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Cited 9 time in webofscience Cited 10 time in scopus
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dc.contributor.authorLin, GHY-
dc.contributor.authorStone, JC-
dc.contributor.authorSurh, CD-
dc.contributor.authorWatts, TH-
dc.date.accessioned2016-03-31T08:11:42Z-
dc.date.available2016-03-31T08:11:42Z-
dc.date.created2014-03-07-
dc.date.issued2012-08-
dc.identifier.issn1440-1711-
dc.identifier.other2012-OAK-0000029343-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/14769-
dc.description.abstractImmune complexes combining IL-2 with particular anti-IL-2 antibodies can be used to selectively expand regulatory T cells or memory T cells. Combining IL-2 with anti-IL-2 (Clone S4B6) greatly enhances the biological potency of IL-2 in vivo leading to selective expansion of CD8 memory T cells and NK cells compared with regulatory T cells. Here we show that in vivo administration of IL-2/anti-IL-2 mAb (IL-2/mAb) complexes induces 4-1BB expression on both adoptively transferred antigenspecific memory CD8 T cells as well as on endogenous memory phenotype cells. Remarkably, the accumulation of adoptively transferred memory CD8 T cells following in vivo IL-2/mAb-complex treatment was found to be dependent in part on the presence of 4-1BBL in the host. These effects were independent of IL-2-induced cell division, suggesting that 4-1BBL-induced survival signals contribute to IL-2/mAb-complex-induced T-cell accumulation in vivo. Immunology and Cell Biology (2012) 90, 743-747; doi:10.1038/icb.2011.83; published online 27 September 2011-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherNature Publishing Group-
dc.relation.isPartOfImmunology and Cell Biology-
dc.subjectIL-2-antibody complex-
dc.subjecttherapy-
dc.subject4-1BBL-
dc.subjectCD137-
dc.subjectT cell-
dc.subjectSELECTIVE STIMULATION-
dc.subjectIMMUNE-COMPLEXES-
dc.subjectBIM MODULATION-
dc.subjectIL-2 RECEPTOR-
dc.subjectCUTTING EDGE-
dc.subjectGAMMA-CHAIN-
dc.subjectSURVIVAL-
dc.subjectIMMUNOTHERAPY-
dc.subjectCOSTIMULATION-
dc.subjectLYMPHOCYTES-
dc.titleIn vivo accumulation of T cells in response to IL-2/anti-IL-2 mAb complexes is dependent in part on the TNF family ligand 4-1BBL-
dc.typeArticle-
dc.contributor.college융합생명공학부-
dc.identifier.doi10.1038/ICB.2011.83-
dc.author.googleLin, GHY-
dc.author.googleStone, JC-
dc.author.googleSurh, CD-
dc.author.googleWatts, TH-
dc.relation.volume90-
dc.relation.issue7-
dc.relation.startpage743-
dc.relation.lastpage747-
dc.contributor.id10201353-
dc.relation.journalImmunology and Cell Biology-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationImmunology and Cell Biology, v.90, no.7, pp.743 - 747-
dc.identifier.wosid000307611700010-
dc.date.tcdate2019-01-01-
dc.citation.endPage747-
dc.citation.number7-
dc.citation.startPage743-
dc.citation.titleImmunology and Cell Biology-
dc.citation.volume90-
dc.contributor.affiliatedAuthorSurh, CD-
dc.identifier.scopusid2-s2.0-84864837836-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc4-
dc.description.scptc5*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusSELECTIVE STIMULATION-
dc.subject.keywordPlusBIM MODULATION-
dc.subject.keywordPlusCUTTING EDGE-
dc.subject.keywordPlusGAMMA-CHAIN-
dc.subject.keywordPlusIL-2-
dc.subject.keywordPlusIMMUNE-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusCOSTIMULATION-
dc.subject.keywordPlusLYMPHOCYTES-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorIL-2-antibody complex-
dc.subject.keywordAuthortherapy-
dc.subject.keywordAuthor4-1BBL-
dc.subject.keywordAuthorCD137-
dc.subject.keywordAuthorT cell-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaImmunology-

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