New antiviral approaches for respiratory syncytial virus and other mononegaviruses: Inhibiting the RNA polymerase

被引:50
作者
Fearns, Rachel [1 ]
Deval, Jerome [2 ]
机构
[1] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
[2] Alias BioPharma Inc, San Francisco, CA 94080 USA
关键词
Respiratory syncytial virus; Non-segmented negative-strand RNA virus; RNA-dependent RNA polymerases (RdRps); Virus inhibitors; Nucleoside analog; Non-nucleoside inhibitor; VESICULAR STOMATITIS-VIRUS; SMALL HYDROPHOBIC PROTEIN; TRANSCRIPTION ELONGATION-FACTOR; MESSENGER-RNA; T-705; FAVIPIRAVIR; EBOLA-VIRUS; NONNUCLEOSIDE INHIBITORS; METHYLTRANSFERASE DOMAIN; NUCLEOTIDE-SEQUENCES; CRYSTAL-STRUCTURE;
D O I
10.1016/j.antiviral.2016.08.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Worldwide, respiratory syncytial virus (RSV) causes severe disease in infants, the elderly, and immunocompromised people. No vaccine or effective antiviral treatment is available. RSV is a member of the non-segmented, negative-strand (NNS) group of RNA viruses and relies on its RNA-dependent RNA polymerase to transcribe and replicate its genome. Because of its essential nature and unique properties, the RSV polymerase has proven to be a good target for antiviral drugs, with one compound, ALS-8176, having already achieved clinical proof-of-concept efficacy in a human challenge study. In this article, we first provide an overview of the role of the RSV polymerase in viral mRNA transcription and genome replication. We then review past and current approaches to inhibiting the RSV polymerase, including use of nucleoside analogs and non-nucleoside inhibitors. Finally, we consider polymerase inhibitors that hold promise for treating infections with other NNS.RNA viruses, including measles and Ebola. (C) 2016 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:63 / 76
页数:14
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