FI121012B - Läkemedel innehållande T-lymfocyter för återriktning av cellulär immunitet med protein-tyrosinkinaskimerer - Google Patents
Läkemedel innehållande T-lymfocyter för återriktning av cellulär immunitet med protein-tyrosinkinaskimerer Download PDFInfo
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- FI121012B FI121012B FI973466A FI973466A FI121012B FI 121012 B FI121012 B FI 121012B FI 973466 A FI973466 A FI 973466A FI 973466 A FI973466 A FI 973466A FI 121012 B FI121012 B FI 121012B
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Claims (32)
1. Användning av T-lymfocyter, av vilka varje T-lyrafocyt expresserar ätminstone tvä till membranet bundna 5 kimeriska proteinreceptorer, av vilka nämnda receptorer den första omfattar (a) en första intracellular del av proteintyrosinkinas, som har en förmäga att ge en signal till nämnda T-lymfocyt att förstöra den som objekt varande cellen eller det infektionsframkallande objektet som är 10 bundet till receptorn, och (b) en extracellular del, som har en förmäga att kanna igen och specifikt binda nämnda som objekt varande cell eller infektionsframkallande objekt; och av vilka nämnda receptorer den andra omfattar (a) en extracellulär del, som har en förmäga att känna 15 igen och specifikt binda till nämnda objekt varande cell eller infektionframkallande objekt, och (b) en frän CD28 deriverad intracellulär del, varvid nämnda T-lymfocyter förmär känna igen och förstöra specifikt nämnda som objekt varande cell eller infektionframkallande objekt, i fram-20 ställningen av ett läkemedel för att dirigera en cellim-munrespons i ett däggdjur.
2. Användning enligt patentkrav 2, känneteck-nad av att nämnda som objekt varande cell är av en infektionsf ramkallare infekterad värdcell, en tumor- eller can- 25 cercell eller en cell som bildats genom en autoimmunmeka-nism.
3. Användning enligt patentkrav 1, känneteck-n a d av att nämnda proteintyrosinkinas är en medlem av Syk-kinasgruppen.
4. Användning enligt patentkrav 3, känneteck- nad av att nämnda proteintyrosinkinas är Syk.
5. Användning enligt patentkrav 4, känneteck-n a d av att nämnda intracellulära del innehäller aminosy-rorna 336 - 628 av svinets Syk eller aminosyrorna 338 - 630 35 av människans Syk.
6. Användning enligt patentkrav 1, känneteck-nad av att nämnda T-lymfocyt expresserar en tredje till membranet bunden kimerisk proteinreceptor, vilken nämnda tredje kimeriska receptor omfattar (a) en andra intracel- 5 lulär del av proteintyrosinkinas, som förmär ge en signal till nämnda T-lymfocyt att förstöra den som objekt varande cellen eller det infektionsframkallande objekt som är bun-det till receptorn, och (b) en extracellulär del, som förmär känna igen och specifikt binda den som objekt varande 10 cellen eller det infektionsframkallande objektet.
7. Användning enligt patentkrav 6, känneteck-nad av att den ena av nämnda proteintyrosinkinaser är en medlem av Syk-kinasgruppen och den andra av nämnda proteintyrosinkinaser är en medlem av Src-kinasgruppen.
8. Användning enligt patentkrav 6, känneteck- n a d av att den ena av nämnda proteintyrosinkinaser är ZAP-70 och den andra av nämnda proteintyrosinkinaser är Fyn.
9. Användning enligt patentkrav 6, känneteck-20 n a d av att den ena av nämnda proteintyrosinkinaser är ZAP-70 och den andra av nämnda proteintyrosinkinaser är Lck.
10. Användning enligt patentkrav 8 eller 9, kännetecknad av att nämnda ZAP-7 0 del innehäller män- 25 niskans Tyr 369 av ZAP-70.
