RU2001114516A - PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF IMMUNE DISEASES - Google Patents

PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF IMMUNE DISEASES

Info

Publication number
RU2001114516A
RU2001114516A RU2001114516/14A RU2001114516A RU2001114516A RU 2001114516 A RU2001114516 A RU 2001114516A RU 2001114516/14 A RU2001114516/14 A RU 2001114516/14A RU 2001114516 A RU2001114516 A RU 2001114516A RU 2001114516 A RU2001114516 A RU 2001114516A
Authority
RU
Russia
Prior art keywords
pharmaceutical composition
ailim
substance
composition according
cytokine
Prior art date
Application number
RU2001114516/14A
Other languages
Russian (ru)
Other versions
RU2203682C2 (en
Inventor
Кацунари ТЕЗУКА
Йосихиро ВАТАНАБЕ
Рио АБЕ
Original Assignee
Джапан Тобакко Инк.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Джапан Тобакко Инк. filed Critical Джапан Тобакко Инк.
Publication of RU2001114516A publication Critical patent/RU2001114516A/en
Application granted granted Critical
Publication of RU2203682C2 publication Critical patent/RU2203682C2/en

Links

Claims (32)

1. Фармацевтическая композиция для предотвращения, лечения или профилактики артроза, содержащая вещество, обладающее активностью в модулировании сигнальной трансдукции, опосредованной AILIM, и фармацевтически приемлемый носитель.1. A pharmaceutical composition for preventing, treating or preventing arthrosis, comprising a substance having an activity in modulating signal transduction mediated by AILIM and a pharmaceutically acceptable carrier. 2. Фармацевтическая композиция по п. 1, в которой вещество обладает активностью в ингибировании пролиферации AILIM-экспрессирующих клеток или в ингибировании продукции цитокина AILIM-экспрессирующими клетками. 2. The pharmaceutical composition of claim 1, wherein the substance is active in inhibiting the proliferation of AILIM-expressing cells or in inhibiting the production of cytokine by AILIM-expressing cells. 3. Фармацевтическая композиция по п. 1 или 2, где цитокином является интерферон γ, который является цитокином, продуцируемым Т-клетками Thl-типа, или интерлейкин 4, который является цитокином, продуцируемым Т-клетками Th2-типа. 3. The pharmaceutical composition according to claim 1 or 2, wherein the cytokine is interferon γ, which is a cytokine produced by Thl-type T cells, or interleukin 4, which is a cytokine produced by Th2-type T cells. 4. Фармацевтическая композиция по любому из пп. 1-3, где артрозом является ревматоидный артрит. 4. The pharmaceutical composition according to any one of paragraphs. 1-3, where arthrosis is rheumatoid arthritis. 5. Фармацевтическая композиция по любому из пп. 1-3, где артрозом является остеоартрит. 5. The pharmaceutical composition according to any one of paragraphs. 1-3, where arthrosis is osteoarthritis. 6. Фармацевтическая композиция по любому из пп. 1-5, в которой веществом является белковое вещество. 6. The pharmaceutical composition according to any one of paragraphs. 1-5, in which the substance is a protein substance. 7. Фармацевтическая композиция по п. 6, в которой белковое вещество выбирают из группы, состоящей из a) антитела, которое связывается с AILIM или его частью; b) полипептида, содержащего полностью или частично внеклеточный район AILIM; с) слитого полипептида, содержащего полностью или частично внеклеточный район AILIM и полностью или частично константный район тяжелой цепи иммуноглобулина; и d) полипептида, который связывается с AILIM. 7. The pharmaceutical composition according to claim 6, in which the protein substance is selected from the group consisting of a) an antibody that binds to AILIM or part thereof; b) a polypeptide containing the whole or partially extracellular region of AILIM; c) a fusion polypeptide comprising a fully or partially extracellular region of AILIM and a fully or partially constant region of an immunoglobulin heavy chain; and d) a polypeptide that binds to AILIM. 8. Фармацевтическая композиция по любому из пп. 1-5, в которой веществом является небелковое вещество. 8. The pharmaceutical composition according to any one of paragraphs. 1-5, in which the substance is a non-protein substance. 9. Фармацевтическая композиция по п. 8, в которой небелковым веществом является ДНК, РНК или химически синтезируемое соединение. 9. The pharmaceutical composition of claim 8, wherein the non-proteinaceous substance is DNA, RNA, or a chemically synthesized compound. 10. Фармацевтическая композиция для предотвращения, лечения или профилактики воспаления, содержащая вещество, обладающее активностью в модулировании сигнальной трансдукции, опосредованной AILIM, и фармацевтически приемлемый носитель. 10. A pharmaceutical composition for preventing, treating, or preventing inflammation, comprising a substance having AILIM mediated signal transduction activity and a pharmaceutically acceptable carrier. 