ES2986097T3 - Proteínas de fusión de interleucina-2/receptor alfa de interleucina-2 y métodos de uso - Google Patents
Proteínas de fusión de interleucina-2/receptor alfa de interleucina-2 y métodos de uso Download PDFInfo
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- ES2986097T3 ES2986097T3 ES15750560T ES15750560T ES2986097T3 ES 2986097 T3 ES2986097 T3 ES 2986097T3 ES 15750560 T ES15750560 T ES 15750560T ES 15750560 T ES15750560 T ES 15750560T ES 2986097 T3 ES2986097 T3 ES 2986097T3
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| AU2018234810B2 (en) | 2017-03-15 | 2023-05-11 | Pandion Operations, Inc. | Targeted immunotolerance |
| US10676516B2 (en) | 2017-05-24 | 2020-06-09 | Pandion Therapeutics, Inc. | Targeted immunotolerance |
| WO2019113221A1 (en) * | 2017-12-06 | 2019-06-13 | The Board Of Trustees Of The Leland Stanford Junior University | Engineered proteins to enhance sensitivity of a cell to il-2 |
| US10174092B1 (en) | 2017-12-06 | 2019-01-08 | Pandion Therapeutics, Inc. | IL-2 muteins |
| USRE50550E1 (en) | 2017-12-06 | 2025-08-26 | Pandion Operations, Inc. | IL-2 muteins and uses thereof |
| US10946068B2 (en) | 2017-12-06 | 2021-03-16 | Pandion Operations, Inc. | IL-2 muteins and uses thereof |
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| JP7775078B2 (ja) * | 2019-03-18 | 2025-11-25 | バイオエヌテック セル アンド ジーン セラピーズ ゲーエムベーハー | 免疫エフェクタ細胞の特異的活性化のためのインターロイキン２受容体（ｉｌ２ｒ）およびインターロイキン２（ｉｌ２）バリアント |
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| WO2020236875A1 (en) | 2019-05-20 | 2020-11-26 | Pandion Therapeutics, Inc. | Madcam targeted immunotolerance |
| KR20220012256A (ko) * | 2019-05-24 | 2022-02-03 | 프로비바 테라퓨틱스 (홍콩) 리미티드 | Il-2 조성물 및 이의 사용 방법 |
| US11246906B2 (en) * | 2019-06-11 | 2022-02-15 | Alkermes Pharma Ireland Limited | Compositions and methods for subcutaneous administration of cancer immunotherapy |
| CN114450297A (zh) * | 2019-07-12 | 2022-05-06 | 普罗维瓦疗法香港有限公司 | Il-2组合物及其使用方法 |
| CN114466657B (zh) * | 2019-07-25 | 2024-11-15 | 芝加哥大学 | 包括蛋白酶激活治疗剂的组合物和方法 |
| US20220378933A1 (en) * | 2019-09-19 | 2022-12-01 | Proviva Therapeutics (Hong Kong) Limited | Il-2 compositions and methods of use thereof |
| CA3157229A1 (en) * | 2019-10-18 | 2021-04-22 | Alkermes Pharma Ireland Limited | Immunomodulatory il-2 agents in combination with immune checkpoint inhibitors |
| TW202136317A (zh) | 2019-12-20 | 2021-10-01 | 美商再生元醫藥公司 | 新穎之ｉｌ２促效劑及其使用方法（二） |
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| EP4143220A4 (en) | 2020-04-30 | 2024-05-29 | Immune Targeting Inc. | COMPOSITION OF ACTIVATABLE IL2 AND METHODS OF USE |
| JP7788447B2 (ja) * | 2020-08-13 | 2025-12-18 | ブリストル－マイヤーズ スクイブ カンパニー | 目的の細胞を標的とするためのｉｌ－２の向け直し方法 |
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| IL314734A (en) * | 2022-02-11 | 2024-10-01 | Mural Oncology Inc | Compositions and methods for cancer immunotherapy |
| EP4479090A4 (en) * | 2022-02-16 | 2025-08-27 | Univ Miami | IL-2 AND TL1A FUSION PROTEINS AND METHODS OF USE THEREOF |
| CN114875069B (zh) * | 2022-04-22 | 2023-09-15 | 四川大学 | 基因工程修饰的il2细胞因子的重组载体、宿主细胞及其用途 |
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Family Cites Families (22)
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| US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
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| FR2619719B1 (fr) | 1987-09-01 | 1991-05-10 | Sanofi Sa | Procede d'obtention d'interleukine-2 a partir de cellules eucaryotes, vecteurs necessaires a sa mise en oeuvre et lignees cellulaires hautement productrices |
| US5250296A (en) * | 1990-11-29 | 1993-10-05 | Takeda Chemical Industries, Ltd. | Immunostimulant agent containing interleukin-2 and 5'-deoxy-5-fluorouridine |
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| US5837458A (en) | 1994-02-17 | 1998-11-17 | Maxygen, Inc. | Methods and compositions for cellular and metabolic engineering |
| DE69530415T2 (de) | 1994-12-28 | 2004-02-12 | University Of Kentucky | Rekombinierte sequenzen des monoklonalen anti-idiotypischen antikörpers 3h1, diean dem menschlichen karzioembyonischen antigen liiert sind |
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| DZ2788A1 (fr) | 1998-05-15 | 2003-12-01 | Bayer Ag | Agonistes et antagonistes selectifs à IL-2. |
| CN1596311A (zh) | 2001-09-28 | 2005-03-16 | 株式会社载体研究所 | 编码表位结合型β2m且感染哺乳动物细胞的病毒载体及其应用 |
| RU2006135112A (ru) | 2004-03-05 | 2008-04-10 | Чирон Корпорейшн (Us) | Тест-система in vitro для прогнозирования устойчивости пациента к терапевтическим средствам |
| US8124084B2 (en) | 2005-05-17 | 2012-02-28 | University Of Connecticut | Compositions and methods for immunomodulation in an organism using IL-15 and soluble IL-15Ra |
| CN101255197B (zh) * | 2008-03-28 | 2012-01-25 | 浙江海正药业股份有限公司 | 血清白蛋白与白介素1受体拮抗剂的融合蛋白及应用 |
| GB0815216D0 (en) * | 2008-08-21 | 2008-09-24 | Asterion Ltd | Interleukin |
| WO2011123683A2 (en) * | 2010-04-02 | 2011-10-06 | University Of Rochester | Protease activated cytokines |
| WO2012088383A2 (en) | 2010-12-23 | 2012-06-28 | Genentech, Inc. | PILR alpha INTERACTIONS AND METHODS OF MODIFYING SAME |
| EP2858672B1 (en) * | 2012-06-08 | 2018-04-04 | Alkermes, Inc. | Fusion polypeptides comprising mucin-domain polypeptide linkers |
| US20140044675A1 (en) * | 2012-08-10 | 2014-02-13 | Roche Glycart Ag | Interleukin-2 fusion proteins and uses thereof |
| WO2014100913A1 (en) | 2012-12-24 | 2014-07-03 | Beijing Anxinhuaide Biotech. Co., Ltd | Improving the half life of a therapeutic polypeptide by fusing with a trimeric scaffold protein via a spacer |
| MA40094B1 (fr) | 2014-08-06 | 2022-05-31 | Univ Miami | Protéines de fusion de l'interleukine-2/récepteur alpha de l'interleukine-2 et procédés d'utilisation |
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