Translational Mini-Review Series on Th17 Cells: Development of mouse and human T helper 17 cells

被引:50
|
作者
de Jong, E. [2 ]
Suddason, T. [1 ]
Lord, G. M. [1 ,3 ]
机构
[1] Kings Coll London, Dept Nephrol & Transplantat, London SE1 9RT, England
[2] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, Meibergdreef, Az Amsterdam, Netherlands
[3] Guys & St Thomas Hosp, NIHR Comprehens Biomed Res Ctr, London SE1 9RT, England
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 2010年 / 159卷 / 02期
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
autoimmunity; cytokines; differentiation; T cells; transcription factors; GROWTH-FACTOR-BETA; ROR-GAMMA-T; ARYL-HYDROCARBON RECEPTOR; HUMAN T(H)17 CELLS; TGF-BETA; RHEUMATOID-ARTHRITIS; MULTIPLE-SCLEROSIS; DENDRITIC CELLS; HOST-DEFENSE; AUTOIMMUNE ENCEPHALOMYELITIS;
D O I
10.1111/j.1365-2249.2009.04041.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
P>There has been a considerable amount of interest in the immunological community about new phenotypic subsets of CD4+ T cells, particularly cells that produce the cytokine interleukin (IL)-17 [named T helper type 17 (Th17) cells]. While the initial discovery of Th17 cells and the pathways that controlled their development was in the mouse, recent attention has shifted to the existence of these cells and the relevant upstream cytokine signals in humans. While it is clear that CD4+ T cells producing IL-17 exist in vivo, their relevance to disease pathogenesis is only just being understood. In this paper, we review the data regarding the generation of human Th17 cells in vitro and the evidence that this effector population is important in human disease states.
引用
收藏
页码:148 / 158
页数:11
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