Immune responses in hepatitis C virus infection and mechanisms of hepatitis C virus persistence
被引:25
作者:
Hiroishi, Kazumasa
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机构:
Showa Univ, Sch Med, Dept Gastroenterol, Shinagawa Ku, Tokyo 1428666, JapanShowa Univ, Sch Med, Dept Gastroenterol, Shinagawa Ku, Tokyo 1428666, Japan
Hiroishi, Kazumasa
[1
]
Ito, Takayoshi
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机构:
Showa Univ, Sch Med, Dept Gastroenterol, Shinagawa Ku, Tokyo 1428666, JapanShowa Univ, Sch Med, Dept Gastroenterol, Shinagawa Ku, Tokyo 1428666, Japan
Ito, Takayoshi
[1
]
Imawari, Michio
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机构:
Showa Univ, Sch Med, Dept Gastroenterol, Shinagawa Ku, Tokyo 1428666, JapanShowa Univ, Sch Med, Dept Gastroenterol, Shinagawa Ku, Tokyo 1428666, Japan
Imawari, Michio
[1
]
机构:
[1] Showa Univ, Sch Med, Dept Gastroenterol, Shinagawa Ku, Tokyo 1428666, Japan
cytotoxic T lymphocyte;
dendritic cell;
helper T cell;
natural killer cell;
regulatory T cell;
D O I:
10.1111/j.1440-1746.2008.05475.x
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Immune responses against hepatitis C virus (HCV) play a crucial role in the pathogenesis of chronic hepatitis C. HCV infection often persists and leads to chronic hepatitis and eventually cirrhosis. Accumulated data suggest that HCV proteins suppress host immune responses through the suppression of functions of immune cells, such as cytotoxic T lymphocytes, natural killer cells, and dendritic cells. They also suppress the type 1 interferon signaling system. The resulting insufficient immune responses against HCV lead to the sustained infection. The appropriate control of immune responses would contribute to the eradication of HCV and the improvement of hepatitis, but there are still many issues to be clarified. This review describes the scientific evidence to support these emerging concepts, and will touch on the implications for improving antiviral therapy.