WO2008093688A1 - キメラFcγレセプター及び該レセプターを用いたADCC活性測定方法 - Google Patents

キメラFcγレセプター及び該レセプターを用いたADCC活性測定方法 Download PDF

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Publication number
WO2008093688A1
WO2008093688A1 PCT/JP2008/051333 JP2008051333W WO2008093688A1 WO 2008093688 A1 WO2008093688 A1 WO 2008093688A1 JP 2008051333 W JP2008051333 W JP 2008051333W WO 2008093688 A1 WO2008093688 A1 WO 2008093688A1
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receptor
chimeric
fcγ
adcc activity
human
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French (fr)
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Shigeto Kawai
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Forerunner Pharma Research Co Ltd
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Forerunner Pharma Research Co Ltd
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Priority to US12/525,031 priority Critical patent/US8946385B2/en
Priority to AT08704115T priority patent/ATE504647T1/de
Priority to DE602008006041T priority patent/DE602008006041D1/de
Priority to JP2008556119A priority patent/JP5299902B2/ja
Priority to EP08704115A priority patent/EP2123754B1/en
Publication of WO2008093688A1 publication Critical patent/WO2008093688A1/ja
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Priority to US14/556,684 priority patent/US9733245B2/en
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/566—Immunoassay; Biospecific binding assay; Materials therefor using specific carrier or receptor proteins as ligand binding reagents where possible specific carrier or receptor proteins are classified with their target compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70503—Immunoglobulin superfamily
    • C07K14/70535—Fc-receptors, e.g. CD16, CD32, CD64 (CD2314/705F)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
    • G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • G01N33/5014—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing toxicity
    • 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
    • C07K2317/40—Immunoglobulins specific features characterized by post-translational modification
    • C07K2317/41—Glycosylation, sialylation, or fucosylation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/52—Constant or Fc region; Isotype
    • 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
    • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C07K2317/732—Antibody-dependent cellular cytotoxicity [ADCC]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2500/00—Screening for compounds of potential therapeutic value
    • G01N2500/04—Screening involving studying the effect of compounds C directly on molecule A (e.g. C are potential ligands for a receptor A, or potential substrates for an enzyme A)
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2500/00—Screening for compounds of potential therapeutic value
    • G01N2500/10—Screening for compounds of potential therapeutic value involving cells

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
  • Toxicology (AREA)
  • Cell Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • General Physics & Mathematics (AREA)
  • Physics & Mathematics (AREA)
  • Biotechnology (AREA)
  • Pathology (AREA)
  • Microbiology (AREA)
  • Analytical Chemistry (AREA)
  • Food Science & Technology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Zoology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Peptides Or Proteins (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

 本発明は、マウスFcγレセプター細胞外領域とヒトFcγレセプター膜貫通領域を含むキメラレセプター、またはマウスFcγレセプター細胞外領域とヒトγ鎖膜貫通領域を含むキメラレセプターを提供することを課題とする。又、本発明は該キメラレセプターを用いたマウス抗体のADCC活性を測定する為の方法、ADCC活性を有するマウス抗体のスクリーニング方法を提供することを課題とする。  本発明者らは、上記の課題を解決するために、マウスFcγR3あるいはマウスFcγR4の細胞外領域と、ヒトγ鎖あるいはヒトFcγR3の膜貫通領域-細胞内領域を融合したキメラ分子を作製し、ヒトNK92細胞に発現させた。その結果、いずれの組み合わせのキメラレセプターでもADCC活性を誘導しうることが見出され、本発明のキメラレセプターにより、マウス抗体のADCC活性を測定することが可能であることを見出した。
PCT/JP2008/051333 2007-01-30 2008-01-30 キメラFcγレセプター及び該レセプターを用いたADCC活性測定方法 Ceased WO2008093688A1 (ja)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US12/525,031 US8946385B2 (en) 2007-01-30 2008-01-30 Chimeric Fcγ receptor and method for determination of ADCC activity by using the receptor
AT08704115T ATE504647T1 (de) 2007-01-30 2008-01-30 Chimärer fc gamma rezeptor und verfahren zur bestimmung von adcc-aktivität unter verwendung des rezeptors
DE602008006041T DE602008006041D1 (de) 2007-01-30 2008-01-30 CHIMÄRER Fc GAMMA REZEPTOR UND VERFAHREN ZUR BESTIMMUNG VON ADCC-AKTIVITÄT UNTER VERWENDUNG DES REZEPTORS
JP2008556119A JP5299902B2 (ja) 2007-01-30 2008-01-30 キメラFcγレセプター及び該レセプターを用いたADCC活性測定方法
EP08704115A EP2123754B1 (en) 2007-01-30 2008-01-30 CHIMERIC Fc GAMMA RECEPTOR AND METHOD FOR DETERMINATION OF ADCC ACTIVITY BY USING THE RECEPTOR
US14/556,684 US9733245B2 (en) 2007-01-30 2014-12-01 Chimeric Fc-gamma receptor and method for determination of ADCC activity by using the receptor

