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丙型肝炎病毒相关肝细胞癌:从慢性炎症到癌症。

HCV-related hepatocellular carcinoma: From chronic inflammation to cancer.

机构信息

Oncology Research Centre, Mercogliano, AV, Italy.

出版信息

Clin Immunol. 2010 Mar;134(3):237-50. doi: 10.1016/j.clim.2009.10.007. Epub 2009 Nov 11.

Abstract

Hepatitis C virus (HCV) infection is a worldwide health problem because of its incidence and pathogenicity. It might evolve into chronic disease, cirrhosis, and/or hepatocellular carcinoma (HCC) and the outcome is mainly determined by the host immune response. For viral clearance, combined innate and adaptive immune responses are required; resolution requires a vigorous, durable, polyclonal CD4(+) and CD8(+) T-cell response, with an increase in virus-specific CD8(+) T cells or cytotoxic T lymphocytes. Failure of efficient immune response can lead to chronic inflammation, tissue remodeling through cell growth, apoptosis and/or necrosis and induction of oxidative stress. Development of fibrosis and/or cirrhosis plus a microenvironment conducive to genomic instability mutations will promote neoplastic transformation. System governance derives from cellular (regulatory cells) and humoral (cytokines and chemokines) immune networks. Therefore, HCC pathogenesis may be a model to study the disease progression from chronic inflammation to cancer allowing design of new strategies targeting the immune response, thereby modifying disease outcome.

摘要

丙型肝炎病毒 (HCV) 感染是一个全球性的健康问题,因为它的发病率和致病性。它可能会发展成慢性疾病、肝硬化和/或肝癌 (HCC),其结果主要取决于宿主的免疫反应。对于病毒清除,需要联合先天和适应性免疫反应;清除需要一个强大的、持久的、多克隆的 CD4(+)和 CD8(+) T 细胞反应,增加病毒特异性 CD8(+) T 细胞或细胞毒性 T 淋巴细胞。有效的免疫反应失败可导致慢性炎症、通过细胞生长、凋亡和/或坏死诱导组织重塑以及氧化应激。纤维化和/或肝硬化的发展以及有利于基因组不稳定性突变的微环境将促进肿瘤转化。系统治理源于细胞(调节细胞)和体液(细胞因子和趋化因子)免疫网络。因此,肝癌的发病机制可能是一个从慢性炎症到癌症的疾病进展的模型,从而设计针对免疫反应的新策略,从而改变疾病的结果。

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