11. Фармацевтическая композиция по п. 10, в которой вещество обладает активностью в ингибировании пролиферации AILIM-экспрессирующих клеток или в ингибировании продукции цитокина AILIM-экспрессирующими клетками. 11. The pharmaceutical composition of claim 10, wherein the substance is active in inhibiting the proliferation of AILIM-expressing cells or in inhibiting cytokine production by AILIM-expressing cells. 12. Фармацевтическая композиция по п. 11, где цитокином является интерферон γ, который является цитокином, продуцируемым Т-клетками Thl-типа, или интерлейкин 4, который является цитокином, продуцируемым Т-клетками Th2-типа. 12. The pharmaceutical composition of claim 11, wherein the cytokine is interferon γ, which is a cytokine produced by Thl-type T cells, or interleukin 4, which is a cytokine produced by Th2-type T cells. 13. Фармацевтическая композиция по любому из пп. 10-12, где воспалением является гепатит. 13. The pharmaceutical composition according to any one of paragraphs. 10-12, where the inflammation is hepatitis. 14. Фармацевтическая композиция по любому из пп. 10-13, в которой веществом является белковое вещество. 14. The pharmaceutical composition according to any one of paragraphs. 10-13, in which the substance is a protein substance. 15. Фармацевтическая композиция по п. 14, в которой белковое вещество выбирают из группы, состоящей из а) антитела, которое связывается с AILIM или его частью; b) полипептида, содержащего полностью или частично внеклеточный район AILIM; c) слитого полипептида, содержащего полностью или частично внеклеточный район AILIM и полностью или частично константный район тяжелой цепи иммуноглобулина; и d) полипептида, который связывается с AILIM. 15. The pharmaceutical composition according to claim 14, in which the protein substance is selected from the group consisting of a) an antibody that binds to AILIM or part thereof; b) a polypeptide containing the whole or partially extracellular region of AILIM; c) a fusion polypeptide containing a fully or partially extracellular region of AILIM and a fully or partially constant region of an immunoglobulin heavy chain; and d) a polypeptide that binds to AILIM. 16. Фармацевтическая композиция по любому из пп. 10-13, в которой веществом является небелковое вещество. 16. The pharmaceutical composition according to any one of paragraphs. 10-13, in which the substance is a non-protein substance. 17. Фармацевтическая композиция по п. 16, в которой небелковым веществом является ДНК, РНК или химически синтезируемое соединение. 17. The pharmaceutical composition of claim 16, wherein the non-proteinaceous substance is DNA, RNA, or a chemically synthesized compound. 18. Фармацевтическая композиция для предотвращения, лечения или профилактики реакции трансплантат против хозяина и иммунного отторжения, сопровождающего реакцию трансплантат против хозяина или трансплантацию ткани или органа, содержащая вещество, обладающее активностью в модулировании сигнальной трансдукции, опосредованной AILIM, и фармацевтически приемлемый носитель. 18. A pharmaceutical composition for preventing, treating, or preventing a graft versus host reaction and immune rejection accompanying a graft versus host reaction or transplantation of a tissue or organ, comprising a substance having AILIM mediated signal transduction activity and a pharmaceutically acceptable carrier. 19. Фармацевтическая композиция по п. 18, в которой вещество обладает активностью в ингибировании пролиферации AILIM-экспрессирующих клеток или в ингибировании продукции цитокина AILIM-экспрессирующими клетками. 19. The pharmaceutical composition according to claim 18, in which the substance is active in inhibiting the proliferation of AILIM-expressing cells or in inhibiting the production of cytokine by AILIM-expressing cells. 20. Фармацевтическая композиция по п. 19, где цитокином является интерферон γ, который является цитокином, продуцируемым Т-клетками Thl-типа, или интерлейкин 4, который является цитокином, продуцируемым Т-клетками Th2-типа. 20. The pharmaceutical composition of claim 19, wherein the cytokine is interferon γ, which is a cytokine produced by Thl-type T cells, or interleukin 4, which is a cytokine produced by Th2-type T cells. 21. Фармацевтическая композиция по любому из пп. 18-20, в которой веществом является белковое вещество. 21. The pharmaceutical composition according to any one of paragraphs. 18-20, in which the substance is a protein substance. 22. Фармацевтическая композиция по п. 21, в которой белковое вещество выбирают из группы, состоящей из a) антитела, которое связывается с AILIM или его частью; b) полипептида, содержащего полностью или частично внеклеточный район AILIM; c) слитого полипептида, содержащего полностью или частично внеклеточный район AILIM и полностью или частично константный район тяжелой цепи иммуноглобулина; и d) полипептида, который связывается с AILIM. 