An Immunosuppressive Antibody-Drug Conjugate

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dc.contributor.authorWang, Rongsheng E.ko
dc.contributor.authorLiu, Taoko
dc.contributor.authorWang, Yingko
dc.contributor.authorCao, Yuko
dc.contributor.authorDu, Jintangko
dc.contributor.authorLuo, Xiaozhouko
dc.contributor.authorDeshmukh, Vishalko
dc.contributor.authorKim, Chan Hyukko
dc.contributor.authorLawson, Brian R.ko
dc.contributor.authorTremblay, Matthew S.ko
dc.contributor.authorYoung, Travis S.ko
dc.contributor.authorKazane, Stephanie A.ko
dc.contributor.authorWang, Fengko
dc.contributor.authorSchultz, Peter G.ko
dc.date.accessioned2016-07-04T06:01:53Z-
dc.date.available2016-07-04T06:01:53Z-
dc.date.created2016-05-14-
dc.date.created2016-05-14-
dc.date.created2016-05-14-
dc.date.issued2015-03-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.137, no.9, pp.3229 - 3232-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/209125-
dc.description.abstractWe have developed a novel antibody-drug conjugate (ADC) that can selectively deliver the Lck inhibitor dasatinib to human T lymphocytes. This ADC is based on a humanized antibody that selectively binds with high affinity to CXCR4, an antigen that is selectively expressed on hematopoietic cells. The resulting dasatinib-antibody conjugate suppresses T-cell-receptor (TCR)-mediated T-cell activation and cytokine expression with low nM EC50 and has minimal effects on cell viability. This ADC may lead to a new class of selective immunosuppressive drugs with improved safety and extend the ADC strategy to the targeted delivery of kinase inhibitors for indications beyond oncology.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectCHEMOKINE RECEPTOR CXCR4-
dc.subjectSRC/ABL KINASE INHIBITOR-
dc.subjectHUMAN T-LYMPHOCYTES-
dc.subjectIN-VITRO-
dc.subjectRATIONAL DESIGN-
dc.subjectBREAST-CANCER-
dc.subjectCELL-RECEPTOR-
dc.subjectDASATINIB-
dc.subjectACTIVATION-
dc.subjectBMS-354825-
dc.titleAn Immunosuppressive Antibody-Drug Conjugate-
dc.typeArticle-
dc.identifier.wosid000351187200020-
dc.identifier.scopusid2-s2.0-84924690207-
dc.type.rimsART-
dc.citation.volume137-
dc.citation.issue9-
dc.citation.beginningpage3229-
dc.citation.endingpage3232-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.identifier.doi10.1021/jacs.5b00620-
dc.contributor.localauthorKim, Chan Hyuk-
dc.contributor.nonIdAuthorWang, Rongsheng E.-
dc.contributor.nonIdAuthorLiu, Tao-
dc.contributor.nonIdAuthorWang, Ying-
dc.contributor.nonIdAuthorCao, Yu-
dc.contributor.nonIdAuthorDu, Jintang-
dc.contributor.nonIdAuthorLuo, Xiaozhou-
dc.contributor.nonIdAuthorDeshmukh, Vishal-
dc.contributor.nonIdAuthorLawson, Brian R.-
dc.contributor.nonIdAuthorTremblay, Matthew S.-
dc.contributor.nonIdAuthorYoung, Travis S.-
dc.contributor.nonIdAuthorKazane, Stephanie A.-
dc.contributor.nonIdAuthorWang, Feng-
dc.contributor.nonIdAuthorSchultz, Peter G.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCHEMOKINE RECEPTOR CXCR4-
dc.subject.keywordPlusSRC/ABL KINASE INHIBITOR-
dc.subject.keywordPlusHUMAN T-LYMPHOCYTES-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusRATIONAL DESIGN-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusCELL-RECEPTOR-
dc.subject.keywordPlusDASATINIB-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusBMS-354825-
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