Department of Drug Discovery Research, Astellas Pharma Inc, Tsukuba, Ibaraki, Japan.
Antimicrob Agents Chemother. 2012 Jul;56(7):3587-91. doi: 10.1128/AAC.00133-12. Epub 2012 Apr 23.
ASP2151 (amenamevir) is a helicase-primase inhibitor against herpes simplex virus type 1 (HSV-1), HSV-2, and varicella-zoster virus. To evaluate the anti-HSV activity of ASP2151, susceptibility testing was performed on viruses isolated from patients participating in a placebo- and valacyclovir-controlled proof-of-concept phase II study for recurrent genital herpes. A total of 156 HSV strains were isolated prior to the dosing of patients, and no preexisting variants with less susceptibility to ASP2151 or acyclovir (ACV) were detected. ASP2151 inhibited HSV-1 and HSV-2 replication with mean 50% effective concentrations (EC(50)s) of 0.043 and 0.069 μM, whereas ACV exhibited mean EC(50)s of 2.1 and 3.2 μM, respectively. Notably, the susceptibilities of HSV isolates to ASP2151 and ACV were not altered after dosing with the antiviral agents. Taken together, these results demonstrate that ASP2151 inhibits the replication of HSV clinical isolates more potently than ACV, and HSV resistant to this novel helicase-primase inhibitor as well as ACV may not easily emerge in short-term treatment for recurrent genital herpes patients.
ASP2151(amenamevir)是一种针对单纯疱疹病毒 1 型(HSV-1)、HSV-2 和水痘带状疱疹病毒的螺旋酶-引物酶抑制剂。为评估 ASP2151 的抗 HSV 活性,对参与安慰剂和伐昔洛韦对照的复发性生殖器疱疹概念验证 II 期研究的患者中分离的病毒进行了敏感性测试。在给患者用药之前,共分离出 156 株 HSV 株,未检测到对 ASP2151 或阿昔洛韦(ACV)敏感性降低的预先存在的变异体。ASP2151 抑制 HSV-1 和 HSV-2 复制的平均 50%有效浓度(EC50)分别为 0.043 和 0.069 μM,而 ACV 的平均 EC50 分别为 2.1 和 3.2 μM。值得注意的是,在给予抗病毒药物后,HSV 分离株对 ASP2151 和 ACV 的敏感性并未改变。综上所述,这些结果表明,ASP2151 抑制 HSV 临床分离株的复制比 ACV 更有效,并且对这种新型螺旋酶-引物酶抑制剂以及 ACV 耐药的 HSV 可能不易在复发性生殖器疱疹患者的短期治疗中出现。