T cell immunopathogenesis and immunotherapeutic strategies for chronic hepatitis B virus infection

被引:40
|
作者
Shimizu, Yukihiro [1 ]
机构
[1] Takaoka City Hosp, Gastroenterol Unit, Takaoka, Toyama 9338550, Japan
关键词
T cells; Immunopathogenesis; Immunotherapy; Hepatitis B virus infection; COLONY-STIMULATING FACTOR; CHRONIC HBV INFECTION; TRANSGENIC MICE; COMBINATION THERAPY; THYMOSIN ALPHA-1; VIRAL-HEPATITIS; IMMUNE-RESPONSE; DENDRITIC CELLS; LAMIVUDINE TREATMENT; ANTIVIRAL THERAPY;
D O I
10.3748/wjg.v18.i20.2443
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatitis B is caused by the host immune response and T cells play a major role in the immunopathogenesis. More importantly, T cells not only destroy hepatocytes infected by hepatitis B virus (HBV), but also control HBV replication or eradicate HBV in a noncytolytic manner. Therefore, analysis of T cell immune response during acute and chronic HBV infection is important to develop a strategy for successful viral control, which could lead to immunotherapy for terminating persistent HBV infection. There have been many attempts at immunotherapy for chronic HBV infection, and some have shown promising results. High viral load has been shown to suppress antiviral immune responses and immunoinhibitory signals have been recently elucidated, therefore, viral suppression by nucleos(t)ide analogs, stimulation of antiviral immune response, and suppression of the immunoinhibitory signals must be combined to achieve desirable antiviral effects. (C) 2012 Baishideng. All rights reserved.
引用
收藏
页码:2443 / 2451
页数:9
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