Key molecules in the differentiation and commitment program of T helper 17 (Th17) cells up-to-date

被引:31
作者
Hemdan, Nasr Y. A. [1 ,2 ]
Birkenmeier, Gerd [3 ]
Wichmann, Gunnar [1 ]
机构
[1] Univ Leipzig, Fac Med, Dept Otolaryngol Head & Neck Surg, ENT Res Lab, D-04103 Leipzig, Germany
[2] Univ Alexandria, Fac Sci, Dept Zool, Alexandria 21511, Egypt
[3] Univ Leipzig, Fac Med, Inst Biochem, D-04103 Leipzig, Germany
关键词
T cell differentiation; CD4(+) Th17 cytokines; Regulatory T cells; Transcription factors; ARYL-HYDROCARBON RECEPTOR; NF-KAPPA-B; ROR-GAMMA-T; GROWTH-FACTOR-BETA; FACTOR BATF CONTROLS; TGF-BETA; CANCER-CELLS; INDUCIBLE COSTIMULATOR; MAMMALIAN TARGET; IL-17; PRODUCTION;
D O I
10.1016/j.imlet.2012.09.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The mechanisms underlying autoimmunity and cancer remain elusive. However, perpendicular evidence has been evolved in the past decade that T helper (Th)17 cells and their related molecules are implicated in initiation and induction of various disease settings including both diseases. Meanwhile, extensive research on Th17 cells elucidated various molecules including cytokines and transcription factors as well as signaling pathways involved in the differentiation, maturation, survival and ultimate commitment of Th17 cells. In the current review, we revise the mechanistic underpinnings delivered by recent research on these molecules in the Th17 differentiation/commitment concert. We emphasize on those molecules proposed as targets for attaining potential therapies of various autoimmune disorders and cancer, aiming both at dampening the dark-side of Th17 repertoire and simultaneously potentiating its benefits in the roster of the antimicrobial response. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:97 / 109
页数:13
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