Developmental plasticity of Foxp3+ regulatory T cells

被引:70
作者
Hori, Shohei [1 ]
机构
[1] RIKEN, Res Unit Immune Homeostasis, Res Ctr Allergy & Immunol, Yokohama, Kanagawa, Japan
关键词
TRANSCRIPTION FACTOR FOXP3; RETINOIC-ACID; CUTTING EDGE; IFN-GAMMA; TOLERANCE; DIFFERENTIATION; EXPRESSION; LINEAGE; TREG; GENERATION;
D O I
10.1016/j.coi.2010.08.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Foxp3(+) regulatory T (Treg) cells constitute a distinct lineage of T lymphocytes committed to suppressive functions thereby ensuring the robustness of self-tolerance and immune homeostasis in a changing environment Recent studies have challenged this notion by suggesting that they retain developmental plasticity to convert to Foxp3(-) helper T (Th) cells in response to environmental perturbations such as inflammation and lymphopenia However this issue of Treg cell plasticity remains controversial because unequivocal evidence for lineage reprogramming is lacking Instead available evidence supports an alternative view of plasticity based on pre-existing heterogeneity of Foxp3(+) T cells Recent studies of Foxp3 gene regulation have provided a framework to dissect the molecular mechanisms underlying Treg cell lineage commitment and plasticity
引用
收藏
页码:575 / 582
页数:8
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