Impaired function of hepatic natural killer cells from murine chronic HBsAg carriers

被引:40
作者
Chen, YY
Wei, HM
Sun, R
Tian, ZG
机构
[1] Univ Sci & Technol China, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
[2] Shandong Univ, Sch Pharm, Jinan 250002, Peoples R China
基金
中国国家自然科学基金;
关键词
natural killer cell; hepatitis B virus; polyinosinic-polycytidylic acid; TRAIL;
D O I
10.1016/j.intimp.2005.06.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
In the present study, we demonstrated hepatic NK cells in murine chronic HBsAg carriers for the first time. It was found that the number of hepatic NK cells was decreased; natural activation of hepatic NK cells was declined; and cytotoxicity of hepatic NK cells was attenuated, which might relate to the down-regulated expression of TRAIL on hepatic NK cells. Additionally, the response of hepatic NK cells to the specific stimulation of Poly (I:C) in murine chronic HBsAg carriers was changed. The increase in anti-tumor cytotoxic activity of intrahepatic activated NK cells was markedly impaired in the transgenic mice. The transgenic mice used here had high incidence of hepatocellular carcinoma, which might result from the relative weak reactivity and impaired anti-tumor activity of NK cells in the liver. Furthermore, remarkable liver injury was observed after stimulation of Poly (I:C), demonstrating the hypersensitivity to Poly (I:C) of murine chronic HBsAg carriers which might be related to the accumulated NK cells in the liver. Why the murine chronic HBsAg carriers are characterized with impaired hepatic NK cells and the implication of the impaired hepatic NK cells in pathogenesis of HBV-related diseases, such as hepatocellular carcinoma and recrudescent hepatitis, is worth of further investigating. These results of the functions of hepatic NK cells in murine chronic HBsAg carriers would contribute to interpreting the immune responses of NK cells in the liver and the immunological mechanisms of liver diseases in human chronic HBsAg carriers. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1839 / 1852
页数:14
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