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在撒哈拉以南非洲发现的高度多样化的丙型肝炎病毒株对直接作用抗病毒药物的敏感性未知。

Highly Diverse Hepatitis C Strains Detected in Sub-Saharan Africa Have Unknown Susceptibility to Direct-Acting Antiviral Treatments.

机构信息

Medical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.

Department of Medicine - University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.

出版信息

Hepatology. 2019 Apr;69(4):1426-1441. doi: 10.1002/hep.30342. Epub 2019 Mar 22.

Abstract

The global plan to eradicate hepatitis C virus (HCV) led by the World Health Organization outlines the use of highly effective direct-acting antiviral drugs (DAAs) to achieve elimination by 2030. Identifying individuals with active disease and investigation of the breadth of diversity of the virus in sub-Saharan Africa (SSA) is essential as genotypes in this region (where very few clinical trials have been carried out) are distinct from those found in other parts of the world. We undertook a population-based, nested case-control study in Uganda and obtained additional samples from the Democratic Republic of Congo (DRC) to estimate the prevalence of HCV, assess strategies for disease detection using serological and molecular techniques, and characterize genetic diversity of the virus. Using next-generation and Sanger sequencing, we aimed to identify strains circulating in East and Central Africa. A total of 7,751 Ugandan patients were initially screened for HCV, and 20 PCR-positive samples were obtained for sequencing. Serological assays were found to vary significantly in specificity for HCV. HCV strains detected in Uganda included genotype (g) 4k, g4p, g4q, and g4s and a newly identified unassigned g7 HCV strain. Two additional unassigned g7 strains were identified in patients originating from DRC (one partial and one full open reading frame sequence). These g4 and g7 strains contain nonstructural (ns) protein 3 and 5A polymorphisms associated with resistance to DAAs in other genotypes. Clinical studies are therefore indicated to investigate treatment response in infected patients. Conclusion: Although HCV prevalence and genotypes have been well characterized in patients in well-resourced countries, clinical trials are urgently required in SSA, where highly diverse g4 and g7 strains circulate.

摘要

世界卫生组织主导的全球消灭丙型肝炎病毒 (HCV) 计划概述了使用高效直接作用抗病毒药物 (DAAs) 来实现到 2030 年消除 HCV 的目标。确定患有活动性疾病的个体,并调查撒哈拉以南非洲 (SSA) 病毒多样性的广度至关重要,因为该地区(几乎没有进行过临床试验)的基因型与世界其他地区的基因型不同。我们在乌干达进行了一项基于人群的巢式病例对照研究,并从刚果民主共和国 (DRC) 获得了额外的样本,以估计 HCV 的流行率,评估使用血清学和分子技术进行疾病检测的策略,并对病毒的遗传多样性进行特征描述。我们使用下一代和 Sanger 测序技术,旨在鉴定在东非和中非流行的毒株。最初对 7751 名乌干达患者进行了 HCV 筛查,获得了 20 个 PCR 阳性样本进行测序。血清学检测在 HCV 的特异性方面存在显著差异。在乌干达检测到的 HCV 株包括基因型 (g) 4k、g4p、g4q 和 g4s 以及一种新发现的未分配 g7 HCV 株。在来自 DRC 的患者中还鉴定出另外两种未分配的 g7 株(一种部分和一种全长开放阅读框序列)。这些 g4 和 g7 株含有与其他基因型的 DAA 耐药性相关的非结构 (ns) 蛋白 3 和 5A 多态性。因此,需要进行临床研究来调查感染患者的治疗反应。结论:尽管在资源丰富的国家的患者中已经很好地描述了 HCV 的流行率和基因型,但在高度多样化的 g4 和 g7 株流行的 SSA 地区,迫切需要进行临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5f2/6492010/e8a7df6af8a3/HEP-69-1426-g001.jpg

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