神经氨酸酶
病毒学
病毒
奥司他韦
金刚乙胺
大流行
金刚烷
抗病毒治疗
神经氨酸酶抑制剂
抗药性
医学
甲型流感病毒
生物
2019年冠状病毒病(COVID-19)
微生物学
传染病(医学专业)
疾病
化学
内科学
有机化学
慢性肝炎
作者
Erhard van der Vries,Martin Schutten,Pieter L. A. Fraaij,Charles A. Boucher,Albert D. M. E. Osterhaus
出处
期刊:Advances in pharmacology
日期:2013-01-01
卷期号:: 217-246
被引量:61
标识
DOI:10.1016/b978-0-12-405880-4.00006-8
摘要
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.
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