11. Användning enligt patentkrav 1 eller 6, kännetecknad av att nämnda immunrespons är oberoende av MHC.
12. Användning enligt patentkrav 1 eller 6, 30 kännetecknad av att nämnda T-lymfocyter är cytotoxis- ka T-lymfocyter.
13. Användning enligt patentkrav 1, kännetecknad av att som nämnda infektionsframkallande objekt är ett immunbristvirus .
14. Änvändning enligt patentkrav 13, känne-tecknad av att nämnda extracellulära del omfattar tili HIV-manteln bindande del av CD4. 15. Änvändning enligt patentkrav 1, k anne-5 tecknad av att nämnda T-lymfocyter förstör nämnda som objekt varande cell eller infektionsframkallande objekt genom cytolys.
15 Fyn.
16. T-lymfocyt, kännetecknad av att den ex-presserar ätminstone tvä tili membranet bundna kimeriska 10 proteinreeeptorer, av vilka nämnda reeeptorer den första omfattar (a) en första intracellulär del av proteintyro-sinkinas, som har en förmäga att ge en signal till nämnda T-lymfocyt att förstöra den som objekt varande cellen eller det infektionsframkallande objektet som är bundet tili 15 reeeptorn, och (b) en extracellulär del, som har en förmäga att känna igen och specifikt binda nämnda som objekt varande cell eller infektionsframkallande objekt; och av vilka nämnda reeeptorer den andra omfattar (a) en extracellulär del, som har en förmäga att känna igen och speci-20 fikt binda tili nämnda objekt varande cell eller infektionsf ramkallande objekt, och (b) en frän CD28 deriverad intracellulär del, varvid nämnda T-lymfocyt förmär känna igen och förstöra specifikt nämnda som objekt varande cell eller infektionsframkallande objekt.
17. Cell enligt patentkrav 16, kännetecknad av att nämnda proteintyrosinkinas är en medlem av Syk-kinasgruppen.
18. T-lymfocyt enligt patentkrav 17, känne tecknad av att nämnda proteintyrosinkinas är Syk. 30
19. T-lymfocyt enligt patentkrav 18, känne tecknad av att nämnda intracellulära del innehäller aminosyrorna 336 - 628 av svinets Syk eller aminosyrorna 338 - 630 av människans Syk.
20. T-lymfocyt enligt patentkrav 16, känne- 35 tecknad av att nämnda T-lymfocyt expresserar en tredje tili membranet bunden kimerisk proteinreeeptor, vilken nämnda tredje kimeriska receptor omfattar (a) en andra in-tracellulär del av proteintyrosinkinas, sora förmär ge en signal till nämnda T-lymfocyt att förstöra den som objekt varande cellen eller det infektionsframkallande objekt som 5 är bundet tili receptorn, och (b) en extracellular del, som förmär känna igen och specifikt binda den som objekt varande cellen eller det infektionsframkallande objektet.
21. T-lymfocyt enligt patentkrav 20, känne- tecknad av att den ena av nämnda proteintyrosinkinaser 10 är en medlem av Syk-kinasgruppen och den andra av nämnda proteintyrosinkinaser är en medlem av Src-kinasgruppen.
22. T-lymfocyt enligt patentkrav 20, känne- tecknad av att den ena av nämnda proteintyrosinkinaser är ZAP-70 och den andra av nämnda proteintyrosinkinaser är
23. T-lymfocyt enligt patentkrav 20, känne- tecknad av att den ena av nämnda proteintyrosinkinaser är ZAP-70 och den andra av nämnda proteintyrosinkinaser är Lck. 20
24. T-lymfocyt enligt patentkrav 22 eller 23, kännetecknad av att nämnda ZAP-7 0 del innehäller män-niskans Tyr 369 av ZAP-70.
25. T-lymfocyt enligt patentkrav 16 eller 20, kännetecknad av att nämnda t-lymfocyter är cytotoxis- 25 ka T-lymfocyter.
26. T-lymfocyt enligt patentkrav 16, känne tecknad av att nämnda infektionsframkallande objekt är ett immunbristvirus.
27. T-lymfocyt enligt patentkrav 26, känne- 30 tecknad av att nämnda extracellulära del omfattar den tili HIV-manteln bindande del av CD4.