22. The pharmaceutical composition according to p. 21, in which the protein substance is selected from the group consisting of a) an antibody that binds to AILIM or part thereof; b) a polypeptide containing the whole or partially extracellular region of AILIM; c) a fusion polypeptide comprising a fully or partially extracellular region of AILIM and a fully or partially constant region of an immunoglobulin heavy chain; and d) a polypeptide that binds to AILIM. 23. Фармацевтическая композиция по любому из пп. 18-20, в которой веществом является небелковое вещество. 23. The pharmaceutical composition according to any one of paragraphs. 18-20, in which the substance is a non-protein substance. 24. Фармацевтическая композиция по п. 23, в которой небелковым веществом является ДНК, РНК или химически синтезируемое соединение. 24. The pharmaceutical composition of claim 23, wherein the non-proteinaceous substance is DNA, RNA, or a chemically synthesized compound. 25. Фармацевтическая композиция для предотвращения иммунного ответа, запускаемого чужеродным антигеном или аутоантигеном, содержащая вещество, обладающее активностью в контролировании сигнальной трансдукции, опосредованной AILIM, и фармацевтически приемлемый носитель. 25. A pharmaceutical composition for preventing an immune response triggered by a foreign antigen or autoantigen, comprising a substance having activity in controlling signal transduction mediated by AILIM and a pharmaceutically acceptable carrier. 26. Фармацевтическая композиция по п. 25, где иммунным ответом является продукция антитела против антигена, пролиферация клеток или продукция цитокина. 26. The pharmaceutical composition of claim 25, wherein the immune response is production of an anti-antigen antibody, cell proliferation, or cytokine production. 27. Фармацевтическая композиция по п. 25 или 26, в которой вещество обладает активностью в ингибировании пролиферации AILIM-экспрессирующих клеток или в ингибировании продукции цитокина AILIM-экспрессирующими клетками. 27. The pharmaceutical composition according to p. 25 or 26, in which the substance has activity in inhibiting the proliferation of AILIM-expressing cells or in inhibiting the production of cytokine by AILIM-expressing cells. 28. Фармацевтическая композиция по п. 27, где цитокином является интерферон γ, который является цитокином, продуцируемым Т-клетками Thl-типа, или интерлейкин 4, который является цитокином, продуцируемым Т-клетками ТН2-типа. 28. The pharmaceutical composition of claim 27, wherein the cytokine is interferon γ, which is a cytokine produced by Thl type T cells, or interleukin 4, which is a cytokine produced by TH2 type T cells. 29. Фармацевтическая композиция по любому из пп. 25-28, в которой веществом является белковое вещество. 29. The pharmaceutical composition according to any one of paragraphs. 25-28, in which the substance is a protein substance. 30. Фармацевтическая композиция по п. 29, в которой белковое вещество выбирают из группы, состоящей из a) антитела, которое связывается с AILIM или его частью; b) полипептида, содержащего полностью или частично внеклеточный район AILIM; c) слитого полипептида, содержащего полностью или частично внеклеточный район ATLIM и полностью или частично константный район тяжелой цепи иммуноглобулина; и d) полипептида, который связывается с AILIM. 30. The pharmaceutical composition according to p. 29, in which the protein substance is selected from the group consisting of a) an antibody that binds to AILIM or part thereof; b) a polypeptide containing the whole or partially extracellular region of AILIM; c) a fusion polypeptide containing a fully or partially extracellular region of ATLIM and a fully or partially constant region of an immunoglobulin heavy chain; and d) a polypeptide that binds to AILIM. 31. Фармацевтическая композиция по любому из пп. 25-28, в которой веществом является небелковое вещество. 31. The pharmaceutical composition according to any one of paragraphs. 25-28, in which the substance is a non-protein substance. 32. Фармацевтическая композиция по п. 31, в которой небелковым веществом является ДНК, РНК или химически синтезируемое соединение. 32. The pharmaceutical composition according to p. 31, in which the non-protein substance is DNA, RNA or a chemically synthesized compound.
RU2001114516/14A 1999-08-30 2000-08-30 Pharmaceutical composition for immune disease treatment RU2203682C2 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP24267299 1999-08-30
JP11/242672 1999-08-30
JP2000/254680 2000-08-24
JP2000254680 2000-08-24

