Regulatory T cells in HBV and HCV liver diseases: implication of regulatory T lymphocytes in the control of immune response

被引:40
|
作者
Miroux, Celine [1 ]
Vausselin, Thibaut [1 ]
Delhem, Nadira [1 ]
机构
[1] CNRS, Inst Biol Lille, UMR 8161, F-59021 Lille, France
关键词
HBV; HCV; hepatocellular carcinoma; regulatory T cells; transplantation; HEPATITIS-C VIRUS; ALANINE AMINOTRANSFERASE LEVELS; HEPATOCELLULAR-CARCINOMA; INFECTED PATIENTS; PERIPHERAL-BLOOD; IN-VITRO; EFFECTOR FUNCTION; DENDRITIC CELLS; TRANSGENIC MICE; LOW-DENSITY;
D O I
10.1517/14712598.2010.529125
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Importance of the field: Hepatic cirrhosis is a frequent consequence of chronic hepatitis infection (HBV and HCV) or alcohol abuse and the most common cause of hepatocellular carcinoma (HCC). Currently, liver transplantation remains the only effective therapeutic approach for cirrhosis-related HCC patients. The evolution of the pathology strongly depends on immunological mechanisms. Areas covered in this review: Despite the presence of specific T cells, viral chronic infection and continuous tumor growth suggest a failure of immune control. It appears that direct suppression of antiviral or antitumor effector cells by regulatory T cells plays a pivotal role in the impairment of immune response. Several types of regulatory T cells have been described, natural regulatory T cells (nTreg) and induced-type 1 regulatory T cells (Tr1) being the best characterized. What the reader will gain: Currently, there is no evidence for a direct implication of regulatory T cells in the evolution of hepatitis, especially concerning chronic infection, cirrhosis late stage and HCC progress. However, recent studies show that regulatory T cells are implicated in the modulation of HBV- and HCV-associated immune response, thus, promoting HCC progress. Take home message: Therefore, nTreg and Tr1 cells seem to play an important role in the control of immune response leading to chronic hepatitis infection and progression of the pathology to cirrhosis and HCC.
引用
收藏
页码:1563 / 1572
页数:10
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