The Balance of Th17 versus Treg Cells in Autoimmunity

被引:1059
作者
Lee, Gap Ryol [1 ]
机构
[1] Sogang Univ, Dept Life Sci, 35 Baekbeom Ro, Seoul 04107, South Korea
基金
新加坡国家研究基金会;
关键词
Th17; Treg; balance; autoimmunity; ROR gamma t; Foxp3; REGULATORY T-CELLS; GROWTH-FACTOR-BETA; ROR-GAMMA-T; SEGMENTED FILAMENTOUS BACTERIA; TRANSCRIPTION FACTOR FOXP3; TGF-BETA; IN-VIVO; RHEUMATOID-ARTHRITIS; IMMUNE HOMEOSTASIS; T(H)17 CELLS;
D O I
10.3390/ijms19030730
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
T helper type 17 (Th17) cells and pTreg cells, which share a common precursor cell (the naive CD4 T cell), require a common tumor growth factor (TGF)-beta signal for initial differentiation. However, terminally differentiated cells fulfill opposite functions: Th17 cells cause autoimmunity and inflammation, whereas Treg cells inhibit these phenomena and maintain immune homeostasis. Thus, unraveling the mechanisms that affect the Th17/Treg cell balance is critical if we are to better understand autoimmunity and tolerance. Recent studies have identified many factors that influence this balance; these factors range from signaling pathways triggered by T cell receptors, costimulatory receptors, and cytokines, to various metabolic pathways and the intestinal microbiota. This review article summarizes recent advances in our understanding of the Th17/Treg balance and its implications with respect to autoimmune disease.
引用
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页数:14
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