28. T-lymfocyt enligt patentkrav 16, känne tecknad av att nämnda T-lymfocyter förstör nämnda som objekt varande cell eller infektionsframkallande objekt 35 genom cytolys.
29. T-lymfocyt enligt patentkrav 16 eller 20, kännetecknad av att nämnda bindning är oberoende av MHC.
30. T-lymfocyt enligt patentkrav 16 eller 20, 5 kännetecknad av att nämnda extracellulära del omfattar en del som binder till receptorns ligand, den del av liganden som binds till receptorn, till antikroppens antigen bindande del eller ett funktionellt derivat av dessa.
31. DNA, kännetecknatav att det kodar 10 ett till membranet bundet kimeriskt proteinreceptorpar, varvid den första av nämnda receptorer omfattar (a) en första intracellular del av proteintyrosinkinas, som har en förmäga att ge en signal till nämnda T-lymfocyt att förstöra den som objekt varande cellen eller det infek-15 tionsframkallande objektet som är bundet till receptorn, och (b) en extracellular del, som har en förmäga att känna igen och specifikt binda nämnda som objekt varande cell eller infektionsframkallande objekt; och av vilka nämnda receptorer den andra omfattar (a) en extracellulär del, 20 som har en förmäga att känna igen och specifikt binda till nämnda objekt varande cell eller infektionframkallande objekt, och (b) en frän CD28 deriverad intracellulär del, varvid nämnda T-lymfocyter förmär känna igen och förstöra specifikt nämnda som objekt varande cell eller infektion-25 framkallande objekt.
32. Vektor, kännetecknad av att den omfattar ett DNA enligt patentkrav 31 som kodar till membranet bindande kimeriskt proteinreceptorpar.
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US08/394,177 US5912170A (en) | 1991-03-07 | 1995-02-24 | Redirection of cellular immunity by protein-tyrosine kinase chimeras |
PCT/US1996/001001 WO1996026265A1 (en) | 1995-02-24 | 1996-01-24 | Redirection of cellular immunity by protein-tyrosine kinase chimeras |
US9601001 | 1996-01-24 |
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Families Citing this family (97)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5912170A (en) * | 1991-03-07 | 1999-06-15 | The General Hospital Corporation | Redirection of cellular immunity by protein-tyrosine kinase chimeras |
US5851828A (en) | 1991-03-07 | 1998-12-22 | The General Hospital Corporation | Targeted cytolysis of HIV-infected cells by chimeric CD4 receptor-bearing cells |
US6753162B1 (en) | 1991-03-07 | 2004-06-22 | The General Hospital Corporation | Targeted cytolysis of HIV-infected cells by chimeric CD4 receptor-bearing cells |
US6004811A (en) | 1991-03-07 | 1999-12-21 | The Massachussetts General Hospital | Redirection of cellular immunity by protein tyrosine kinase chimeras |
US7049136B2 (en) | 1991-03-07 | 2006-05-23 | The General Hospital Corporation | Redirection of cellular immunity by receptor chimeras |
DK0871495T3 (da) * | 1995-02-24 | 2005-10-17 | Gen Hospital Corp | Omdirigering af cellulær immunitet med receptorkimærer |
GB9526131D0 (en) * | 1995-12-21 | 1996-02-21 | Celltech Therapeutics Ltd | Recombinant chimeric receptors |
IL137419A0 (en) * | 2000-07-20 | 2001-07-24 | Yissum Res Dev Co | Nk cells activating receptors and their therapeutic and diagnostic uses |
WO2005068616A2 (en) * | 2004-01-16 | 2005-07-28 | Fraunhofer Gesellschaft zur Förderung der angewandten Forschung e.V. | Immunokinases |
