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人类免疫缺陷病毒感染个体中的丙型肝炎病毒:一种具有重大影响的新兴合并症。

Hepatitis C virus in human immunodeficiency virus-infected individuals: an emerging comorbidity with significant implications.

作者信息

Gonzalez Stevan A, Talal Andrew H

机构信息

Center for the Study of Hepatitis C and Department of Medicine, Weill Medical College of Cornell University, New York, New York10021, USA.

出版信息

Semin Liver Dis. 2003 May;23(2):149-66. doi: 10.1055/s-2003-39946.

Abstract

As antiretroviral (ARV) therapy has become more effective, hepatitis C virus (HCV) infection has emerged as an important cause of morbidity and mortality in human immunodeficiency virus (HIV)-infected individuals. HIV alters HCV clinical presentation, epidemiology, virology, and pathogenesis compared with HCV monoinfected individuals. The incidence of chronic and vertical HCV infection is increased, the rate of hepatic fibrosis progression is accelerated, peripheral and intrahepatic HCV RNA levels are increased, and end-stage liver disease (ESLD) and cirrhosis develop more rapidly in coinfected individuals. Based on these observations, combined with the increased efficacy of ARV therapy, several societies have recommended the diagnosis and treatment of HCV in coinfected individuals. HCV treatment with nonspecific antivirals, pegylated interferon alpha (PEG-IFN) and ribavirin (RBV), is more complex in coinfected individuals compared with monoinfected individuals because these regimens appear to have decreased efficacy and the incidence of complications is increased. Although new HCV-specific regimens show early promise in HCV monoinfected individuals, it is likely that these agents will be used in combination with nonspecific therapies and additional studies will be required to evaluate their efficacy in coinfected individuals.

摘要

随着抗逆转录病毒(ARV)疗法变得更加有效,丙型肝炎病毒(HCV)感染已成为人类免疫缺陷病毒(HIV)感染者发病和死亡的重要原因。与单纯感染HCV的个体相比,HIV改变了HCV的临床表现、流行病学、病毒学和发病机制。慢性和垂直HCV感染的发生率增加,肝纤维化进展速度加快,外周血和肝内HCV RNA水平升高,合并感染个体中终末期肝病(ESLD)和肝硬化的发展更为迅速。基于这些观察结果,再加上ARV疗法疗效的提高,多个学会建议对合并感染个体进行HCV的诊断和治疗。与单纯感染个体相比,使用非特异性抗病毒药物聚乙二醇化干扰素α(PEG-IFN)和利巴韦林(RBV)治疗HCV在合并感染个体中更为复杂,因为这些治疗方案的疗效似乎降低,且并发症的发生率增加。尽管新的HCV特异性治疗方案在单纯感染HCV的个体中显示出早期前景,但这些药物可能会与非特异性疗法联合使用,并且需要更多研究来评估它们在合并感染个体中的疗效。

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