New drug-strategies to tackle viral-host interactions for the treatment of influenza virus infections

被引:32
作者
van de Wakker, Simonides I. [1 ]
Fischer, Marcel J. E. [1 ]
Oosting, Ronald S. [2 ]
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Chem Biol & Drug Discovery, Utrecht, Netherlands
[2] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Pharmacol, Utrecht, Netherlands
关键词
Influenza A virus; Host targets; H5N1; Hyper immune reaction; Drug development; IN-VITRO; COMBINATION THERAPY; FUSOGENIC ACTIVITY; FAVIPIRAVIR T-705; NUCLEAR EXPORT; INHIBITOR; NEURAMINIDASE; OSELTAMIVIR; ENTRY; REPLICATION;
D O I
10.1016/j.ejphar.2017.05.038
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The influenza virus (IV) is a highly contagious virus causing seasonal global outbreaks affecting annually up to 20% of the world's population and leading to 250,000-500,000 deaths worldwide. Current vaccines have variable effectiveness, and, in particular during a pandemic outbreak, they are probably not available in the amounts needed to protect the world population. Therefore we need effective small molecule drugs to combat an N infection and that can be produced, in case of pandemic, rapidly and in large quantities. Unfortunately, natural occurring N becomes more and more resistant to current anti-IV drugs. And thus, there is an urgent need for development of alternative agents with new mechanisms of action. This review provides an overview of the pharmacology and effectiveness of new anti -IV agents, focusing on inhibition mechanisms directed against virus-host interactions.
引用
收藏
页码:178 / 190
页数:13
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