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特殊人群的丙型肝炎治疗。

Treatment of hepatitis C in special populations.

机构信息

Department of Gastroenterology and Hepatology, Graduate School of Medicine, Hokkaido University, North 15, West 7, Kita-ku, Sapporo, Hokkaido, 060-8638, Japan.

出版信息

J Gastroenterol. 2018 May;53(5):591-605. doi: 10.1007/s00535-017-1427-x. Epub 2018 Jan 3.

DOI:10.1007/s00535-017-1427-x
PMID:29299684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5910474/
Abstract

Hepatitis C virus (HCV) infection is one of the primary causes of liver cirrhosis and hepatocellular carcinoma. In hemodialysis patients, the rate of HCV infection is high and is moreover associated with a poor prognosis. In liver transplantation patients with HCV infection, recurrent HCV infection is universal, and re-infected HCV causes rapid progression of liver fibrosis and graft loss. Additionally, in patients with HCV and human immunodeficiency virus (HIV) co-infection, liver fibrosis progresses rapidly. Thus, there is an acute need for prompt treatment of HCV infection in these special populations (i.e., hemodialysis, liver transplantation, HIV co-infection). However, until recently, the standard anti-HCV treatment involved the use of interferon-based therapy. In these special populations, interferon-based therapies could not achieve a high rate of sustained viral response and moreover were associated with a higher rate of adverse events. With the development of novel direct-acting antivirals (DAAs), the landscape of anti-HCV therapy for special populations has changed dramatically. Indeed, in special populations treated with interferon-free DAAs, the sustained viral response rate was above 90%, with a lower incidence and severity of adverse events.

摘要

丙型肝炎病毒(HCV)感染是导致肝硬化和肝细胞癌的主要原因之一。在血液透析患者中,HCV 感染率较高,且预后较差。在 HCV 感染的肝移植患者中,HCV 复发普遍存在,再感染的 HCV 可导致肝纤维化迅速进展和移植物丢失。此外,在 HCV 和人类免疫缺陷病毒(HIV)合并感染的患者中,肝纤维化迅速进展。因此,这些特殊人群(即血液透析、肝移植、HIV 合并感染)迫切需要及时治疗 HCV 感染。然而,直到最近,标准的抗 HCV 治疗还包括使用干扰素为基础的治疗。在这些特殊人群中,基于干扰素的治疗无法实现高持续病毒应答率,且不良反应发生率更高。随着新型直接作用抗病毒药物(DAAs)的发展,特殊人群抗 HCV 治疗的格局发生了巨大变化。实际上,在接受无干扰素 DAA 治疗的特殊人群中,持续病毒应答率超过 90%,不良反应的发生率和严重程度较低。

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