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南非丙型肝炎基因型,特别是5a基因型的核心区和NS5B区域内自然发生的耐药性突变。

Naturally occurring resistance mutations within the core and NS5B regions in hepatitis C genotypes, particularly genotype 5a, in South Africa.

作者信息

Prabdial-Sing N, Blackard J T, Puren A J, Mahomed A, Abuelhassan W, Mahlangu J, Vermeulen M, Bowyer S M

机构信息

Centre for Vaccines and Immunology, National Institute for Communicable Diseases (NICD), Sandringham, Johannesburg, South Africa; Faculty of Health Sciences, School of Pathology, Division of Virology and Communicable Diseases Surveillance, University of Witwatersrand, Johannesburg, South Africa.

Department of Internal Medicine Division of Digestive Diseases, University of Cincinnati Medical Centre, Cincinnati, OH, USA.

出版信息

Antiviral Res. 2016 Mar;127:90-8. doi: 10.1016/j.antiviral.2015.11.011. Epub 2015 Dec 17.

Abstract

Approximately 1 million South Africans are infected with Hepatitis C virus (HCV). The standard of care (SOC) in South Africa is combination therapy (pegylated interferon and ribavirin). HCV genotypes and/or mutations in the core/non-structural regions have been associated with response to therapy and/or disease progression. This study examines mutations in the core (29-280 amino acids, including ∼ 90 E1 amino acids) and NS5B (241-306 amino acids) regions on pre-treatment isolates from patients attending Johannesburg hospitals or asymptomatic South African blood donors. Diversity within known CD4+ and CD8+ T-cell epitopes was also explored. Samples grouped into subtypes 1a(N = 10) 1b(N = 12), 3a(N = 5), 4a(N = 3) and 5a(N = 61). Two mutations, associated with interferon resistance-R70Q and T110N-were present in 29 genotype 5a core sequences. No resistance mutation to NS5B nucleotide inhibitors, sofosbuvir was found. Six putative CD8+ and one CD4+ T-cell epitope sequence in the core region showed binding scores of <300 IC50nM to HLA alleles frequently observed in the South African population. No known CD8+ and CD4+ T-cell epitopes were mapped in the NS5B region. The analysis begs the question whether those infected with genotype 5a will benefit better on interferon-free combination therapies. This study provides new insight into one of the lesser studied HCV genotypes and compares the diversity seen in a large pre-treatment cohort with other subtypes.

摘要

约100万南非人感染了丙型肝炎病毒(HCV)。南非的标准治疗方案(SOC)是联合治疗(聚乙二醇化干扰素和利巴韦林)。HCV基因型和/或核心/非结构区域的突变与治疗反应和/或疾病进展有关。本研究检测了约翰内斯堡医院就诊患者或无症状南非献血者治疗前分离株的核心区域(29 - 280个氨基酸,包括约90个E1氨基酸)和NS5B区域(241 - 306个氨基酸)的突变情况。同时还探索了已知CD4 +和CD8 + T细胞表位内的多样性。样本分为1a亚型(N = 10)、1b亚型(N = 12)、3a亚型(N = 5)、4a亚型(N = 3)和5a亚型(N = 61)。在29个5a基因型核心序列中存在与干扰素耐药相关的两个突变——R70Q和T110N。未发现对NS5B核苷酸抑制剂索磷布韦的耐药突变。核心区域的6个推定CD8 +和1个CD4 + T细胞表位序列与南非人群中常见的HLA等位基因的结合分数<300 IC50nM。在NS5B区域未定位到已知的CD8 +和CD4 + T细胞表位。该分析引发了一个问题,即5a基因型感染者在无干扰素联合治疗中是否会有更好的疗效。本研究为研究较少的HCV基因型之一提供了新的见解,并将一个大型治疗前队列中的多样性与其他亚型进行了比较。

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