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007-020155 2007-01-30
JP2007020155 2007-01-30

Related Child Applications (2)

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US12/525,031 A-371-Of-International US8946385B2 (en) 2007-01-30 2008-01-30 Chimeric Fcγ receptor and method for determination of ADCC activity by using the receptor
US14/556,684 Division US9733245B2 (en) 2007-01-30 2014-12-01 Chimeric Fc-gamma receptor and method for determination of ADCC activity by using the receptor

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WO2008093688A1 true WO2008093688A1 (ja) 2008-08-07

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PCT/JP2008/051333 Ceased WO2008093688A1 (ja) 2007-01-30 2008-01-30 キメラFcγレセプター及び該レセプターを用いたADCC活性測定方法

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US (2) US8946385B2 (ja)
EP (1) EP2123754B1 (ja)
JP (1) JP5299902B2 (ja)
AT (1) ATE504647T1 (ja)
DE (1) DE602008006041D1 (ja)
WO (1) WO2008093688A1 (ja)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010074049A1 (ja) 2008-12-22 2010-07-01 株式会社 未来創薬研究所 抗hs6st2抗体及びその用途
WO2010074192A1 (ja) 2008-12-26 2010-07-01 国立大学法人東京大学 抗lgr7抗体を用いる癌の診断および治療
WO2010073694A1 (ja) 2008-12-25 2010-07-01 国立大学法人東京大学 抗tm4sf20抗体を用いた癌の診断と治療
WO2011093097A1 (ja) 2010-01-29 2011-08-04 株式会社未来創薬研究所 抗dll3抗体
WO2012144208A1 (ja) 2011-04-18 2012-10-26 国立大学法人東京大学 抗itm2a抗体を用いる癌の診断および治療
WO2013147153A1 (ja) 2012-03-29 2013-10-03 株式会社未来創薬研究所 抗lamp5抗体およびその利用

