Department of Microbiology and Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Antiviral Res. 2013 Oct;100(1):120-32. doi: 10.1016/j.antiviral.2013.07.018. Epub 2013 Aug 6.
Current options for influenza antiviral therapy are limited to the neuraminidase inhibitors, and knowledge that high levels of oseltamivir resistance have been seen among previously circulating H1N1 viruses increases the urgency to find new influenza therapeutics. To feed this pipeline, assays that are appropriate for use in high-throughput screens are being developed and are discussed in this review. Particular emphasis is placed on cell-based assays that capture both inhibitors of viral functions as well as the host functions that facilitate optimal influenza virus replication. Success in this area has been fueled by a greater understanding of the genome structure of influenza viruses and the ability to generate replication-competent recombinant viruses that carry a reporter gene, allowing for easy monitoring of viral infection in a high-throughput setting. This article forms part of a symposium in Antiviral Research on "Treatment of influenza: targeting the virus or the host."
目前用于流感抗病毒治疗的选择有限,仅限于神经氨酸酶抑制剂,而此前循环的 H1N1 病毒中已发现高水平的奥司他韦耐药性,这增加了寻找新的流感治疗方法的紧迫性。为了满足这一需求,正在开发适用于高通量筛选的检测方法,并在本综述中进行了讨论。本文特别强调了基于细胞的检测方法,这些方法既能捕捉病毒功能的抑制剂,也能捕捉促进流感病毒最佳复制的宿主功能。由于对流感病毒基因组结构有了更深入的了解,以及能够生成携带报告基因的复制型重组病毒,从而能够在高通量环境中轻松监测病毒感染,这方面的工作取得了成功。本文是《抗病毒研究》关于“流感治疗:针对病毒还是宿主”专题的一部分。