IL296832A (en) | 2005-10-18 | 2022-11-01 | Nat Jewish Health | A process for making red blood cells using immortal hematopoietic stem cells and erythropoietin |
EP1800695A1 (en) * | 2005-12-21 | 2007-06-27 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Immuno-RNA-constructs |
ES2657480T3 (es) | 2006-08-11 | 2018-03-05 | Life Sciences Research Partners Vzw | Péptidos inmunogénicos y su uso en trastornos inmunitarios |
EP2171456A2 (en) * | 2007-07-25 | 2010-04-07 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Self coupling recombinant antibody fusion proteins |
WO2009035600A2 (en) * | 2007-09-11 | 2009-03-19 | University Of Maryland, Baltimore | Zap-70 as predictor and modulator of effector function of t cells |
EA021131B1 (ru) | 2008-05-16 | 2015-04-30 | Тэйга Байотекнолоджис, Инк. | Антитела и способы их получения |
IL301475A (en) | 2008-08-28 | 2023-05-01 | Taiga Biotechnologies Inc | Laboratory methods for increasing the vitality of the cells of the immune system |
WO2011119920A2 (en) | 2010-03-25 | 2011-09-29 | Oregon Health & Science University | Cmv glycoproteins and recombinant vectors |
HUE037408T2 (hu) | 2011-06-10 | 2018-08-28 | Univ Oregon Health & Science | CMV glikoproteinek és rekombináns vektorok |
US20130189754A1 (en) | 2011-09-12 | 2013-07-25 | International Aids Vaccine Initiative | Immunoselection of recombinant vesicular stomatitis virus expressing hiv-1 proteins by broadly neutralizing antibodies |
EP2586461A1 (en) | 2011-10-27 | 2013-05-01 | Christopher L. Parks | Viral particles derived from an enveloped virus |
GB201201511D0 (en) | 2012-01-30 | 2012-03-14 | Univ Leuven Kath | Modified epitopes for boosting CD4+ T-cell responses |
ES2631608T3 (es) | 2012-06-27 | 2017-09-01 | International Aids Vaccine Initiative | Variante de la glicoproteína Env del VIH-1 |
US9789135B2 (en) | 2012-07-20 | 2017-10-17 | Taiga Biotechnologies, Inc. | Enhanced reconstitution and autoreconstitution of the hematopoietic compartment |
US10272115B2 (en) | 2013-03-11 | 2019-04-30 | Taiga Biotechnologies, Inc. | Production and use of red blood cells |
EP2848937A1 (en) | 2013-09-05 | 2015-03-18 | International Aids Vaccine Initiative | Methods of identifying novel HIV-1 immunogens |
US10058604B2 (en) | 2013-10-07 | 2018-08-28 | International Aids Vaccine Initiative | Soluble HIV-1 envelope glycoprotein trimers |
WO2015077717A1 (en) | 2013-11-25 | 2015-05-28 | The Broad Institute Inc. | Compositions and methods for diagnosing, evaluating and treating cancer by means of the dna methylation status |
US11725237B2 (en) | 2013-12-05 | 2023-08-15 | The Broad Institute Inc. | Polymorphic gene typing and somatic change detection using sequencing data |
AU2014368898B2 (en) | 2013-12-20 | 2020-06-11 | Dana-Farber Cancer Institute, Inc. | Combination therapy with neoantigen vaccine |
EP2990416B1 (en) | 2014-08-29 | 2018-06-20 | GEMoaB Monoclonals GmbH | Universal chimeric antigen receptor expressing immune cells for targeting of diverse multiple antigens and method of manufacturing the same and use of the same for treatment of cancer, infections and autoimmune disorders |
US10993997B2 (en) | 2014-12-19 | 2021-05-04 | The Broad Institute, Inc. | Methods for profiling the t cell repertoire |
