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Cited 157 time in webofscience Cited 157 time in scopus
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dc.contributor.authorLetourneau, S-
dc.contributor.authorvan Leeuwen, EMM-
dc.contributor.authorKrieg, C-
dc.contributor.authorMartin, C-
dc.contributor.authorPantaleo, G-
dc.contributor.authorSprent, J-
dc.contributor.authorSurh, CD-
dc.contributor.authorBoyman, O-
dc.date.accessioned2016-03-31T08:11:35Z-
dc.date.available2016-03-31T08:11:35Z-
dc.date.created2014-03-07-
dc.date.issued2010-02-02-
dc.identifier.issn0027-8424-
dc.identifier.other2010-OAK-0000029348-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/14765-
dc.description.abstractIL-2 is crucial to T cell homeostasis, especially of CD4(+) T regulatory cells and memory CD8(+) cells, as evidenced by vigorous proliferation of these cells in vivo following injections of superagonist IL-2/anti-IL-2 antibody complexes. The mechanism of IL-2/anti-IL-2 antibody complexes is unknown owing to a lack of understanding of IL-2 homeostasis. We show that IL-2 receptor alpha (CD25) plays a crucial role in IL-2 homeostasis. Thus, prolongation of IL-2 half-life and blocking of CD25 using antibodies or CD25-deficient mice led in combination, but not alone, to vigorous IL-2-mediated T cell proliferation, similar to IL-2/anti-IL-2 antibody complexes. These data suggest an unpredicted role for CD25 in IL-2 homeostasis.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherNational Academy of Sciences-
dc.relation.isPartOfNational Academy of Sciences. Proceedings-
dc.subjectCD25-
dc.subjectcytokine-
dc.subjectcytokine/mAb complexes-
dc.subjectT cell homeostasis-
dc.subjectFc receptor-
dc.subjectREGULATORY T-CELLS-
dc.subjectIN-VIVO-
dc.subjectIMMUNE-COMPLEXES-
dc.subjectCUTTING EDGE-
dc.subjectAUTOIMMUNE-DISEASE-
dc.subjectHEPARAN-SULFATE-
dc.subjectDEFICIENT MICE-
dc.subjectFUSION PROTEIN-
dc.subjectBETA-CHAIN-
dc.subjectINTERLEUKIN-2-
dc.titleIL-2/anti-IL-2 antibody complexes show strong biological activity by avoiding interaction with IL-2 receptor alpha subunit CD25.-
dc.typeArticle-
dc.contributor.college융합생명공학부-
dc.identifier.doi10.1073/PNAS.0909384107-
dc.author.googleLetourneau, S-
dc.author.googlevan Leeuwen, EMM-
dc.author.googleKrieg, C-
dc.author.googleMartin, C-
dc.author.googlePantaleo, G-
dc.author.googleSprent, J-
dc.author.googleSurh, CD-
dc.author.googleBoyman, O-
dc.relation.volume107-
dc.relation.issue5-
dc.relation.startpage1271-
dc.relation.lastpage1276-
dc.contributor.id10201353-
dc.relation.journalNational Academy of Sciences. Proceedings-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationNational Academy of Sciences. Proceedings, v.107, no.5, pp.1271 - 1276-
dc.identifier.wosid000274296300067-
dc.date.tcdate2019-01-01-
dc.citation.endPage1276-
dc.citation.number5-
dc.citation.startPage1271-
dc.citation.titleNational Academy of Sciences. Proceedings-
dc.citation.volume107-
dc.contributor.affiliatedAuthorSurh, CD-
dc.identifier.scopusid2-s2.0-76649145452-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc92-
dc.description.scptc79*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusCD8(+) T-CELLS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusCUTTING EDGE-
dc.subject.keywordPlusIMMUNE-COMPLEXES-
dc.subject.keywordPlusHEPARAN-SULFATE-
dc.subject.keywordPlusDEFICIENT MICE-
dc.subject.keywordPlusFUSION PROTEIN-
dc.subject.keywordPlusBETA-CHAIN-
dc.subject.keywordPlusINTERLEUKIN-2-
dc.subject.keywordPlusHOMEOSTASIS-
dc.subject.keywordAuthorCD25-
dc.subject.keywordAuthorcytokine-
dc.subject.keywordAuthorcytokine/mAb complexes-
dc.subject.keywordAuthorT cell homeostasis-
dc.subject.keywordAuthorFc receptor-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-

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