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在体外用丙型肝炎病毒 NS5A 抑制剂维帕他韦对基因型 1 至 6 的耐药性谱。

In vitro resistance profile of hepatitis C virus NS5A inhibitor velpatasvir in genotypes 1 to 6.

机构信息

Gilead Sciences, Foster City, California.

出版信息

J Viral Hepat. 2019 Aug;26(8):991-1001. doi: 10.1111/jvh.13116. Epub 2019 May 16.

Abstract

Velpatasvir is a pan-genotypic hepatitis C virus (HCV) NS5A inhibitor, which is used with sofosbuvir for treatment of infection with HCV genotypes 1-6. In vitro resistance studies were performed to characterize NS5A changes that might confer reduced velpatasvir susceptibility in vivo. Resistance selection studies using HCV replicon cells for subtypes 1a, 1b, 2a, 2b, 3a, 4a, 5a and 6a identified NS5A resistance-associated substitutions (RASs) at nine positions, most often 28M/S/T, 31F/I/M/P/V and 93D/H/N/S. In subtype 1a, RASs were selected at positions 31 and/or 93, while in subtype 1b, replicons with two or more RASs at positions 31, 54 or 93 were selected. Y93H was selected in subtypes 1a, 1b, 2a, 3a and 4a. In subtype 5a or 6a, L31P or P32L/Q was selected, respectively. Velpatasvir susceptibility of 358 replicons from genotypes 1 to 6 containing one or more NS5A RASs was also evaluated. The majority (63%) of subtypes 1a and 1b single RAS-containing replicons retained susceptibility to velpatasvir (<2.5-fold change in EC ). High levels of resistance to velpatasvir were observed for six single mutants in subtype 1a, including M28G, A92K, Y93H/N/R/W and for one mutant, A92K, in subtype 1b. Most single mutants in subtypes 2a, 2b, 3a, 4a and 5a displayed low levels of reduced velpatasvir susceptibility. High-level resistance was observed for C92T and Y93H/N in subtype 2b, Y93H/S in 3a, and L31V and P32A/L/Q/R in 6a, and several double mutants in these subtypes. Overall, velpatasvir maintained activity against most common RASs that are known to confer resistance to first-generation NS5A inhibitors.

摘要

维帕他韦是一种泛基因型丙型肝炎病毒(HCV)NS5A 抑制剂,与索磷布韦联合用于治疗 HCV 基因型 1-6 感染。为了研究体内可能导致维帕他韦敏感性降低的 NS5A 变化,进行了体外耐药性研究。使用 HCV 复制子细胞对 1a、1b、2a、2b、3a、4a、5a 和 6a 亚型进行耐药选择研究,鉴定了 9 个位置的 NS5A 耐药相关取代(RAS),最常见的是 28M/S/T、31F/I/M/P/V 和 93D/H/N/S。在 1a 亚型中,选择了 31 和/或 93 位置的 RAS,而在 1b 亚型中,选择了 2 个或更多 RAS 的复制子位于 31、54 或 93 位置。在 1a、1b、2a、3a 和 4a 亚型中选择了 Y93H。在 5a 或 6a 亚型中,分别选择了 L31P 或 P32L/Q。还评估了包含一个或多个 NS5A RAS 的基因型 1 至 6 的 358 个复制子对维帕他韦的敏感性。大多数(63%)含有单 RAS 的 1a 和 1b 亚型复制子对维帕他韦仍保持敏感性(EC 变化小于 2.5 倍)。在 1a 亚型中,包括 M28G、A92K、Y93H/N/R/W 在内的 6 个单突变体以及 1b 亚型中的 A92K 对维帕他韦的耐药性水平较高。2a、2b、3a、4a 和 5a 亚型中的大多数单突变体对维帕他韦的敏感性降低程度较低。在 2b 亚型中观察到 C92T 和 Y93H/N 的高水平耐药性,在 3a 中观察到 Y93H/S,在 6a 中观察到 L31V 和 P32A/L/Q/R,以及这些亚型中的几个双突变体。总体而言,维帕他韦对大多数已知对第一代 NS5A 抑制剂产生耐药性的常见 RAS 仍具有活性。

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