Publications (2)

Publication Number Publication Date
RU2001114516A true RU2001114516A (en) 2003-04-20
RU2203682C2 RU2203682C2 (en) 2003-05-10

Family

ID=26535864

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2001114516/14A RU2203682C2 (en) 1999-08-30 2000-08-30 Pharmaceutical composition for immune disease treatment

Country Status (21)

Country Link
US (2) US7465445B2 (en)
EP (1) EP1125585B1 (en)
JP (1) JP3871503B2 (en)
KR (2) KR100609441B1 (en)
CN (2) CN101028519B (en)
AT (1) ATE517925T1 (en)
AU (1) AU6865000A (en)
BR (1) BR0007047A (en)
CA (1) CA2348954C (en)
CZ (1) CZ304013B6 (en)
HK (1) HK1040489A1 (en)
HU (1) HU228575B1 (en)
ID (1) ID30042A (en)
IL (2) IL142691A0 (en)
NO (2) NO332264B1 (en)
NZ (1) NZ529577A (en)
RU (1) RU2203682C2 (en)
SK (1) SK288074B6 (en)
TR (1) TR200101205T1 (en)
WO (1) WO2001015732A1 (en)
ZA (1) ZA200103314B (en)

Families Citing this family (79)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7112655B1 (en) 1997-02-27 2006-09-26 Japan Tobacco, Inc. JTT-1 protein and methods of inhibiting lymphocyte activation
JP3521382B2 (en) 1997-02-27 2004-04-19 日本たばこ産業株式会社 Cell surface molecules that mediate cell-cell adhesion and signal transduction
US7435796B1 (en) 1999-02-03 2008-10-14 Amgen Inc. Antibodies which bind B7RP1
US7708993B2 (en) 1999-02-03 2010-05-04 Amgen Inc. Polypeptides involved in immune response
US8624010B1 (en) 1999-02-03 2014-01-07 Steven K. Yoshinaga Nucleic acids encoding B7RP1
JP5000804B2 (en) 1999-02-03 2012-08-15 アムジエン・インコーポレーテツド Novel polypeptides involved in immune responses
JP4210454B2 (en) 2001-03-27 2009-01-21 日本たばこ産業株式会社 Inflammatory bowel disease treatment
JP3871503B2 (en) 1999-08-30 2007-01-24 日本たばこ産業株式会社 Immune disease treatment
US7718644B2 (en) 2004-01-22 2010-05-18 The Trustees Of Columbia University In The City Of New York Anti-arrhythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) and uses thereof
US7879840B2 (en) 2005-08-25 2011-02-01 The Trustees Of Columbia University In The City Of New York Agents for preventing and treating disorders involving modulation of the RyR receptors
US8022058B2 (en) 2000-05-10 2011-09-20 The Trustees Of Columbia University In The City Of New York Agents for preventing and treating disorders involving modulation of the RyR receptors
JP3597140B2 (en) 2000-05-18 2004-12-02 日本たばこ産業株式会社 Human monoclonal antibody against costimulatory molecule AILIM and pharmaceutical use thereof
AU2002228610A8 (en) * 2000-11-22 2012-02-02 Univ Ohio State Agents for blocking t cell mediated immune reactions
JP4212278B2 (en) 2001-03-01 2009-01-21 日本たばこ産業株式会社 Graft rejection inhibitor
US8710045B2 (en) 2004-01-22 2014-04-29 The Trustees Of Columbia University In The City Of New York Agents for preventing and treating disorders involving modulation of the ryanodine receptors
US7704990B2 (en) 2005-08-25 2010-04-27 The Trustees Of Columbia University In The City Of New York Agents for preventing and treating disorders involving modulation of the RyR receptors
EP2737907A3 (en) * 2007-05-07 2014-11-05 MedImmune, LLC Anti-icos antibodies and their use in treatment of oncology, transplantation and autoimmune disease
ES2714381T3 (en) * 2011-03-31 2019-05-28 Inst Nat Sante Rech Med Antibodies directed against ICOS and their uses
DE102011006809A1 (en) 2011-04-05 2012-10-11 Freistaat Bayern vertreten durch die Julius-Maximilians-Universität Würzburg Use of an agent of antibodies and / or insulin-like growth factor antagonists
US9730960B2 (en) * 2011-06-09 2017-08-15 University Of Florida Research Foundation, Inc. Method for treating or preventing graft versus host disease
