T Helper 17 Cells in Autoimmune Liver Diseases

被引:25
作者
Abe, Masanori [1 ]
Hiasa, Yoichi [1 ]
Onji, Andmorikazu [1 ]
机构
[1] Ehime Univ, Grad Sch Med, Dept Gastroenterol & Metabol, To On, Ehime 7910295, Japan
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2013年
关键词
PRIMARY BILIARY-CIRRHOSIS; GROWTH-FACTOR-BETA; ROR-GAMMA-T; TH17; CELLS; TGF-BETA; INTERLEUKIN-17; PRODUCTION; SCLEROSING CHOLANGITIS; REGULATORY CELLS; MEDICAL PROGRESS; T-H-17;
D O I
10.1155/2013/607073
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
Many autoimmune diseases are driven by self-reactive T helper (Th) cells. A new population of effector CD4(+) T cells characterized by the secretion of interleukin (IL)-17, referred to as Th17 cells, has been demonstrated to be phenotypically, functionally, and developmentally distinct from Th1 and Th2 cells. Because the liver is known to be an important source of transforming growth factor-beta and IL-6, which are cytokines that are crucial for Th17 differentiation, it is very likely that Th17 cells contribute to liver inflammation and autoimmunity. In contrast, another distinct subset of T cells, regulatory T cells (Treg), downregulate immune responses and play an important role in maintaining self-tolerance. In addition, there is a reciprocal relationship between Th17 cells and Tregs, in development and effector functions, and the balance between Th17 and Treg cells can affect the outcome of immune responses, particularly in autoimmune diseases. In this review, we will focus on the latest investigative findings related to Th17 cells in autoimmune liver disease.
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页数:6
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