van der Vries Erhard, Schutten Martin, Fraaij Pieter, Boucher Charles, Osterhaus Albert
Viroscience Lab, Erasmus Medical Centre, Rotterdam, The Netherlands.
Adv Pharmacol. 2013;67:217-46. doi: 10.1016/B978-0-12-405880-4.00006-8.
Antiviral drugs for influenza therapy and prophylaxis are either of the adamantane or neuraminidase inhibitor (NAI) class. However, the NAIs are mainly prescribed nowadays, because of widespread adamantane resistance among influenza A viruses and ineffectiveness of adamantanes against influenza B. Emergence and spread of NAI resistance would further limit our therapeutic options. Taking into account the previous spread of oseltamivir-resistant viruses during the 2007/2008 season preceding the last pandemic, emergence of yet another naturally NAI-resistant influenza virus may not be an unlikely event. This previous incident also underlines the importance of resistance surveillance and asks for a better understanding of the mechanisms underlying primary resistance development. We provide an overview of the major influenza antiviral resistance mechanisms and future therapies for influenza. Here, we call for a better understanding of the effect of virus mutations upon antiviral treatment and for a tailored antiviral approach to severe influenza virus infections.
用于流感治疗和预防的抗病毒药物分为金刚烷类或神经氨酸酶抑制剂(NAI)类。然而,由于甲型流感病毒中金刚烷类耐药性广泛存在且金刚烷类对乙型流感无效,目前主要使用的是NAI类药物。NAI耐药性的出现和传播将进一步限制我们的治疗选择。考虑到在最后一次大流行之前的2007/2008季节期间曾出现过对奥司他韦耐药的病毒,另一种天然对NAI耐药的流感病毒的出现并非不可能。此前的这一事件也凸显了耐药性监测的重要性,并要求更好地理解原发性耐药产生的机制。我们概述了主要的流感抗病毒耐药机制以及流感的未来治疗方法。在此,我们呼吁更好地理解病毒突变对抗病毒治疗的影响,并针对严重流感病毒感染采取量身定制的抗病毒方法。