WO2016100975A1 (en) | 2014-12-19 | 2016-06-23 | Massachsetts Institute Ot Technology | Molecular biomarkers for cancer immunotherapy |
US10174292B2 (en) | 2015-03-20 | 2019-01-08 | International Aids Vaccine Initiative | Soluble HIV-1 envelope glycoprotein trimers |
US9931394B2 (en) | 2015-03-23 | 2018-04-03 | International Aids Vaccine Initiative | Soluble HIV-1 envelope glycoprotein trimers |
EP3297660A2 (en) | 2015-05-20 | 2018-03-28 | The Broad Institute Inc. | Shared neoantigens |
WO2016205749A1 (en) | 2015-06-18 | 2016-12-22 | The Broad Institute Inc. | Novel crispr enzymes and systems |
US20190255107A1 (en) | 2015-10-09 | 2019-08-22 | The Brigham And Women's Hospital, Inc. | Modulation of novel immune checkpoint targets |
WO2017075451A1 (en) | 2015-10-28 | 2017-05-04 | The Broad Institute Inc. | Compositions and methods for evaluating and modulating immune responses by detecting and targeting pou2af1 |
EP3368689B1 (en) | 2015-10-28 | 2020-06-17 | The Broad Institute, Inc. | Composition for modulating immune responses by use of immune cell gene signature |
WO2017075465A1 (en) | 2015-10-28 | 2017-05-04 | The Broad Institute Inc. | Compositions and methods for evaluating and modulating immune responses by detecting and targeting gata3 |
CA3005878A1 (en) | 2015-11-19 | 2017-05-26 | The Brigham And Women's Hospital, Inc. | Lymphocyte antigen cd5-like (cd5l)-interleukin 12b (p40) heterodimers in immunity |
WO2017184590A1 (en) | 2016-04-18 | 2017-10-26 | The Broad Institute Inc. | Improved hla epitope prediction |
WO2018035364A1 (en) | 2016-08-17 | 2018-02-22 | The Broad Institute Inc. | Product and methods useful for modulating and evaluating immune responses |
WO2018049025A2 (en) | 2016-09-07 | 2018-03-15 | The Broad Institute Inc. | Compositions and methods for evaluating and modulating immune responses |
WO2018067991A1 (en) | 2016-10-07 | 2018-04-12 | The Brigham And Women's Hospital, Inc. | Modulation of novel immune checkpoint targets |
US10583156B2 (en) | 2016-12-02 | 2020-03-10 | Taiga Biotechnologies, Inc. | Nanoparticle formulations |
US11549149B2 (en) | 2017-01-24 | 2023-01-10 | The Broad Institute, Inc. | Compositions and methods for detecting a mutant variant of a polynucleotide |
EP3579870A4 (en) | 2017-02-07 | 2020-12-30 | Seattle Children's Hospital (DBA Seattle Children's Research Institute) | PHOSPHOLIPID ETHER (PLE) T CAR-LYMPHOCYTE TUMOR (CTCT) TARGETING AGENTS |
CA3053133A1 (en) | 2017-02-12 | 2018-08-16 | Neon Therapeutics, Inc. | Hla-based methods and compositions and uses thereof |
JP7178355B2 (ja) | 2017-02-28 | 2022-11-25 | エンドサイト・インコーポレイテッド | Car t細胞療法のための組成物および方法 |
WO2018183908A1 (en) | 2017-03-31 | 2018-10-04 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for treating ovarian tumors |
EP3606518A4 (en) | 2017-04-01 | 2021-04-07 | The Broad Institute, Inc. | METHODS AND COMPOSITIONS FOR DETECTION AND MODULATION OF IMMUNOTHERAPY RESISTANCE GENE SIGNATURE IN CANCER |
US20200071773A1 (en) | 2017-04-12 | 2020-03-05 | Massachusetts Eye And Ear Infirmary | Tumor signature for metastasis, compositions of matter methods of use thereof |
WO2018195019A1 (en) | 2017-04-18 | 2018-10-25 | The Broad Institute Inc. | Compositions for detecting secretion and methods of use |
WO2018195339A1 (en) | 2017-04-19 | 2018-10-25 | Board Of Regents, The University Of Texas System | Immune cells expressing engineered antigen receptors |
