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预防性丙型肝炎病毒疫苗:仍值得攀登的遥远高峰。

A prophylactic hepatitis C virus vaccine: a distant peak still worth climbing.

机构信息

Gastrointestinal Unit, Massachusetts General Hospital and Harvard Medical School, USA; Inserm Unité 1110, France; Institut de Recherche sur les Maladies Virales et Hépatiques, Université de Strasbourg, France; Institut Hospitalo-Universitaire, Pôle Hépato-digestif, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Inserm Unité 1110, France; Institut de Recherche sur les Maladies Virales et Hépatiques, Université de Strasbourg, France.

出版信息

J Hepatol. 2014 Nov;61(1 Suppl):S34-44. doi: 10.1016/j.jhep.2014.09.009. Epub 2014 Nov 3.

Abstract

Hepatitis C virus (HCV) infects an estimated more than 150 million people and is a leading cause of liver disease worldwide. The development of direct-acting antivirals (DAAs) will markedly improve the outcome of antiviral treatment with cure of the majority of treated patients. However, several hurdles remain before HCV infection can be considered a menace of the past: High treatment costs will most likely result in absent or limited access in middle and low resource countries and will lead to selective use even in wealthier countries. The limited efficacy of current HCV screening programs leads to a majority of cases being undiagnosed or diagnosed at a late stage and DAAs will not cure virus-induced end-stage liver disease such as hepatocellular carcinoma. Certain patient subgroups may not respond or not be eligible for DAA-based treatment strategies. Finally, reinfection remains possible, making control of HCV infection in people with ongoing infection risk difficult. The unmet medical needs justify continued efforts to develop an effective vaccine, protecting from chronic HCV infection as a mean to impact the epidemic on a global scale. Recent progress in the understanding of virus-host interactions provides new perspectives for vaccine development, but many critical questions remain unanswered. In this review, we focus on what is known about the immune correlates of HCV control, highlight key mechanisms of viral evasion that pose challenges for vaccine development and suggest areas of further investigation that could enable a rational approach to vaccine design. Within this context we also discuss insights from recent HCV vaccination studies and what they suggest about the best way to go forward.

摘要

丙型肝炎病毒 (HCV) 估计感染了超过 1.5 亿人,是全球范围内导致肝病的主要原因。直接作用抗病毒药物 (DAA) 的发展将显著改善抗病毒治疗的效果,使大多数接受治疗的患者得到治愈。然而,在 HCV 感染可以被认为是过去的威胁之前,仍有几个障碍需要克服:高昂的治疗费用很可能导致中低收入国家无法获得或获得有限的治疗机会,并导致即使在富裕国家也会出现选择性使用。当前 HCV 筛查计划的疗效有限,导致大多数病例未被诊断或在晚期被诊断,而 DAA 不能治愈病毒引起的终末期肝病,如肝细胞癌。某些患者亚组可能无法对 DAA 治疗策略产生反应或不符合条件。最后,再次感染仍然是可能的,这使得控制持续感染的 HCV 感染变得困难。未满足的医疗需求证明需要继续努力开发有效的疫苗,通过预防慢性 HCV 感染来影响全球范围内的 HCV 流行。最近在病毒-宿主相互作用方面的进展为疫苗开发提供了新的视角,但仍有许多关键问题尚未得到解答。在这篇综述中,我们重点关注 HCV 控制的免疫相关性方面的已知内容,强调病毒逃避的关键机制对疫苗开发构成的挑战,并提出进一步研究的领域,这些研究可能为疫苗设计提供合理的方法。在此背景下,我们还讨论了最近 HCV 疫苗接种研究的见解以及它们对前进方向的建议。

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