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寨卡病毒:起源、病理作用及治疗策略。

Zika Virus: Origins, Pathological Action, and Treatment Strategies.

作者信息

Gorshkov Kirill, Shiryaev Sergey A, Fertel Sophie, Lin Yi-Wen, Huang Chun-Teng, Pinto Antonella, Farhy Chen, Strongin Alex Y, Zheng Wei, Terskikh Alexey V

机构信息

National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, United States.

Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, United States.

出版信息

Front Microbiol. 2019 Jan 7;9:3252. doi: 10.3389/fmicb.2018.03252. eCollection 2018.

DOI:10.3389/fmicb.2018.03252
PMID:30666246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6330993/
Abstract

The Zika virus (ZIKV) global epidemic prompted the World Health Organization to declare it a 2016 Public Health Emergency of International Concern. The overwhelming experience over the past several years teaches us that ZIKV and the associated neurological complications represent a long-term world-wide challenge to public health. Although the number of ZIKV cases in the Western Hemisphere has dropped since 2016, the need for basic research and anti-ZIKV drug development remains strong. Re-emerging viruses like ZIKV are an ever-present threat in the 21st century where fast transcontinental travel lends itself to viral epidemics. Here, we first present the origin story for ZIKV and review the rapid progress researchers have made toward understanding of the ZIKV pathology and in the design, re-purposing, and testing-particularly -drug candidates for ZIKV prophylaxis and therapy ZIKV. Quite remarkably, a short, but intensive, drug-repurposing effort has already resulted in several readily available FDA-approved drugs that are capable of effectively combating the virus in infected adult mouse models and, most importantly, in both preventing maternal-fetal transmission and severe microcephaly in newborns in pregnant mouse models.

摘要

寨卡病毒(ZIKV)的全球流行促使世界卫生组织宣布其为2016年国际关注的突发公共卫生事件。过去几年的大量经验告诉我们,寨卡病毒及其相关的神经系统并发症对全球公共卫生构成了长期挑战。尽管自2016年以来西半球的寨卡病毒病例数有所下降,但基础研究和抗寨卡病毒药物研发的需求仍然强劲。像寨卡病毒这样重新出现的病毒在21世纪始终是一种威胁,因为快速的跨大陆旅行容易引发病毒流行。在此,我们首先介绍寨卡病毒的起源故事,并回顾研究人员在理解寨卡病毒病理学以及设计、重新利用和测试(特别是针对寨卡病毒预防和治疗的候选药物)方面所取得的快速进展。非常值得注意的是,一项简短但密集的药物重新利用努力已经产生了几种现成的、经美国食品药品监督管理局批准的药物,这些药物能够在受感染的成年小鼠模型中有效对抗该病毒,而且最重要的是,在怀孕小鼠模型中既能预防母婴传播,又能预防新生儿严重小头畸形。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca26/6330993/01efa5f4eeb7/fmicb-09-03252-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca26/6330993/6951db453253/fmicb-09-03252-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca26/6330993/01efa5f4eeb7/fmicb-09-03252-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca26/6330993/6951db453253/fmicb-09-03252-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca26/6330993/01efa5f4eeb7/fmicb-09-03252-g0002.jpg

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Sexual transmission of Zika virus and other flaviviruses: A living systematic review.寨卡病毒和其他黄病毒的性传播:一项实时系统综述。
PLoS Med. 2018 Jul 24;15(7):e1002611. doi: 10.1371/journal.pmed.1002611. eCollection 2018 Jul.
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Toll-like receptor agonist R848 blocks Zika virus replication by inducing the antiviral protein viperin.Toll 样受体激动剂 R848 通过诱导抗病毒蛋白 viperin 阻断寨卡病毒复制。
The Antiviral Activity of Polyphenols.
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Antiviral siRNA delivered using attenuated, anthrax toxin protects cells from the cytopathic effects of Zika virus.使用减毒炭疽毒素递送的抗病毒小干扰RNA可保护细胞免受寨卡病毒的细胞病变效应影响。
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