Induced CD4+Foxp3+ Regulatory T Cells in Immune Tolerance

被引:447
作者
Bilate, Angelina M. [1 ]
Lafaille, Juan J. [1 ,2 ]
机构
[1] NYU, Sch Med, Skirball Inst, Mol Pathogenesis Program,Kimmel Ctr Biol & Med, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 30 | 2012年 / 30卷
关键词
induced Treg cells; Foxp3; mucosal tolerance; inflammation; INTESTINAL INTRAEPITHELIAL LYMPHOCYTES; DE-NOVO GENERATION; IN-VIVO EXPANSION; TGF-BETA; DENDRITIC CELLS; CUTTING EDGE; ORAL TOLERANCE; RETINOIC-ACID; GERM-FREE; GUT FLORA;
D O I
10.1146/annurev-immunol-020711-075043
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T lymphocytes are essential to maintain homeostasis of the immune system, limiting the magnitude of effector responses and allowing the establishment of immunological tolerance. Two main types of regulatory T cells have been identified-natural and induced (or adaptive)-and both play significant roles in tuning down effector immune responses. Adaptive CD4(+)Foxp3(+) regulatory T (iTreg) cells develop outside the thymus under a variety of conditions. These include not only antigen presentation under subimmunogenic or noninflammatory conditions, but also chronic inflammation and infections. We speculate that the different origin of iTreg cells (noninflammatory versus inflammatory) results in distinct properties, including their stability. iTreg cells are also generated during homeostasis of the gut and in cancer, although some cancers also favor expansion of natural regulatory T (nTreg) cells. Here we review how iTreg cells develop and how they participate in immunological tolerance, contrasting, when possible, iTreg cells with nTreg cells.
引用
收藏
页码:733 / 758
页数:26
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