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Recent thymic emigrants are the preferential precursors of regulatory T cells differentiated in the periphery

dc.contributor.authorPaiva, Ricardo S.
dc.contributor.authorLino, Andreia C.
dc.contributor.authorBergman, Marie-Louise
dc.contributor.authorCaramalho, Íris
dc.contributor.authorSousa, Ana E.
dc.contributor.authorZelenay, Santiago
dc.contributor.authorDemengeot, Jocelyne
dc.date.accessioned2015-09-23T11:26:19Z
dc.date.available2015-09-23T11:26:19Z
dc.date.issued2013
dc.description© 2013 National Academy of Sciences.por
dc.description.abstractMost Forkhead box P3(+) (Foxp3(+)) CD4 regulatory T cell (Treg) precursors are newly formed thymocytes that acquire Foxp3 expression on antigen encounter in the thymus. Differentiation of Treg, however, can also occur in the periphery. What limits this second layer of self- and nonself-reactive Treg production in physiological conditions remains to be understood. In this work, we tested the hypothesis that, similarly to thymic Treg, the precursors of peripheral Treg are immature T cells. We show that CD4(+)CD8(-)Foxp3(-) thymocytes and recent thymic emigrants (RTEs), contrarily to peripheral naïve mature cells, efficiently differentiate into Treg on transfer into lymphopenic mice. By varying donor and recipient mice and conducting ex vivo assays, we document that the preferential conversion of newly formed T cells does not require intrathymic preactivation, is cell-intrinsic, and correlates with low and high sensitivity to natural inhibitors and inducers of Foxp3 expression, such as IL-6, T-cell receptor triggering, and TGF-β. Finally, ex vivo analysis of human thymocytes and peripheral blood T cells revealed that human RTE and newly developed T cells share an increased potential to acquire a FOXP3(bright)CD25(high) Treg phenotype. Our findings indicating that RTEs are the precursors of Tregs differentiated in the periphery should guide the design of Treg-based therapies.eng
dc.description.sponsorshipThis work was funded by the Portuguese Research Council (FCT)under Grant PTDC/SAU-IMU/113541/2009 (to I.C.), fellowships (to R.S.P., A.C.L., and M.-L.B.), and a contract (to I.C.) and the European Union’s 7th Framework Programme (FP7/2007-2013) under Grant 241447 [Natural Immunomodulators as Novel Immunotherapies for Type 1 Diabetes (NAIMIT); to J.D.].eng
dc.identifier.citationPNAS | April 16, 2013 | vol. 110 | no. 16 | 6494-6499por
dc.identifier.issn0027-8424
dc.identifier.urihttp://dx.doi.org/10.1073/pnas.1221955110
dc.identifier.urihttp://hdl.handle.net/10451/20123
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherNational Academy of Scienceseng
dc.relationNovel immunotherapies for type 1 diabetes.
dc.subjectToleranceeng
dc.subjectDevelopmenteng
dc.subjectLymphopoiesiseng
dc.subjectPolarizationeng
dc.titleRecent thymic emigrants are the preferential precursors of regulatory T cells differentiated in the peripheryeng
dc.typejournal article
dspace.entity.typePublication
oaire.awardNumberPTDC/SAU-IMU/113541/2009
oaire.awardNumber241447
oaire.awardTitleNovel immunotherapies for type 1 diabetes.
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FSAU-IMU%2F113541%2F2009/PT
oaire.awardURIinfo:eu-repo/grantAgreement/EC/FP7/241447/EU
oaire.citation.titleProceedings of the National Academy of Scienceseng
oaire.fundingStream3599-PPCDT
oaire.fundingStreamFP7
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100008530
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameEuropean Commission
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isProjectOfPublicationd033ecfc-52e7-41ee-87b0-40f0eedb003c
relation.isProjectOfPublication0754f661-8c8f-4ba7-8e2e-81ad34f4e9fb
relation.isProjectOfPublication.latestForDiscovery0754f661-8c8f-4ba7-8e2e-81ad34f4e9fb

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