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Thymic low affinity/avidity interaction selects natural Th1 cells

DC Field Value Language
dc.contributor.authorKang, Byung Hyun-
dc.contributor.authorPark, Hyo Jin-
dc.contributor.authorYum, Hye In-
dc.contributor.authorPark, Seung Pyo-
dc.contributor.authorPark, Jin Kyun-
dc.contributor.authorKang, Eun Ha-
dc.contributor.authorLee, Jae-Il-
dc.contributor.authorLee, Eun Bong-
dc.contributor.authorPark, Chung-Gyu-
dc.contributor.authorJung, Kyeong Cheon-
dc.contributor.authorPark, Seong Hoe-
dc.date.accessioned2015-12-11T09:02:08Z-
dc.date.available2015-12-11T09:02:08Z-
dc.date.created2018-10-30-
dc.date.issued2015-06-
dc.identifier.citationJournal of Immunology, Vol.194 No.12, pp.5861-5871-
dc.identifier.issn0022-1767-
dc.identifier.urihttps://hdl.handle.net/10371/94804-
dc.description.abstractIdentification of intrathymic eomesodermin(+) (Eomes(+)) CD4 T cells creates a novel idea that there is more than one way for the generation of innate CD4 T cells. Promyelocytic leukemia zinc finger protein(+) T cells and natural Th17 cells are known to be generated by sensing a high and persistent TCR strength, whereas this is not the case for Eomes(+) CD4 T cells. These cells go through low-level signal during the entire maturation pathway, which subsequently leads to induction of high susceptibility to cytokine IL-4. This event seems to be a major determinant for the generation of this type of cell. These T cells are functionally equivalent to Th1 cells that are present in the periphery, and this event takes place both in transgenic and in wild-type mice. There is additional evidence that this type of Eomes(+) innate CD4 T cell is also present in human cord blood.-
dc.language영어-
dc.language.isoen-
dc.publisherAmerican Association of Immunologists-
dc.titleThymic low affinity/avidity interaction selects natural Th1 cells-
dc.typeArticle-
dc.contributor.AlternativeAuthor강병현-
dc.contributor.AlternativeAuthor박효진-
dc.contributor.AlternativeAuthor염혜인-
dc.contributor.AlternativeAuthor박승표-
dc.contributor.AlternativeAuthor박진균-
dc.contributor.AlternativeAuthor강은하-
dc.contributor.AlternativeAuthor이재일-
dc.contributor.AlternativeAuthor이은봉-
dc.contributor.AlternativeAuthor박정규-
dc.contributor.AlternativeAuthor정경천-
dc.contributor.AlternativeAuthor박성회-
dc.identifier.doi10.4049/jimmunol.1401628-
dc.citation.journaltitleJournal of Immunology-
dc.identifier.wosid000355757800032-
dc.identifier.scopusid2-s2.0-84931305583-
dc.description.srndOAIID:oai:osos.snu.ac.kr:snu2015-01/102/0000000922/1-
dc.description.srndADJUST_YN:N-
dc.description.srndEMP_ID:D026822-
dc.description.srndDEPT_CD:801-
dc.description.srndCITE_RATE:4.922-
dc.description.srndDEPT_NM:의학과-
dc.description.srndSCOPUS_YN:Y-
dc.description.srndCONFIRM:Y-
dc.citation.endpage5871-
dc.citation.number12-
dc.citation.startpage5861-
dc.citation.volume194-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorPark, Jin Kyun-
dc.contributor.affiliatedAuthorLee, Jae-Il-
dc.contributor.affiliatedAuthorLee, Eun Bong-
dc.contributor.affiliatedAuthorPark, Chung-Gyu-
dc.contributor.affiliatedAuthorJung, Kyeong Cheon-
dc.contributor.affiliatedAuthorPark, Seong Hoe-
dc.identifier.srnd2015-01/102/0000000922/1-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCD8(+) T-CELLS-
dc.subject.keywordPlusTHYMOCYTE-THYMOCYTE INTERACTION-
dc.subject.keywordPlusPOSITIVE SELECTION-
dc.subject.keywordPlusINNATE-LIKE-
dc.subject.keywordPlusLINEAGE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusSIGNALS-
dc.subject.keywordPlusMOUSE-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusDIFFERENTIATION-
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