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下一代丙型肝炎病毒NS5A抑制剂比布伦特斯韦的抗病毒活性及耐药性概况

Antiviral Activity and Resistance Profile of the Next-Generation Hepatitis C Virus NS5A Inhibitor Pibrentasvir.

作者信息

Ng Teresa I, Krishnan Preethi, Pilot-Matias Tami, Kati Warren, Schnell Gretja, Beyer Jill, Reisch Thomas, Lu Liangjun, Dekhtyar Tatyana, Irvin Michelle, Tripathi Rakesh, Maring Clarence, Randolph John T, Wagner Rolf, Collins Christine

机构信息

AbbVie, Inc., North Chicago, Illinois, USA

AbbVie, Inc., North Chicago, Illinois, USA.

出版信息

Antimicrob Agents Chemother. 2017 Apr 24;61(5). doi: 10.1128/AAC.02558-16. Print 2017 May.

Abstract

Pibrentasvir (ABT-530) is a novel and pan-genotypic hepatitis C virus (HCV) NS5A inhibitor with 50% effective concentration (EC) values ranging from 1.4 to 5.0 pM against HCV replicons containing NS5A from genotypes 1 to 6. Pibrentasvir demonstrated similar activity against a panel of chimeric replicons containing HCV NS5A of genotypes 1 to 6 from clinical samples. Resistance selection studies were conducted using HCV replicon cells with NS5A from genotype 1a, 1b, 2a, 2b, 3a, 4a, 5a, or 6a at a concentration of pibrentasvir that was 10- or 100-fold over its EC for the respective replicon. With pibrentasvir at 10-fold over the respective EC, only a small number of colonies (0.00015 to 0.0065% of input cells) with resistance-associated amino acid substitutions were selected in replicons containing genotype 1a, 2a, or 3a NS5A, and no viable colonies were selected in replicons containing NS5A from other genotypes. With pibrentasvir at 100-fold over the respective EC, very few colonies (0.0002% of input cells) were selected by pibrentasvir in genotype 1a replicon cells while no colonies were selected in other replicons. Pibrentasvir is active against common resistance-conferring substitutions in HCV genotypes 1 to 6 that were identified for other NS5A inhibitors, including those at key amino acid positions 28, 30, 31, or 93. The combination of pibrentasvir with HCV inhibitors of other classes produced synergistic inhibition of HCV replication. In summary, pibrentasvir is a next-generation HCV NS5A inhibitor with potent and pan-genotypic activity, and it maintains activity against common amino acid substitutions of HCV genotypes 1 to 6 that are known to confer resistance to currently approved NS5A inhibitors.

摘要

比布列斯他韦(ABT - 530)是一种新型的泛基因型丙型肝炎病毒(HCV)NS5A抑制剂,其对含有1至6型NS5A的HCV复制子的50%有效浓度(EC)值范围为1.4至5.0 pM。比布列斯他韦对一组来自临床样本的含有1至6型HCV NS5A的嵌合复制子表现出相似的活性。使用来自1a、1b、2a、2b、3a、4a、5a或6a基因型的NS5A的HCV复制子细胞进行耐药性选择研究,比布列斯他韦的浓度为其对相应复制子的EC的10倍或100倍。当比布列斯他韦浓度为相应EC的10倍时,在含有1a、2a或3a基因型NS5A的复制子中仅选择到少量具有耐药相关氨基酸替代的菌落(占输入细胞的0.00015%至0.0065%),而在含有其他基因型NS5A的复制子中未选择到存活菌落。当比布列斯他韦浓度为相应EC的100倍时,比布列斯他韦在1a基因型复制子细胞中仅选择到极少数菌落(占输入细胞的0.0002%),而在其他复制子中未选择到菌落。比布列斯他韦对1至6型HCV中已确定的其他NS5A抑制剂常见的耐药性赋予替代具有活性,包括关键氨基酸位置28、30、31或93处的替代。比布列斯他韦与其他类别的HCV抑制剂联合使用对HCV复制产生协同抑制作用。总之,比布列斯他韦是一种具有强效和泛基因型活性的下一代HCV NS5A抑制剂,并且对已知会导致对当前批准的NS5A抑制剂耐药的1至6型HCV常见氨基酸替代保持活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e38a/5404558/1271b680d0ff/zac0051761110001.jpg

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