Helios: still behind the clouds

被引:73
作者
Thornton, Angela M. [1 ]
Shevach, Ethan M. [1 ]
机构
[1] NIAID, Lab Immune Syst Biol, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
关键词
autoimmunity; regulation; suppression; regulatory T cells; transcription factors; REGULATORY T-CELLS; IL2; GENE-EXPRESSION; TRANSCRIPTION-FACTOR; IKAROS FAMILY; SHORT ISOFORMS; EFFECTOR; FOXP3; SUBSET; GENERATION; INDUCTION;
D O I
10.1111/imm.13115
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 (Treg) cells are a subset of CD4(+) T cells that are critical for the maintenance of self-tolerance. The forkhead box transcription factor Foxp3 is a master regulator for the Treg phenotype and function and its expression is essential in Treg cells, as the loss of Foxp3 results in lethal autoimmunity. Two major subsets of Treg cells have been described in vivo; thymus-derived Treg (tTreg) cells that develop in the thymus and peripherally induced Treg (pTreg) cells that are derived from conventional CD4(+) Foxp3(-) T cells and are converted in peripheral tissues to cells that express Foxp3 and acquire suppressive ability. The transcription factor Helios, a member of the Ikaros transcription factor family, is expressed in 60-70% of Treg cells in both mouse and man, and is believed to be a marker of tTreg cells. In this review, we discuss the role and function of Helios in Treg cells, the controversy surrounding the use of Helios as a marker of tTreg cells, and how Helios controls specific aspects of the Treg cell program.
引用
收藏
页码:161 / 170
页数:10
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