The Balance of Th17 versus Treg Cells in Autoimmunity

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초록

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.

키워드

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
제목
The Balance of Th17 versus Treg Cells in Autoimmunity
저자
Lee, Gap Ryol
DOI
10.3390/ijms19030730
발행일
2018-03
유형
Review
저널명
International Journal of Molecular Sciences
권
19
호
3