Department of Virology, University of Toyama, Toyama, Japan.
Adv Exp Med Biol. 2018;1045:103-122. doi: 10.1007/978-981-10-7230-7_6.
The discovery of acyclovir and penciclovir has led to the development of a successful systemic therapy for treating herpes simplex virus infection and varicella-zoster virus infection, and the orally available prodrugs, valacyclovir and famciclovir, have improved antiviral treatment compliance. Acyclovir and penciclovir are phosphorylated by viral thymidine kinase and are incorporated into the DNA chain by viral DNA polymerase, resulting in chain termination. Helicase-primase plays an initial step in DNA synthesis to separate the double strand into two single strands (replication fork) and is a new target of antiviral therapy. The helicase-primase inhibitors (HPIs) pritelivir and amenamevir have novel mechanisms of action, drug resistance properties, pharmacokinetic characteristics, and clinical efficacy for treating genital herpes. The clinical study of amenamevir in herpes zoster has been completed, and amenamevir has been submitted for approval for treating herpes zoster in Japan. The clinical use of HPIs will be the beginning of a new era of anti-herpes therapy.
阿昔洛韦和喷昔洛韦的发现促使人们开发出一种成功的全身治疗方法,用于治疗单纯疱疹病毒感染和水痘带状疱疹病毒感染,口服前药伐昔洛韦和泛昔洛韦提高了抗病毒治疗的依从性。阿昔洛韦和喷昔洛韦被病毒胸苷激酶磷酸化,并被病毒 DNA 聚合酶掺入 DNA 链中,导致链终止。解旋酶-引物酶在 DNA 合成中发挥初始步骤,将双链分离成两条单链(复制叉),是抗病毒治疗的新靶点。解旋酶-引物酶抑制剂(HPIs)普瑞巴林和安乃近具有新颖的作用机制、耐药特性、药代动力学特征和治疗生殖器疱疹的临床疗效。安乃近治疗带状疱疹的临床研究已经完成,安乃近已在日本提交用于治疗带状疱疹的批准申请。HPIs 的临床应用将开启抗疱疹治疗的新时代。