Alford C A
Am J Med. 1982 Jul 20;73(1A):225-8. doi: 10.1016/0002-9343(82)90096-1.
As reflected in the preclinical and early clinical data, acyclovir seems destined to have a very useful role in the treatment and/or prophylaxis of herpes virus (HSV) infections in immunosuppressed humans. If the preclinical predictions can be extrapolated to varicella-zoster (V-Z) infections, acyclovir could well also play a meaningful role in therapy of V-Z infections in the immunosuppressed host; however, this conjecture awaits proof of controlled studies in humans. Clearly the usefulness of acyclovir for treatment of V-Z infections should be compared with that of adenine arabinoside (ara-A) to put into proper perspective the relative efficacies of the two drugs for future therapeutic regimens. The need for comparative studies is most important at this early stage of antiviral drug development, to avoid ethical problems that will cloud the knowledge needed to move forward in a positive way. In any event, the development of acyclovir, with its targeted approach, represents a real fundamental advance in antiviral drug development. Together with the development and deployment of ara-A, it should provide the needed impetus for a surge in the creation of new antiviral compounds for tomorrow.
正如临床前和早期临床数据所反映的那样,阿昔洛韦似乎注定在免疫抑制人群的疱疹病毒(HSV)感染治疗和/或预防中发挥非常有用的作用。如果临床前的预测能够外推至水痘 - 带状疱疹(V - Z)感染,那么阿昔洛韦在免疫抑制宿主的V - Z感染治疗中也很可能发挥重要作用;然而,这一推测有待人体对照研究的证实。显然,应将阿昔洛韦治疗V - Z感染的有效性与阿糖腺苷(ara - A)进行比较以便正确看待这两种药物在未来治疗方案中的相对疗效。在抗病毒药物研发的这一早期阶段,进行对比研究最为重要,以避免出现伦理问题,这些问题会阻碍我们以积极的方式获取推进研究所需的知识。无论如何,阿昔洛韦以其靶向治疗方法的研发代表了抗病毒药物研发的一项真正重大进展。与阿糖腺苷的研发和应用一起,它应该为未来新抗病毒化合物的大量涌现提供所需的推动力。