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新冠病毒药物研发应靶向病毒还是我们自身?——抗流感病毒疗法的经验教训

Target Virus or Target Ourselves for COVID-19 Drugs Discovery?-Lessons learned from anti-influenza virus therapies.

作者信息

Liao Jiayu, Way George, Madahar Vipul

机构信息

Department of Bioengineering, Bourns College of Engineering, University of California at Riverside, 900 University Avenue, Riverside, California 92521.

出版信息

Med Drug Discov. 2020 Mar;5:100037. doi: 10.1016/j.medidd.2020.100037. Epub 2020 Apr 13.

DOI:10.1016/j.medidd.2020.100037
PMID:32292909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7153514/
Abstract

The COVID-19 pandemic, after it was reported in December 2019, is a highly contagious and now spreading to over 190 countries, causing a severe public health burden. Currently, there is no vaccine or specific drug to treat COVID-19, which is caused by a novel coronavirus, SARS-2-CoV. For this emergency, the FDA has approved Remdesivir and Hydroxychloroquine for treatment of COVID-19 as Emergency Use Authorization. However, even after this pandemic, COVID-19 may still have a chance to come back. Therefore, we need to come out with new strategies for drug discovery for combating COVID-19 in the future.

摘要

2019年12月新冠疫情被报道后,它具有高度传染性,目前已蔓延至190多个国家,造成了严重的公共卫生负担。目前,尚无疫苗或特定药物可治疗由新型冠状病毒SARS-CoV-2引起的新冠疫情。针对这一紧急情况,美国食品药品监督管理局(FDA)已批准瑞德西韦和羟氯喹作为紧急使用授权用于治疗新冠疫情。然而,即使在这场疫情之后,新冠疫情仍有可能卷土重来。因此,我们需要想出新的药物研发策略,以便在未来抗击新冠疫情。

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本文引用的文献

1
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Eur J Pharmacol. 2017 Aug 15;809:178-190. doi: 10.1016/j.ejphar.2017.05.038. Epub 2017 May 19.
2
Antiviral therapies on the horizon for influenza.即将出现的流感抗病毒疗法。
Curr Opin Pharmacol. 2016 Oct;30:106-115. doi: 10.1016/j.coph.2016.08.003. Epub 2016 Aug 26.
3
Drug-Resistant and Genetic Evolutionary Analysis of Influenza Virus from Patients During the 2013 and 2014 Influenza Season in Beijing.2013年和2014年北京流感季期间患者流感病毒的耐药性及基因进化分析
Microb Drug Resist. 2017 Mar;23(2):253-260. doi: 10.1089/mdr.2015.0297. Epub 2016 May 20.
4
Nitazoxanide: a first-in-class broad-spectrum antiviral agent.硝唑尼特:一种一流的广谱抗病毒药物。
Antiviral Res. 2014 Oct;110:94-103. doi: 10.1016/j.antiviral.2014.07.014. Epub 2014 Aug 7.
5
Nitazoxanide, an antiviral thiazolide, depletes ATP-sensitive intracellular Ca(2+) stores.硝唑尼特,一种抗病毒噻唑酰胺,可耗尽ATP敏感性细胞内钙储备。
Virology. 2014 Aug;462-463:135-48. doi: 10.1016/j.virol.2014.05.015. Epub 2014 Jun 25.
6
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8
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9
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Virol J. 2010 Mar 5;7:53. doi: 10.1186/1743-422X-7-53.
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JAMA. 2009 Mar 11;301(10):1034-41. doi: 10.1001/jama.2009.294. Epub 2009 Mar 2.