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丙型肝炎病毒相关性肝细胞癌:新发现与有效治疗的希望

HCV-hepatocellular carcinoma: new findings and hope for effective treatment.

作者信息

Dash Srikanta, Haque Salima, Joshi Virendra, Prabhu Ramesh, Hazari Sidhartha, Fermin Cesar, Garry Robert

机构信息

Department of Pathology and Laboratory Medicine, Tulane University Health Sciences Center, New Orleans, Louisiana 70112, USA.

出版信息

Microsc Res Tech. 2005 Nov;68(3-4):130-48. doi: 10.1002/jemt.20227.

Abstract

We present here a comprehensive review of the current literature plus our own findings about in vivo and in vitro analysis of hepatitis C virus (HCV) infection, viral pathogenesis, mechanisms of interferon action, interferon resistance, and development of new therapeutics. Chronic HCV infection is a major risk factor for the development of human hepatocellular carcinoma. Standard therapy for chronic HCV infection is the combination of interferon alpha and ribavirin. A significant number of chronic HCV patients who cannot get rid of the virus infection by interferon therapy experience long-term inflammation of the liver and scarring of liver tissue. Patients who develop cirrhosis usually have increased risk of developing liver cancer. The molecular details of why some patients do not respond to standard interferon therapy are not known. Availability of HCV cell culture model has increased our understanding on the antiviral action of interferon alpha and mechanisms of interferon resistance. Interferons alpha, beta, and gamma each inhibit replication of HCV, and the antiviral action of interferon is targeted to the highly conserved 5'UTR used by the virus to translate protein by internal ribosome entry site mechanism. Studies from different laboratories including ours suggest that HCV replication in selected clones of cells can escape interferon action. Both viral and host factors appear to be involved in the mechanisms of interferon resistance against HCV. Since interferon therapy is not effective in all chronic hepatitis C patients, alternative therapeutic strategies are needed to treat chronic hepatitis C patients not responding to interferon therapy. We also reviewed the recent development of new alternative therapeutic strategies for chronic hepatitis C, which may be available in clinical use within the next decade. There is hope that these new agents along with interferon will prevent the occurrence of hepatocellular carcinoma due to chronic persistent hepatitis C virus infection. This review is not inclusive of all important scientific publications due to space limitation.

摘要

我们在此对当前文献以及我们自己关于丙型肝炎病毒(HCV)感染的体内和体外分析、病毒发病机制、干扰素作用机制、干扰素耐药性以及新疗法开发的研究结果进行全面综述。慢性HCV感染是人类肝细胞癌发生的主要危险因素。慢性HCV感染的标准疗法是干扰素α与利巴韦林联合使用。大量无法通过干扰素疗法清除病毒感染的慢性HCV患者会经历肝脏长期炎症和肝组织瘢痕形成。发展为肝硬化的患者通常患肝癌的风险增加。一些患者对标准干扰素疗法无反应的分子细节尚不清楚。HCV细胞培养模型的可用性增进了我们对干扰素α抗病毒作用以及干扰素耐药机制的理解。干扰素α、β和γ均可抑制HCV复制,且干扰素的抗病毒作用靶向病毒通过内部核糖体进入位点机制用于翻译蛋白质的高度保守的5'UTR。包括我们实验室在内的不同实验室的研究表明,在特定细胞克隆中HCV复制可逃避干扰素作用。病毒和宿主因素似乎都参与了针对HCV的干扰素耐药机制。由于干扰素疗法并非对所有慢性丙型肝炎患者都有效,因此需要替代治疗策略来治疗对干扰素疗法无反应的慢性丙型肝炎患者。我们还综述了慢性丙型肝炎新替代治疗策略的最新进展,这些策略可能在未来十年内用于临床。有望这些新药物与干扰素一起预防因慢性持续性丙型肝炎病毒感染导致的肝细胞癌的发生。由于篇幅限制,本综述未涵盖所有重要的科学出版物。

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