ES2684552T3 (en) 2012-09-03 2018-10-03 Inserm - Institut National De La Santé Et De La Recherche Médicale Antibodies directed against ICOS to treat graft versus host disease
US9458246B2 (en) 2013-03-13 2016-10-04 Amgen Inc. Proteins specific for BAFF and B7RP1
JOP20140087B1 (en) 2013-03-13 2021-08-17 Amgen Inc Proteins specific for baff and b7rp1 and uses thereof
GB201403775D0 (en) 2014-03-04 2014-04-16 Kymab Ltd Antibodies, uses & methods
MA41414A (en) 2015-01-28 2017-12-05 Centre Nat Rech Scient ICOS AGONIST BINDING PROTEINS
WO2017093933A1 (en) 2015-12-03 2017-06-08 Glaxosmithkline Intellectual Property Development Limited Cyclic purine dinucleotides as modulators of sting
WO2017098421A1 (en) 2015-12-08 2017-06-15 Glaxosmithkline Intellectual Property Development Limited Benzothiadiazine compounds
WO2017153952A1 (en) 2016-03-10 2017-09-14 Glaxosmithkline Intellectual Property Development Limited 5-sulfamoyl-2-hydroxybenzamide derivatives
EP3440072B1 (en) 2016-04-07 2020-01-29 GlaxoSmithKline Intellectual Property Development Ltd Heterocyclic amides useful as protein modulators
CN109608443B (en) 2016-04-07 2021-09-07 葛兰素史密斯克莱知识产权发展有限公司 Heterocyclic amides as protein modulators
WO2017191545A1 (en) 2016-05-05 2017-11-09 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
WO2018029474A2 (en) 2016-08-09 2018-02-15 Kymab Limited Anti-icos antibodies
US9567399B1 (en) 2016-06-20 2017-02-14 Kymab Limited Antibodies and immunocytokines
AU2017281830B2 (en) 2016-06-20 2023-04-06 Kymab Limited Anti-PD-L1 antibodies
EP3487503A1 (en) 2016-07-20 2019-05-29 GlaxoSmithKline Intellectual Property Development Limited Isoquinoline derivatives as perk inhibitors
EP3497128A2 (en) 2016-08-09 2019-06-19 Kymab Limited Anti-icos antibodies
US11779604B2 (en) 2016-11-03 2023-10-10 Kymab Limited Antibodies, combinations comprising antibodies, biomarkers, uses and methods
US11618785B2 (en) 2016-12-22 2023-04-04 Daiichi Sankyo Company, Limited Anti-CD3 antibody and molecules comprising the antibody
EP3585782A1 (en) 2017-02-27 2020-01-01 GlaxoSmithKline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors
TWI788340B (en) 2017-04-07 2023-01-01 美商必治妥美雅史谷比公司 Anti-icos agonist antibodies and uses thereof
CA3066038A1 (en) 2017-06-09 2018-12-13 Glaxosmithkline Intellectual Property Development Limited Combination therapy with icos agonist and ox40 agonist to treat cancer
CN110869049A (en) 2017-06-09 2020-03-06 葛兰素史克知识产权开发有限公司 Combination therapy
CA3066007A1 (en) 2017-06-09 2018-12-13 Glaxosmithkline Intellectual Property Development Limited Combination therapy with icos agonist and ox40 agonist to treat cancer
GB201709808D0 (en) 2017-06-20 2017-08-02 Kymab Ltd Antibodies
WO2019021208A1 (en) 2017-07-27 2019-01-31 Glaxosmithkline Intellectual Property Development Limited Indazole derivatives useful as perk inhibitors
WO2019053617A1 (en) 2017-09-12 2019-03-21 Glaxosmithkline Intellectual Property Development Limited Chemical compounds
WO2019053613A2 (en) 2017-09-14 2019-03-21 Glaxosmithkline Intellectual Property Development Limited Combination treatment for cancer
TW201927771A (en) 2017-10-05 2019-07-16 英商葛蘭素史密斯克藍智慧財產發展有限公司 Heterocyclic amides useful as protein modulators and methods of using the same
BR112020006780A2 (en) 2017-10-05 2020-10-06 Glaxosmithkline Intellectual Property Development Limited modulators of the interferon gene stimulator (sting)
GB201721338D0 (en) 2017-12-19 2018-01-31 Kymab Ltd Anti-icos Antibodies
US11629189B2 (en) 2017-12-19 2023-04-18 Kymab Limited Bispecific antibody for ICOS and PD-L1
GB201807924D0 (en) 2018-05-16 2018-06-27 Ctxt Pty Ltd Compounds
CN112469441A (en) 2018-05-31 2021-03-09 葛兰素史克知识产权开发有限公司 Combination therapy with ICOS binding protein and arginine methyltransferase inhibitors
