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Article: Regulation of antigen-expressing dendritic cells by double negative regulatory T cells

TitleRegulation of antigen-expressing dendritic cells by double negative regulatory T cells
Authors
KeywordsDCs
CTLA4
Double negative regulatory T cells
Fas-FasL pathway
Issue Date2011
Citation
European Journal of Immunology, 2011, v. 41, n. 9, p. 2699-2708 How to Cite?
AbstractTCRαβ +CD3 +CD4 -CD8 -NK1.1 - double negative (DN) Tregs comprise 1-3% of peripheral T lymphocytes in mice and humans. It has been demonstrated that DN Tregs can suppress allo-, xeno- and auto-immune responses in an Ag-specific fashion. However, the mechanisms by which DN Tregs regulate immune responses remain elusive. Whether DN Tregs can regulate DCs has not been investigated previously. In this study, we demonstrate that DN Tregs express a high level of CTLA4 and are able to down-regulate costimulatory molecules CD80 and CD86 expressed on Ag-expressing mature DCs (mDCs). DN Tregs from CTLA4 KO mice were not able to downregulate CD80 and CD86 expression, indicating that CTLA4 is critical for DN Treg-mediated downregulation of costimulatory molecule expression on Ag-expressing mature DCs. Furthermore, DN Tregs could kill both immature and mature allogeneic DCs, as well as Ag-loaded syngeneic DCs, in an Ag-specific manner in vitro and in vivo, mainly through the Fas-FasL pathway. These data demonstrate, for the first time, that DN Tregs are potent regulators of DCs and may have the potential to be developed as a novel immune suppression treatment. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Persistent Identifierhttp://hdl.handle.net/10722/292651
ISSN
2021 Impact Factor: 6.688
2020 SCImago Journal Rankings: 2.272
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorGao, Julia Fang-
dc.contributor.authorMcIntyre, Megan S.Ford-
dc.contributor.authorJuvet, Stephen C.-
dc.contributor.authorDiao, Jun-
dc.contributor.authorLi, Xujian-
dc.contributor.authorVanama, Ramesh B.-
dc.contributor.authorMak, Tak W.-
dc.contributor.authorCattral, Mark S.-
dc.contributor.authorZhang, Li-
dc.date.accessioned2020-11-17T14:56:56Z-
dc.date.available2020-11-17T14:56:56Z-
dc.date.issued2011-
dc.identifier.citationEuropean Journal of Immunology, 2011, v. 41, n. 9, p. 2699-2708-
dc.identifier.issn0014-2980-
dc.identifier.urihttp://hdl.handle.net/10722/292651-
dc.description.abstractTCRαβ +CD3 +CD4 -CD8 -NK1.1 - double negative (DN) Tregs comprise 1-3% of peripheral T lymphocytes in mice and humans. It has been demonstrated that DN Tregs can suppress allo-, xeno- and auto-immune responses in an Ag-specific fashion. However, the mechanisms by which DN Tregs regulate immune responses remain elusive. Whether DN Tregs can regulate DCs has not been investigated previously. In this study, we demonstrate that DN Tregs express a high level of CTLA4 and are able to down-regulate costimulatory molecules CD80 and CD86 expressed on Ag-expressing mature DCs (mDCs). DN Tregs from CTLA4 KO mice were not able to downregulate CD80 and CD86 expression, indicating that CTLA4 is critical for DN Treg-mediated downregulation of costimulatory molecule expression on Ag-expressing mature DCs. Furthermore, DN Tregs could kill both immature and mature allogeneic DCs, as well as Ag-loaded syngeneic DCs, in an Ag-specific manner in vitro and in vivo, mainly through the Fas-FasL pathway. These data demonstrate, for the first time, that DN Tregs are potent regulators of DCs and may have the potential to be developed as a novel immune suppression treatment. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.-
dc.languageeng-
dc.relation.ispartofEuropean Journal of Immunology-
dc.subjectDCs-
dc.subjectCTLA4-
dc.subjectDouble negative regulatory T cells-
dc.subjectFas-FasL pathway-
dc.titleRegulation of antigen-expressing dendritic cells by double negative regulatory T cells-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1002/eji.201141428-
dc.identifier.pmid21660936-
dc.identifier.scopuseid_2-s2.0-80052151755-
dc.identifier.volume41-
dc.identifier.issue9-
dc.identifier.spage2699-
dc.identifier.epage2708-
dc.identifier.eissn1521-4141-
dc.identifier.isiWOS:000295260800035-
dc.identifier.issnl0014-2980-

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