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pubmed-article:21175595pubmed:abstractTextTransplantation tolerance induced by neonatal injection of semi-allogeneic spleen cells is associated with a pathological syndrome caused by T helper type 2 (Th2) differentiation of donor-specific CD4(+) T lymphocytes. We have shown previously that this Th2-biased response is inhibited by host CD8(+) T cells. Herein, we demonstrate that upon neonatal immunization with (A/J × BALB/c)F(1) spleen cells, BALB/c mice expand a population of CD8(+) T cells expressing both CD25 and forkhead box P3 (FoxP3) markers. In this setting, CD8(+) CD25(+) T cells predominantly produce interferon (IFN)-? and interleukin (IL)-10 and are efficient in controlling IL-4, IL-5 and IL-13 production by donor-specific CD4(+) T cells in vitro. CD8(+) FoxP3(-) T cells are single producers of IFN-? or IL-10, whereas CD8(+) FoxP3(+) T cells are double producers of IFN-? and IL-10. We further demonstrate that IFN-? and IL-10 are two major cytokines produced by CD8(+) T cells involved in the in vivo regulation of Th2-type pathology. In this setting, we conclude that neonatal alloimmunization induces the expansion of several regulatory CD8(+) T cells which may control Th2 activities via IFN-? and IL-10.lld:pubmed
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pubmed-article:21175595pubmed:copyrightInfo© 2010 The Authors. Clinical and Experimental Immunology © 2010 British Society for Immunology.lld:pubmed
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pubmed-article:21175595pubmed:articleTitleExpansion of regulatory CD8+ CD25+ T cells after neonatal alloimmunization.lld:pubmed
pubmed-article:21175595pubmed:affiliationInstitut d'Immunologie Médicale, Université Libre de Bruxelles, Gosselies, Belgium.lld:pubmed
pubmed-article:21175595pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21175595pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed