Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid

被引:1495
作者
Sun, Cheng-Ming
Hall, Jason A.
Blank, Rebecca B.
Bouladoux, Nicolas
Oukka, Mohamed
Mora, J. Rodrigo
Belkaid, Yasmine
机构
[1] NIAID, Mucosal Immunol Unit, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[2] Univ Penn, Immunol Grad Grp, Philadelphia, PA 19104 USA
[3] Harvard Univ, Sch Med, Brigham Womens Hosp, Ctr Neurol Dis, Cambridge, MA 02139 USA
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Gastrointestinal Unit, Boston, MA 02114 USA
关键词
D O I
10.1084/jem.20070602
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To 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 Ill 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.
引用
收藏
页码:1775 / 1785
页数:11
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