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从慢性丙型肝炎病毒(HCV)感染者体内获取的肝脏T细胞受体γδ T细胞的特征:这些T细胞在与HCV感染相关的肝脏病理中发挥作用的证据。

Characterization of liver T-cell receptor gammadelta T cells obtained from individuals chronically infected with hepatitis C virus (HCV): evidence for these T cells playing a role in the liver pathology associated with HCV infections.

作者信息

Tseng C T, Miskovsky E, Houghton M, Klimpel G R

机构信息

Department of Microbiology, University of Texas Medical Branch, Galveston, TX 77555-1070, USA.

出版信息

Hepatology. 2001 May;33(5):1312-20. doi: 10.1053/jhep.2001.24269.

Abstract

The pathogenic mechanisms involved in viral hepatitis are not completely understood. Evidence suggests that the pathology associated with hepatitis C virus (HCV) and hepatitis B virus (HBV) infections are a result of the immune response in the liver to these viruses. The livers of patients with viral hepatitis have been shown to contain elevated numbers of T cells expressing the gamma/delta form of the T-cell receptor for antigen (TCRgammadelta). In this study, we investigated whether liver biopsy specimens obtained from individuals with viral (HCV and/or HBV) or nonviral hepatitis contained TCRgammadelta(+) T cells that could be expanded in vitro by cytokines. A high percentage of liver biopsy specimens obtained from HCV- and/or HBV-infected individuals contained high numbers of TCRgammadelta(+) T cells. In contrast, T-cell lines generated from liver biopsy tissues obtained from individuals with nonviral hepatitis or from normal controls had no preferential expansion of TCRgammadelta(+) T cells. Liver TCRgammadelta(+) T-cell lines from HCV-infected individuals had high levels of non-major histocompatibility complex (MHC)-restricted cytotoxic activity against different targets including primary hepatocytes and produced interferon gamma (IFN-gamma), tumor necrosis factor alpha (TNF-alpha), and interleukin 8 (IL-8) following activation by anti-CD3. Surprisingly, none of these liver TCRgammadelta(+) T-cell lines could recognize any of the structural or nonstructural proteins of HCV and had no cytotoxic activity against cells infected with recombinant vaccinia viruses expressing different HCV proteins. However, the crosslinking of CD81, which has been shown to bind HCV particles and E2, resulted in significant levels of IFN-gamma and TNF-alpha production by liver TCRgammadelta(+) T cells. These results suggest that TCRgammadelta(+) T cells may play a role in the liver pathology of HCV infections.

摘要

目前尚未完全了解病毒性肝炎所涉及的致病机制。有证据表明,丙型肝炎病毒(HCV)和乙型肝炎病毒(HBV)感染相关的病理变化是肝脏对这些病毒免疫反应的结果。病毒性肝炎患者的肝脏中已显示出表达抗原T细胞受体γ/δ形式(TCRγδ)的T细胞数量增加。在本研究中,我们调查了从病毒性(HCV和/或HBV)或非病毒性肝炎患者获得的肝活检标本中是否含有可被细胞因子在体外扩增的TCRγδ(+) T细胞。从HCV和/或HBV感染个体获得的肝活检标本中有很大比例含有大量TCRγδ(+) T细胞。相比之下,从非病毒性肝炎患者或正常对照获得的肝活检组织产生的T细胞系中,TCRγδ(+) T细胞没有优先扩增。来自HCV感染个体的肝脏TCRγδ(+) T细胞系对包括原代肝细胞在内的不同靶标具有高水平的非主要组织相容性复合体(MHC)限制性细胞毒性活性,并在抗CD3激活后产生γ干扰素(IFN-γ)、肿瘤坏死因子α(TNF-α)和白细胞介素8(IL-8)。令人惊讶的是,这些肝脏TCRγδ(+) T细胞系均不能识别HCV的任何结构或非结构蛋白,对感染表达不同HCV蛋白的重组痘苗病毒的细胞也没有细胞毒性活性。然而,已证明可结合HCV颗粒和E2的CD81交联导致肝脏TCRγδ(+) T细胞产生显著水平的IFN-γ和TNF-α。这些结果表明,TCRγδ(+) T细胞可能在HCV感染的肝脏病理过程中起作用。

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