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pubmed-article:17620362pubmed:abstractTextTo maintain immune homeostasis, the intestinal immune system has evolved redundant regulatory strategies. In this regard, the gut is home to a large number of regulatory T (T reg) cells, including the Foxp3(+) T reg cell. Therefore, we hypothesized that the gut environment preferentially supports extrathymic T reg cell development. We show that peripheral conversion of CD4(+) T cells to T reg cells occurs primarily in gut-associated lymphoid tissue (GALT) after oral exposure to antigen and in a lymphopenic environment. Dendritic cells (DCs) purified from the lamina propria (Lp; LpDCs) of the small intestine were found to promote a high level of T reg cell conversion relative to lymphoid organ-derived DCs. This enhanced conversion by LpDCs was dependent on TGF-beta and retinoic acid (RA), which is a vitamin A metabolite highly expressed in GALT. Together, these data demonstrate that the intestinal immune system has evolved a self-contained strategy to promote T reg cell neoconversion.lld:pubmed
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pubmed-article:17620362pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:17620362pubmed:articleTitleSmall intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid.lld:pubmed
pubmed-article:17620362pubmed:affiliationMucosal Immunology Unit, Laboratory of Parasitic Diseases, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.lld:pubmed
pubmed-article:17620362pubmed:publicationTypeJournal Articlelld:pubmed
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