Regulatory T cell identity: formation and maintenance

被引:111
作者
Li, Xudong [1 ]
Zheng, Ye [1 ]
机构
[1] Salk Inst Biol Studies, Nomis Fdn Labs Immunobiol & Microbial Pathogenesi, La Jolla, CA 92037 USA
关键词
regulatory T cell; Foxp3; TCR; DNA looping; CpG methylation; TRANSCRIPTION FACTOR FOXP3; TGF-BETA; REG-CELLS; DNA METHYLATION; GENE-EXPRESSION; RETINOIC-ACID; IN-VIVO; LETHAL AUTOIMMUNITY; ENHANCER LANDSCAPE; EPIGENETIC CHANGES;
D O I
10.1016/j.it.2015.04.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T regulatory (Treg) cells are central to the maintenance of immune homeostasis. The transcription factor forkhead box P3 (Foxp3) is essential for specifying the Treg cell lineage during development, and continued expression of Foxp3 in mature Treg cells is necessary for suppressive function. Loss of Foxp3 expression in Treg cells is associated with autoimmune pathology. Here, we review recent insights into the mechanisms that maintain Treg cell stability and function, and place these findings within the broader understanding of mechanisms that establish Treg cell identity during development. We integrate emerging principles in Treg cell lineage maintenance with the mechanisms that allow Treg cells to sense and respond to varied inflammatory environments, and outline important areas of future inquiry in this context.
引用
收藏
页码:344 / 353
页数:10
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