An Anti-B Cell Maturation Antigen Bispecific Antibody for Multiple Myeloma

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dc.contributor.authorRamadoss, Nitya S.ko
dc.contributor.authorSchulman, Andrew D.ko
dc.contributor.authorChoi, Sei-hyunko
dc.contributor.authorRodgers, David T.ko
dc.contributor.authorKazane, Stephanie A.ko
dc.contributor.authorKim, Chan Hyukko
dc.contributor.authorLawson, Brian R.ko
dc.contributor.authorYoung, Travis S.ko
dc.date.accessioned2016-07-04T06:01:47Z-
dc.date.available2016-07-04T06:01:47Z-
dc.date.created2016-05-14-
dc.date.created2016-05-14-
dc.date.created2016-05-14-
dc.date.issued2015-04-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.137, no.16, pp.5288 - 5291-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/209124-
dc.description.abstractThe development of immunotherapies for multiple. myeloma is critical to provide new treatment Strategies to combat drug resistance. We report a bispecific antibody against B cell maturation antigen (BiFab-BCMA), which potently and specifically redirects 1 cells to lyse malignant multiple myeloma cells. BiFab-BCMA lysed target BCMA-positive cell lilies up to more potently than a CS1-targeting bispecific Antibody (BiFab-CS1) developed in an analogous fashion, Further, BiFab-BCMA robustly activated T cells in vitro and mediated rapid tumor regression in an orthotopic:xenograft model of multiple myeloma.. The in vitro :and in vivo activities of BiPab-BCMA are comparable to those of anti-BCMA chimeric antigen receptor T cell therapy CAR-T-BCMA), for which two clinical trials have recently:been initiated. A BCMA-targeted bispecific antibody presents a promising treatment option for multiple myeloma.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectSINGLE-CHAIN ANTIBODY-
dc.subjectIN-VIVO-
dc.subjectMONOCLONAL-ANTIBODY-
dc.subjectPLASMA-CELLS-
dc.subjectIMMUNOTHERAPY-
dc.subjectTHERAPY-
dc.subjectTARGET-
dc.subjectCYTOTOXICITY-
dc.subjectRECEPTOR-
dc.subjectFUTURE-
dc.titleAn Anti-B Cell Maturation Antigen Bispecific Antibody for Multiple Myeloma-
dc.typeArticle-
dc.identifier.wosid000353931500012-
dc.identifier.scopusid2-s2.0-84928749842-
dc.type.rimsART-
dc.citation.volume137-
dc.citation.issue16-
dc.citation.beginningpage5288-
dc.citation.endingpage5291-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.identifier.doi10.1021/jacs.5b01876-
dc.contributor.localauthorKim, Chan Hyuk-
dc.contributor.nonIdAuthorRamadoss, Nitya S.-
dc.contributor.nonIdAuthorSchulman, Andrew D.-
dc.contributor.nonIdAuthorChoi, Sei-hyun-
dc.contributor.nonIdAuthorRodgers, David T.-
dc.contributor.nonIdAuthorKazane, Stephanie A.-
dc.contributor.nonIdAuthorLawson, Brian R.-
dc.contributor.nonIdAuthorYoung, Travis S.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusSINGLE-CHAIN ANTIBODY-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusMONOCLONAL-ANTIBODY-
dc.subject.keywordPlusPLASMA-CELLS-
dc.subject.keywordPlusIMMUNOTHERAPY-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusTARGET-
dc.subject.keywordPlusCYTOTOXICITY-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusFUTURE-
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