CN112469416A (en) 2018-05-31 2021-03-09 葛兰素史克知识产权开发有限公司 Combination of type II protein arginine methyltransferase inhibitors and ICOS binding proteins for the treatment of cancer
EP3806848A2 (en) 2018-06-15 2021-04-21 Flagship Pioneering Innovations V, Inc. Increasing immune activity through modulation of postcellular signaling factors
WO2020031087A1 (en) 2018-08-06 2020-02-13 Glaxosmithkline Intellectual Property Development Limited Combination therapy
JP2022513374A (en) 2018-10-22 2022-02-07 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッド dosage
EP3962493A2 (en) 2019-05-03 2022-03-09 Flagship Pioneering Innovations V, Inc. Methods of modulating immune activity/level of irf or sting or of treating cancer, comprising the administration of a sting modulator and/or purinergic receptor modulator or postcellular signaling factor
GB201910305D0 (en) 2019-07-18 2019-09-04 Ctxt Pty Ltd Compounds
GB201910304D0 (en) 2019-07-18 2019-09-04 Ctxt Pty Ltd Compounds
WO2021018941A1 (en) 2019-07-31 2021-02-04 Glaxosmithkline Intellectual Property Development Limited Methods of treating cancer
WO2021046289A1 (en) 2019-09-06 2021-03-11 Glaxosmithkline Intellectual Property Development Limited Dosing regimen for the treatment of cancer with an anti icos agonistic antibody and ipilimumab
WO2021043961A1 (en) 2019-09-06 2021-03-11 Glaxosmithkline Intellectual Property Development Limited Dosing regimen for the treatment of cancer with an anti icos agonistic antibody and chemotherapy
EP4034562A2 (en) 2019-09-27 2022-08-03 GlaxoSmithKline Intellectual Property Development Limited Antigen binding proteins
EP4076434A1 (en) 2019-12-17 2022-10-26 Flagship Pioneering Innovations V, Inc. Combination anti-cancer therapies with inducers of iron-dependent cellular disassembly
US20230149543A1 (en) 2020-04-14 2023-05-18 Glaxosmithkline Intellectual Property Development Limited Combination treatment for cancer based upon an icos antbody and a pd-l1 antibody tgf-bets-receptor fusion protein
CN115698075A (en) 2020-04-14 2023-02-03 葛兰素史密斯克莱知识产权发展有限公司 Combination therapy of cancer involving anti-ICOS and anti-PD 1 antibodies, optionally further involving anti-TIM 3 antibodies
US20230131598A1 (en) 2020-04-14 2023-04-27 Glaxosmithkline Intellectual Property Development Limited Combination treatment for cancer
GB202007099D0 (en) 2020-05-14 2020-07-01 Kymab Ltd Tumour biomarkers for immunotherapy
CN116096906A (en) 2020-06-29 2023-05-09 旗舰创业创新五公司 Virus engineered to promote saenox delivery and use thereof in treating cancer
JP2024509529A (en) 2021-03-02 2024-03-04 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッド Substituted pyridines as DNMT1 inhibitors
WO2022212784A1 (en) 2021-03-31 2022-10-06 Flagship Pioneering Innovations V, Inc. Thanotransmission polypeptides and their use in treating cancer
WO2022208353A1 (en) 2021-03-31 2022-10-06 Glaxosmithkline Intellectual Property Development Limited Antigen binding proteins and combinations thereof
US20220396623A1 (en) 2021-05-18 2022-12-15 Kymab Limited Uses of anti-icos antibodies
GB202107994D0 (en) 2021-06-04 2021-07-21 Kymab Ltd Treatment of cancer
AU2022303363A1 (en) 2021-06-29 2024-01-18 Flagship Pioneering Innovations V, Inc. Immune cells engineered to promote thanotransmission and uses thereof
WO2023222854A1 (en) 2022-05-18 2023-11-23 Kymab Limited Uses of anti-icos antibodies
WO2024077191A1 (en) 2022-10-05 2024-04-11 Flagship Pioneering Innovations V, Inc. Nucleic acid molecules encoding trif and additionalpolypeptides and their use in treating cancer
WO2024151687A1 (en) 2023-01-09 2024-07-18 Flagship Pioneering Innovations V, Inc. Genetic switches and their use in treating cancer

