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索磷布韦和达卡他韦治疗2019冠状病毒病的综述

A mini-review on sofosbuvir and daclatasvir treatment in coronavirus disease 2019.

作者信息

Shabani M, Sadegh Ehdaei B, Fathi F, Dowran R

机构信息

Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Microbiology and Immunology Department, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, Iran.

出版信息

New Microbes New Infect. 2021 Jul;42:100895. doi: 10.1016/j.nmni.2021.100895. Epub 2021 May 7.

DOI:10.1016/j.nmni.2021.100895
PMID:33976895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8103737/
Abstract

Sofosbuvir and daclatasvir have been used successfully since 2013 for hepatitis C treatment. It has been shown by different studies that sofosbuvir can inhibit RNA polymerase of other positive-strand RNA viruses including Flaviviridae and Togaviridae. Homology between hepatitis C virus RNA polymerase and severe acute respiratory syndrome coronavirus 2 has also been established. The efficacy of sofosbuvir and daclatasvir as potential choices in treating patients with coronavirus disease 2019 and their recovery can be hypothesized.

摘要

自2013年以来,索磷布韦和达卡他韦已成功用于丙型肝炎治疗。不同研究表明,索磷布韦可抑制包括黄病毒科和披膜病毒科在内的其他正链RNA病毒的RNA聚合酶。丙型肝炎病毒RNA聚合酶与严重急性呼吸综合征冠状病毒2之间的同源性也已得到证实。可以推测索磷布韦和达卡他韦作为治疗2019冠状病毒病患者的潜在选择及其疗效。

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本文引用的文献

1
In vitro antiviral activity of the anti-HCV drugs daclatasvir and sofosbuvir against SARS-CoV-2, the aetiological agent of COVID-19.抗 HCV 药物达卡他韦和索非布韦对 COVID-19 病因 SARS-CoV-2 的体外抗病毒活性。
J Antimicrob Chemother. 2021 Jun 18;76(7):1874-1885. doi: 10.1093/jac/dkab072.
2
Nucleotide analogues as inhibitors of SARS-CoV Polymerase.核苷酸类似物作为 SARS-CoV 聚合酶抑制剂。
Pharmacol Res Perspect. 2020 Dec;8(6):e00674. doi: 10.1002/prp2.674.
3
Nucleotide Analogues as Inhibitors of SARS-CoV-2 Polymerase, a Key Drug Target for COVID-19.核苷酸类似物作为 SARS-CoV-2 聚合酶的抑制剂,是 COVID-19 的一个关键药物靶点。
J Proteome Res. 2020 Nov 6;19(11):4690-4697. doi: 10.1021/acs.jproteome.0c00392. Epub 2020 Aug 5.
4
Sofosbuvir as a potential option for the treatment of COVID-19.索磷布韦作为治疗新冠肺炎的一种潜在选择。
Acta Biomed. 2020 May 11;91(2):236-238. doi: 10.23750/abm.v91i2.9609.
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Sofosbuvir as Repurposed Antiviral Drug Against COVID-19: Why Were We Convinced to Evaluate the Drug in a Registered/Approved Clinical Trial?索非布韦作为抗新冠病毒再利用的抗病毒药物:为什么我们被说服在注册/批准的临床试验中评估该药物?
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6
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