WO2018232195A1 (en) | 2017-06-14 | 2018-12-20 | The Broad Institute, Inc. | Compositions and methods targeting complement component 3 for inhibiting tumor growth |
WO2019014581A1 (en) | 2017-07-14 | 2019-01-17 | The Broad Institute, Inc. | METHODS AND COMPOSITIONS FOR MODULATING THE ACTIVITY OF A CYTOTOXIC LYMPHOCYTE |
EP4026554A1 (en) | 2017-08-03 | 2022-07-13 | Taiga Biotechnologies, Inc. | Methods and compositions for the treatment of melanoma |
US10149898B2 (en) | 2017-08-03 | 2018-12-11 | Taiga Biotechnologies, Inc. | Methods and compositions for the treatment of melanoma |
EP3684397A4 (en) | 2017-09-21 | 2021-08-18 | The Broad Institute, Inc. | SYSTEMS, METHODS AND COMPOSITIONS FOR TARGETED EDITION OF NUCLEIC ACIDS |
WO2019070755A1 (en) | 2017-10-02 | 2019-04-11 | The Broad Institute, Inc. | METHODS AND COMPOSITIONS FOR DETECTING AND MODULATING A GENETIC SIGNATURE OF IMMUNOTHERAPY RESISTANCE IN CANCER |
WO2019084055A1 (en) | 2017-10-23 | 2019-05-02 | Massachusetts Institute Of Technology | CLASSIFICATION OF GENETIC VARIATION FROM UNICELLULAR TRANSCRIPTOMS |
EP3710039A4 (en) | 2017-11-13 | 2021-08-04 | The Broad Institute, Inc. | METHODS AND COMPOSITIONS FOR CANCER TREATMENT BY TARGETING THE CLEC2D-KLRB1 PATH |
US11994512B2 (en) | 2018-01-04 | 2024-05-28 | Massachusetts Institute Of Technology | Single-cell genomic methods to generate ex vivo cell systems that recapitulate in vivo biology with improved fidelity |
US11311576B2 (en) | 2018-01-22 | 2022-04-26 | Seattle Children's Hospital | Methods of use for CAR T cells |
CA3093078A1 (en) | 2018-03-06 | 2019-09-12 | The Trustees Of The University Of Pennsylvania | Prostate-specific membrane antigen cars and methods of use thereof |
US11957695B2 (en) | 2018-04-26 | 2024-04-16 | The Broad Institute, Inc. | Methods and compositions targeting glucocorticoid signaling for modulating immune responses |
US20210371932A1 (en) | 2018-06-01 | 2021-12-02 | Massachusetts Institute Of Technology | Methods and compositions for detecting and modulating microenvironment gene signatures from the csf of metastasis patients |
WO2019241273A1 (en) | 2018-06-11 | 2019-12-19 | The Broad Institute, Inc. | Lineage tracing using mitochondrial genome mutations and single cell genomics |
US12036240B2 (en) | 2018-06-14 | 2024-07-16 | The Broad Institute, Inc. | Compositions and methods targeting complement component 3 for inhibiting tumor growth |
WO2020068304A2 (en) | 2018-08-20 | 2020-04-02 | The Broad Institute, Inc. | Inhibitors of rna-guided nuclease target binding and uses thereof |
WO2020041384A1 (en) | 2018-08-20 | 2020-02-27 | The Broad Institute, Inc. | 3-phenyl-2-cyano-azetidine derivatives, inhibitors of rna-guided nuclease activity |
US20210324357A1 (en) | 2018-08-20 | 2021-10-21 | The Brigham And Women's Hospital, Inc. | Degradation domain modifications for spatio-temporal control of rna-guided nucleases |
US20210382068A1 (en) | 2018-10-02 | 2021-12-09 | Dana-Farber Cancer Institute, Inc. | Hla single allele lines |
WO2020081730A2 (en) | 2018-10-16 | 2020-04-23 | Massachusetts Institute Of Technology | Methods and compositions for modulating microenvironment |
US20220170097A1 (en) | 2018-10-29 | 2022-06-02 | The Broad Institute, Inc. | Car t cell transcriptional atlas |