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5506126A (en) 1988-02-25 1996-04-09 The General Hospital Corporation Rapid immunoselection cloning method
US6075181A (en) 1990-01-12 2000-06-13 Abgenix, Inc. Human antibodies derived from immunized xenomice
US5521288A (en) 1990-03-26 1996-05-28 Bristol-Myers Squibb Company CD28IG fusion protein
US5770197A (en) 1991-06-27 1998-06-23 Bristol-Myers Squibb Company Methods for regulating the immune response using B7 binding molecules and IL4-binding molecules
JP3162438B2 (en) 1991-09-12 2001-04-25 住友製薬株式会社 Highly sensitive specific antibody assay
US5484892A (en) 1993-05-21 1996-01-16 Dana-Farber Cancer Institute, Inc. Monoclonal antibodies that block ligand binding to the CD22 receptor in mature B cells
US6719972B1 (en) 1994-06-03 2004-04-13 Repligen Corporation Methods of inhibiting T cell proliferation or IL-2 accumulation with CTLA4- specific antibodies
US5747461A (en) 1994-07-26 1998-05-05 Markov; Angel K. Synergistic administration of cyclosporine and fructose diphosphate
US6440418B1 (en) * 1995-11-07 2002-08-27 Idec Pharmaceuticals Corporation Methods of treating autoimmune diseases with gp39-specific antibodies
US5914112A (en) 1996-01-23 1999-06-22 Genentech, Inc. Anti-CD18 antibodies in stroke
PT877626E (en) 1996-01-23 2003-01-31 Univ Vermont And State Agric C ANTI-CD1 ANTIBODIES FOR USE AGAINST ICTO
AU723669B2 (en) 1996-09-18 2000-08-31 Zetesis S.P.A Use of proteins as agents against autoimmune diseases
CA2270922A1 (en) 1996-11-08 1998-05-14 Idec Pharmaceuticals Corporation Identification of unique binding interactions between certain antibodies and the human b7.1 and b7.2 co-stimulatory antigens
CA2194814A1 (en) * 1997-01-10 1998-07-10 Terry L. Delovitch Stimulation of protective t cells to prevent autoimmune disease
AU4145597A (en) 1997-02-20 1998-09-09 Cedars-Sinai Medical Center Ulcerative colitis panca secretory vesicle antigen and methods of using sa me
JP3521382B2 (en) 1997-02-27 2004-04-19 日本たばこ産業株式会社 Cell surface molecules that mediate cell-cell adhesion and signal transduction
US7112655B1 (en) 1997-02-27 2006-09-26 Japan Tobacco, Inc. JTT-1 protein and methods of inhibiting lymphocyte activation
EP1787999B1 (en) 1997-04-07 2010-08-04 Genentech, Inc. Anti-VEGF antibodies
BR9809641A (en) * 1997-05-17 2000-07-11 Biogen Inc Use of a cd40: cd154 link switch to prevent inappropriate immune responses, particularly graft rejection
DE19821060A1 (en) 1997-09-23 1999-04-15 Bundesrepublik Deutschland Let T cell co-stimulating polypeptide, monoclonal antibodies, and the production and use thereof
EP1017723B1 (en) 1997-09-23 2007-01-10 Bundesrepublik Deutschland letztvertreten durch Den Direktor des Robert-Koch-Instituts Costimulating t-cell polypeptide, monoclonal antibodies, their preparation and use
JPH11228442A (en) 1998-02-09 1999-08-24 Cypros Pharmaceut Corp Use of fructose diphosphate for reducing cyclosporin dose after organ transplantation
JP2000154151A (en) 1998-09-14 2000-06-06 Kyo Jo Immunosuppressant
AU767241B2 (en) 1998-09-14 2003-11-06 Qiang Xu Immunosuppressive agents
WO2000019988A1 (en) 1998-10-07 2000-04-13 Millennium Pharmaceuticals, Inc. NOVEL Th2-SPECIFIC MOLECULES AND USES THEREOF
JP5000804B2 (en) 1999-02-03 2012-08-15 アムジエン・インコーポレーテツド Novel polypeptides involved in immune responses
PL360915A1 (en) 1999-05-06 2004-09-20 Genetics Institute, Llc Use of soluble costimulatory molecules to enhance immune responses
US6613327B1 (en) 1999-07-28 2003-09-02 Genetics Institute, Inc. Methods of preventing immune-mediated abortion by inhibiting a CD28-mediated costimulatory signal
AU6458400A (en) 1999-08-11 2001-03-13 Isis Innovation Limited Nucleic acid, polypeptides, assays, therapeutic methods and means
JP4210454B2 (en) 2001-03-27 2009-01-21 日本たばこ産業株式会社 Inflammatory bowel disease treatment
JP3871503B2 (en) 1999-08-30 2007-01-24 日本たばこ産業株式会社 Immune disease treatment
EP1212343A4 (en) 1999-09-03 2004-11-03 Human Genome Sciences Inc 52 human secreted proteins
EP1218504B1 (en) 1999-09-21 2007-07-11 Genetics Institute, LLC Gl50 molecules and uses therefor
AU1342501A (en) 1999-10-29 2001-05-14 Human Genome Sciences, Inc. 32 human secreted proteins
AU2001245396A1 (en) 2000-03-02 2001-09-12 Mayo Foundation For Medical Education And Research Hb7-h2, a novel co-stimulatory molecule
JP3597140B2 (en) * 2000-05-18 2004-12-02 日本たばこ産業株式会社 Human monoclonal antibody against costimulatory molecule AILIM and pharmaceutical use thereof
EP1337634A2 (en) 2000-11-28 2003-08-27 Amgen Inc. Novel polypeptides involved in immune response
JP4212278B2 (en) 2001-03-01 2009-01-21 日本たばこ産業株式会社 Graft rejection inhibitor

