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首页> 外文期刊>Journal of experimental & clinical cancer research : >Analysis of intrahepatic lymphocyte subsets in a transgenic mouse model of immune-mediated hepatocarcinogenesis.
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Analysis of intrahepatic lymphocyte subsets in a transgenic mouse model of immune-mediated hepatocarcinogenesis.

机译:免疫介导的肝癌发生的转基因小鼠模型中肝内淋巴细胞亚群的分析。

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摘要

Long-term, persistent liver cell injury increases the risk for hepatocellular carcinoma (HCC) development in chronic viral hepatitis. In support of this notion, we have developed a unique animal model of chronic immune-mediated liver disease that induces hepatocellular carcinogenesis using HBV transgenic mice; however, the intrahepatic inflammatory response was not precisely evaluated. The current study demonstrated that hepatitis B surface antigen (HBsAg)-specific cytotoxic T lymphocytes (CTLs) were detected at a frequency of 0.05% of CD8+ T lymphocytes in the liver, and that monocytes/macrophages were remarkably increased as the disease developed. These results suggest that a minimal number of intrahepatic virus-specific CTLs and the recruited monocytes/macrophages may contribute to the process of chronic liver inflammation.
机译:长期持续的肝细胞损伤增加了慢性病毒性肝炎发生肝细胞癌(HCC)的风险。为了支持这一观点,我们开发了一种独特的慢性免疫介导的肝病动物模型,该模型使用HBV转基因小鼠诱导肝细胞癌变。但是,肝内炎症反应并未得到准确评估。目前的研究表明,在肝脏中以CD8 ​​+ T淋巴细胞的0.05%的频率检测到乙型肝炎表面抗原(HBsAg)特异性的细胞毒性T淋巴细胞(CTL),并且随着疾病的发展单核细胞/巨噬细胞显着增加。这些结果表明,最少数量的肝内病毒特异性CTL和募集的单核细胞/巨噬细胞可能有助于慢性肝炎的进程。

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