WO2020092057A1 (en) | 2018-10-30 | 2020-05-07 | Yale University | Compositions and methods for rapid and modular generation of chimeric antigen receptor t cells |
WO2020131586A2 (en) | 2018-12-17 | 2020-06-25 | The Broad Institute, Inc. | Methods for identifying neoantigens |
BR112021012278A2 (pt) | 2018-12-21 | 2021-12-14 | Biontech Us Inc | Método e sistema para a preparação de células hla de classe ii-específica de epitopes e de síntese de cd4 + t |
US11739156B2 (en) | 2019-01-06 | 2023-08-29 | The Broad Institute, Inc. Massachusetts Institute of Technology | Methods and compositions for overcoming immunosuppression |
US20220154282A1 (en) | 2019-03-12 | 2022-05-19 | The Broad Institute, Inc. | Detection means, compositions and methods for modulating synovial sarcoma cells |
US20220142948A1 (en) | 2019-03-18 | 2022-05-12 | The Broad Institute, Inc. | Compositions and methods for modulating metabolic regulators of t cell pathogenicity |
WO2020236967A1 (en) | 2019-05-20 | 2020-11-26 | The Broad Institute, Inc. | Random crispr-cas deletion mutant |
WO2020243371A1 (en) | 2019-05-28 | 2020-12-03 | Massachusetts Institute Of Technology | Methods and compositions for modulating immune responses |
US20220282333A1 (en) | 2019-08-13 | 2022-09-08 | The General Hospital Corporation | Methods for predicting outcomes of checkpoint inhibition and treatment thereof |
US20220298501A1 (en) | 2019-08-30 | 2022-09-22 | The Broad Institute, Inc. | Crispr-associated mu transposase systems |
WO2021055372A1 (en) * | 2019-09-16 | 2021-03-25 | Fred Hutchinson Cancer Research Center | Chimeric receptor proteins and uses thereof |
US11981922B2 (en) | 2019-10-03 | 2024-05-14 | Dana-Farber Cancer Institute, Inc. | Methods and compositions for the modulation of cell interactions and signaling in the tumor microenvironment |
US11793787B2 (en) | 2019-10-07 | 2023-10-24 | The Broad Institute, Inc. | Methods and compositions for enhancing anti-tumor immunity by targeting steroidogenesis |
US11844800B2 (en) | 2019-10-30 | 2023-12-19 | Massachusetts Institute Of Technology | Methods and compositions for predicting and preventing relapse of acute lymphoblastic leukemia |
EP4196579A1 (en) | 2020-08-13 | 2023-06-21 | Yale University | Compositions and methods for engineering and selection of car t cells with desired phenotypes |
WO2023173137A1 (en) | 2022-03-11 | 2023-09-14 | Yale University | Compositions and methods for efficient and stable genetic modification of eukaryotic cells |
WO2023220644A1 (en) | 2022-05-10 | 2023-11-16 | Yale University | Compositions and methods of synthetic ctla-4 tails for reprogramming of car-t cells and enhancement of anti-tumor efficacy |
WO2024077256A1 (en) | 2022-10-07 | 2024-04-11 | The General Hospital Corporation | Methods and compositions for high-throughput discovery ofpeptide-mhc targeting binding proteins |
WO2024124044A1 (en) | 2022-12-07 | 2024-06-13 | The Brigham And Women’S Hospital, Inc. | Compositions and methods targeting sat1 for enhancing anti¬ tumor immunity during tumor progression |
WO2024155821A1 (en) | 2023-01-18 | 2024-07-25 | Yale University | Chimeric antigen receptors (car) with intrinsically disordered regions and methods of use thereof |
