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慢性丙型肝炎病毒感染患者中T细胞介导的自体肝细胞毒性

T-cell--mediated autologous hepatocytotoxicity in patients with chronic hepatitis C virus infection.

作者信息

Liaw Y F, Lee C S, Tsai S L, Liaw B W, Chen T C, Sheen I S, Chu C M

机构信息

Liver Research Unit, Chang Gung Memorial Hospital, Taipei, Taiwan.

出版信息

Hepatology. 1995 Nov;22(5):1368-73.

PMID:7590649
Abstract

Virus-specific cytotoxic T lymphocytes (CTLs) have been suggested to be responsible for the liver injuries in patients with hepatitis C virus (HCV) infection. However, there has been no report of direct evidence to substantiate this hypothesis. In this study, we performed in vitro autologous hepatocytotoxicity assay in 45 patients to examine a possible role of CTLs to HCV-infected live cells. The data were correlated with histology activity index of liver biopsy specimens. Lymphocyte subsets and hepatocyte expression of human major histocompatibility complex antigens class I and class II (HLA-I and HLA-II) were also evaluated. The immunohistochemical study showed more prominent HLA-I expression than HLA-II on hepatocytes (mean score +/- SEM:2.34 +/- 0.11 vs. 0.42 +/- 0.08; P < .01). The lymphocyte subset analysis showed that CD8+ T cells were dominant in the lobular areas showing spotty necrosis, whereas CD4+ T cells were prominent in the portal and periportal areas (P < .01). Most patients had a significant T cell-mediated cytotoxicity to hepatocytes as compared with non-T cells (percentage cytotoxicity +/- SEM:46.4 +/- 2.3 vs. 13.8 +/- 2.7; P < .001). T cell-mediated hepatocytotoxicity had a linear correlation with HAI (P < .05). The T cell-mediated cytotoxicity could be blocked by anti-CD8 (43.7% vs. 18.5%, P < .05) but not by anti-CD4 or anti-HLA-II monoclonal antibodies. These findings strongly suggest that HLA-I-restricted, CD8+ T cell-mediated hepatocytotoxicity is an important pathogenetic mechanism in patients with chronic HCV infection.

摘要

病毒特异性细胞毒性T淋巴细胞(CTLs)被认为与丙型肝炎病毒(HCV)感染患者的肝损伤有关。然而,尚无直接证据报告来证实这一假说。在本研究中,我们对45例患者进行了体外自体肝细胞毒性试验,以检验CTLs对HCV感染活细胞的可能作用。数据与肝活检标本的组织学活性指数相关。还评估了淋巴细胞亚群以及人类主要组织相容性复合体抗原I类和II类(HLA-I和HLA-II)在肝细胞中的表达。免疫组织化学研究显示,肝细胞上HLA-I的表达比HLA-II更显著(平均得分±标准误:2.34±0.11对0.42±0.08;P<0.01)。淋巴细胞亚群分析显示,在出现点状坏死的小叶区域,CD8 + T细胞占主导,而在门管区和门管周围区域,CD4 + T细胞较为突出(P<0.01)。与非T细胞相比,大多数患者对肝细胞具有显著的T细胞介导的细胞毒性(细胞毒性百分比±标准误:46.4±2.3对13.8±2.7;P<0.001)。T细胞介导的肝细胞毒性与肝组织活动指数(HAI)呈线性相关(P<0.05)。T细胞介导的细胞毒性可被抗CD8抗体阻断(43.7%对18.5%,P<0.05),但不能被抗CD4或抗HLA-II单克隆抗体阻断。这些发现有力地表明,HLA-I限制的、CD8 + T细胞介导的肝细胞毒性是慢性HCV感染患者的一种重要发病机制。

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