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CA2672581A1 (en) * 2006-12-14 2008-06-19 Forerunner Pharma Research Co., Ltd. Anti-claudin 3 monoclonal antibody and treatment and diagnosis of cancer using the same
ATE504647T1 (de) 2007-01-30 2011-04-15 Forerunner Pharma Res Co Ltd Chimärer fc gamma rezeptor und verfahren zur bestimmung von adcc-aktivität unter verwendung des rezeptors
EP4541818A3 (en) * 2012-05-25 2025-07-23 Cellectis Methods for engineering allogeneic and immunosuppressive resistant t cell for immunotherapy
EP4282419A1 (en) 2012-12-20 2023-11-29 Purdue Research Foundation Chimeric antigen receptor-expressing t cells as anti-cancer therapeutics
AU2015204729A1 (en) * 2014-01-08 2016-07-21 1Globe Biomedical Co., Ltd. Novel synthetic biology-based ADCC technology
RU2700484C2 (ru) * 2014-04-08 2019-09-17 Регенерон Фармасьютикалз, Инк. Не относящиеся к человеку животные, имеющие гуманизированные fc-гамма-рецепторы
CN107709552B (zh) * 2015-06-10 2022-05-13 南克维斯特公司 用于治疗癌症的修饰的nk-92细胞
US12144850B2 (en) 2016-04-08 2024-11-19 Purdue Research Foundation Methods and compositions for car T cell therapy
AU2018219226B2 (en) 2017-02-07 2024-12-19 Seattle Children's Hospital (dba Seattle Children's Research Institute) Phospholipid ether (PLE) CAR T cell tumor targeting (CTCT) agents
ES3010559T3 (en) 2017-02-28 2025-04-03 Endocyte Inc Compositions and methods for car t cell therapy
US11311576B2 (en) 2018-01-22 2022-04-26 Seattle Children's Hospital Methods of use for CAR T cells
WO2019156795A1 (en) 2018-02-06 2019-08-15 Seattle Children's Hospital (dba Seattle Children's Research Institute) Fluorescein-specific cars exhibiting optimal t cell function against fl-ple labelled tumors
CA3091674A1 (en) 2018-02-23 2019-08-29 Endocyte, Inc. Sequencing method for car t cell therapy
JP7339325B2 (ja) * 2018-03-20 2023-09-05 ナショナル ヘルス リサーチ インスティテューツ 単離抗体、医薬組成物、単離抗体結合体、ダイマー化阻害方法、シグナル伝達阻害方法、管新生阻害方法、治療方法、および断片検出方法
WO2019190990A1 (en) 2018-03-26 2019-10-03 Regeneron Pharmaceuticals, Inc. Humanized rodents for testing therapeutic agents
KR20220163940A (ko) 2020-02-04 2022-12-12 시애틀 칠드런즈 호스피탈 디/비/에이 시애틀 칠드런즈 리서치 인스티튜트 항-디니트로페놀 키메라 항원 수용체
TW202237827A (zh) 2020-12-03 2022-10-01 美商世紀治療股份有限公司 經基因工程改造之細胞及其用途
US11661459B2 (en) 2020-12-03 2023-05-30 Century Therapeutics, Inc. Artificial cell death polypeptide for chimeric antigen receptor and uses thereof
JP2024500847A (ja) 2020-12-18 2024-01-10 センチュリー セラピューティクス,インコーポレイテッド 適合可能な受容体特異性を有するキメラ抗原受容体システム
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010074049A1 (ja) 2008-12-22 2010-07-01 株式会社 未来創薬研究所 抗hs6st2抗体及びその用途
WO2010073694A1 (ja) 2008-12-25 2010-07-01 国立大学法人東京大学 抗tm4sf20抗体を用いた癌の診断と治療
WO2010074192A1 (ja) 2008-12-26 2010-07-01 国立大学法人東京大学 抗lgr7抗体を用いる癌の診断および治療
WO2011093097A1 (ja) 2010-01-29 2011-08-04 株式会社未来創薬研究所 抗dll3抗体
EP3342786A1 (en) 2010-01-29 2018-07-04 Chugai Seiyaku Kabushiki Kaisha Anti-dll3 antibody
EP3907242A1 (en) 2010-01-29 2021-11-10 Chugai Seiyaku Kabushiki Kaisha Anti-dll3 antibody
WO2012144208A1 (ja) 2011-04-18 2012-10-26 国立大学法人東京大学 抗itm2a抗体を用いる癌の診断および治療
WO2013147153A1 (ja) 2012-03-29 2013-10-03 株式会社未来創薬研究所 抗lamp5抗体およびその利用

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EP2123754A1 (en) 2009-11-25
US9733245B2 (en) 2017-08-15
EP2123754A4 (en) 2010-01-27
US20100035280A1 (en) 2010-02-11
JPWO2008093688A1 (ja) 2010-05-20
DE602008006041D1 (de) 2011-05-19
US8946385B2 (en) 2015-02-03
EP2123754B1 (en) 2011-04-06
ATE504647T1 (de) 2011-04-15
US20150079610A1 (en) 2015-03-19
JP5299902B2 (ja) 2013-09-25

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