Similar Documents

Publication Publication Date Title
RU2001114516A (en) PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF IMMUNE DISEASES
CA2348954A1 (en) A pharmaceutical composition for treating immune diseases
De Maeyer et al. Interferon-γ
Suematsu et al. IgG1 plasmacytosis in interleukin 6 transgenic mice.
DeForge et al. Kinetics of TNF, IL-6, and IL-8 gene expression in LPS-stimulated human whole blood
Satoh et al. Recombinant human tumor necrosis factor alpha suppresses autoimmune diabetes in nonobese diabetic mice.
Ridderstad et al. Cytokines in rheumatoid arthritis
Noma et al. Enhancement of the interleukin 2 receptor expression on T cells by multiple B-lymphotropic lymphokines
Rolink et al. Monoclonal antibodies reactive with the mouse interleukin 5 receptor.
Rothman et al. Mitogen plus interleukin 4 induction of C epsilon transcripts in B lymphoid cells.
Honda et al. Quantitative analysis of serum IL-6 and its correlation with increased levels of serum IL-2R in HIV-induced diseases.
Rieckmann et al. Tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) in B-lymphocyte function
KR950016781A (en) Immunoconjugate
BG60256B1 (en) RECOMBINANT METHOD FOR LYMPHOTOXIN
Lernhardt et al. T-cell hybridomas which produce B lymphocyte replication factors only
CA2034741A1 (en) Therapeutic antibody based fusion proteins
CA2011893A1 (en) Pharmaceutical product for the treatment of immunoregulatory disorders
KR890009978A (en) Immobilized Interleukin2 and Interleukin2 Containing an Extended Peptide at the Carboxyl-Terminal
Ralph et al. Role of interleukin 2, interleukin 4, and alpha, beta, and gamma interferon in stimulating macrophage antibody-dependent tumoricidal activity.
Tucci et al. Effects of eleven cytokines and of IL-1 and tumor necrosis factor inhibitors in a human B cell assay.
SI9720013A (en) Modulation of TH1/TH2 cytokine expression by ribavirin and ribavirin analogs in activated T-lymphocytes
Alheim et al. Interleukin 1 expression is inducible by nerve growth factor in PC12 pheochromocytoma cells.
Fernandez-Botran et al. Methods in cellular immunology
Nguyen et al. Interleukin (IL)-15 enhances antibody-dependent cellular cytotoxicity and natural killer activity in neonatal cells
Adalid-Peralta et al. Stimulation of the primary anti-HIV antibody response by IFN-α in patients with acute HIV-1 infection