WO2024192141A1 (en) | 2023-03-13 | 2024-09-19 | Dana-Farber Cancer Institute, Inc. | Treatment of cancers having a drug-resistant mesenchymal cell state |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4873190A (en) * | 1984-06-13 | 1989-10-10 | Massachusetts Institute Of Technology | Heterodimeric T lymphocyte receptor |
GB8422238D0 (en) * | 1984-09-03 | 1984-10-10 | Neuberger M S | Chimeric proteins |
US4690915A (en) * | 1985-08-08 | 1987-09-01 | The United States Of America As Represented By The Department Of Health And Human Services | Adoptive immunotherapy as a treatment modality in humans |
US4946778A (en) * | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
DE3785186T2 (de) * | 1986-09-02 | 1993-07-15 | Enzon Lab Inc | Bindungsmolekuele mit einzelpolypeptidkette. |
US4808151A (en) * | 1987-04-27 | 1989-02-28 | E. I. Du Pont De Nemours And Company | Simplified method for the preparation of human lymphokine activated killer cells |
US5091513A (en) * | 1987-05-21 | 1992-02-25 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
JPS6463394A (en) * | 1987-09-04 | 1989-03-09 | Kyowa Hakko Kogyo Kk | Novel chimera polypeptide |
PT88641B (pt) * | 1987-10-02 | 1993-04-30 | Genentech Inc | Metodo para a preparacao de uma variante de adesao |
US5336603A (en) * | 1987-10-02 | 1994-08-09 | Genentech, Inc. | CD4 adheson variants |
IL86278A (en) * | 1988-05-04 | 2003-06-24 | Yeda Res & Dev | Endowing cells with antibody specificity using chimeric t cell receptor |
CA2000878C (en) * | 1988-10-18 | 1999-06-29 | Jean-Pierre Kinet | Cdnas coding for the subunit of the high-affinity receptor for immunoglobulin e |
US5225538A (en) * | 1989-02-23 | 1993-07-06 | Genentech, Inc. | Lymphocyte homing receptor/immunoglobulin fusion proteins |
FR2644463A1 (sv) * | 1989-03-17 | 1990-09-21 | Pasteur Institut | |
EP0394827A1 (en) * | 1989-04-26 | 1990-10-31 | F. Hoffmann-La Roche Ag | Chimaeric CD4-immunoglobulin polypeptides |
WO1991010736A2 (en) * | 1990-01-19 | 1991-07-25 | Dana Farber Cancer Institute | CLONING AND CHARACTERIZATION OF THE CD3θ SUBUNIT |
DE69123241T2 (de) * | 1990-12-14 | 1997-04-17 | Cell Genesys Inc | Chimärische ketten zur transduktion von rezeptorverbundenen signalwegen |
US5851828A (en) | 1991-03-07 | 1998-12-22 | The General Hospital Corporation | Targeted cytolysis of HIV-infected cells by chimeric CD4 receptor-bearing cells |
IL101147A (en) * | 1991-03-07 | 2004-06-20 | Gen Hospital Corp | Change of direction of cellular immunity by chimera receptors |
US6004811A (en) * | 1991-03-07 | 1999-12-21 | The Massachussetts General Hospital | Redirection of cellular immunity by protein tyrosine kinase chimeras |
US5912170A (en) | 1991-03-07 | 1999-06-15 | The General Hospital Corporation | Redirection of cellular immunity by protein-tyrosine kinase chimeras |
WO1993019163A1 (en) * | 1992-03-18 | 1993-09-30 | Yeda Research And Development Co, Ltd. | Chimeric receptor genes and cells transformed therewith |
ATE236973T1 (de) * | 1993-07-16 | 2003-04-15 | Gen Hospital Corp | Änderung der zellulären immunität durch rezeptorchimäre |
US5439819A (en) * | 1993-08-27 | 1995-08-08 | The Regents Of The University Of California | Chimeric protein tyrosine kinases |
US5712149A (en) * | 1995-02-03 | 1998-01-27 | Cell Genesys, Inc. | Chimeric receptor molecules for delivery of co-stimulatory signals |
JP3782521B2 (ja) | 1996-08-23 | 2006-06-07 | 富士通コンポーネント株式会社 | 押釦構造およびキーボード |
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