for the treatment of immune related diseases |
| WO2001004304A1 (en) * | 1999-07-07 | 2001-01-18 | Zymogenetics, Inc. | Human cytokine receptor |
| JP2003527104A (ja) * | 1999-12-23 | 2003-09-16 | ジェネンテック・インコーポレーテッド | Ｉｌ−１７相同的ポリペプチドとその治療上の用途 |
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