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重新审视针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的潜在可成药靶点以及在临床前研究和临床试验中重新利用治疗方法:一项全面综述。

Revisiting potential druggable targets against SARS-CoV-2 and repurposing therapeutics under preclinical study and clinical trials: A comprehensive review.

作者信息

Sohag Abdullah Al Mamun, Hannan Md Abdul, Rahman Sadaqur, Hossain Motaher, Hasan Mahmudul, Khan Md Kawsar, Khatun Amena, Dash Raju, Uddin Md Jamal

机构信息

Department of Biochemistry and Molecular Biology, Bangladesh Agricultural University, Mymensingh, 2202, Bangladesh.

Department of Anatomy, Dongguk University College of Medicine, Gyeongju, 38066, South Korea.

出版信息

Drug Dev Res. 2020 Dec;81(8):919-941. doi: 10.1002/ddr.21709. Epub 2020 Jul 6.

DOI:10.1002/ddr.21709
PMID:32632960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7361641/
Abstract

Coronavirus disease-19 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is one of the most contagious diseases in human history that has already affected millions of lives worldwide. To date, no vaccines or effective therapeutics have been discovered yet that may successfully treat COVID-19 patients or contain the transmission of the virus. Scientific communities across the globe responded rapidly and have been working relentlessly to develop drugs and vaccines, which may require considerable time. In this uncertainty, repurposing the existing antiviral drugs could be the best strategy to speed up the discovery of effective therapeutics against SARS-CoV-2. Moreover, drug repurposing may leave some vital information on druggable targets that could be capitalized in target-based drug discovery. Information on possible drug targets and the progress on therapeutic and vaccine development also needs to be updated. In this review, we revisited the druggable targets that may hold promise in the development of the anti-SARS-CoV-2 agent. Progresses on the development of potential therapeutics and vaccines that are under the preclinical studies and clinical trials have been highlighted. We anticipate that this review will provide valuable information that would help to accelerate the development of therapeutics and vaccines against SARS-CoV-2 infection.

摘要

由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的冠状病毒病-19(COVID-19)是人类历史上传染性最强的疾病之一,已经影响了全球数百万人的生命。迄今为止,尚未发现能够成功治疗COVID-19患者或遏制病毒传播的疫苗或有效疗法。全球科学界迅速做出反应,并一直在不懈努力研发药物和疫苗,这可能需要相当长的时间。在这种不确定性下,重新利用现有的抗病毒药物可能是加速发现针对SARS-CoV-2有效疗法的最佳策略。此外,药物重新利用可能会留下一些关于可成药靶点的重要信息,这些信息可用于基于靶点的药物发现。关于可能的药物靶点以及治疗和疫苗开发进展的信息也需要更新。在这篇综述中,我们重新审视了可能在抗SARS-CoV-2药物开发中具有潜力的可成药靶点。重点介绍了处于临床前研究和临床试验阶段的潜在治疗方法和疫苗的开发进展。我们预计,这篇综述将提供有价值的信息,有助于加速针对SARS-CoV-2感染的治疗方法和疫苗的开发。

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本文引用的文献

1
Feline coronavirus drug inhibits the main protease of SARS-CoV-2 and blocks virus replication.猫冠状病毒药物可抑制新型冠状病毒的主要蛋白酶并阻断病毒复制。
Nat Commun. 2020 Aug 27;11(1):4282. doi: 10.1038/s41467-020-18096-2.
2
Outcomes of Hydroxychloroquine Usage in United States Veterans Hospitalized with COVID-19.羟氯喹在美国 COVID-19 住院患者中的使用效果。
Med. 2020 Dec 18;1(1):114-127.e3. doi: 10.1016/j.medj.2020.06.001. Epub 2020 Jun 5.
3
Remdesivir for the Treatment of Covid-19 - Preliminary Report. Reply.瑞德西韦治疗新冠病毒病-初步报告。回复。
N Engl J Med. 2020 Sep 3;383(10):994. doi: 10.1056/NEJMc2022236. Epub 2020 Jul 10.
4
RETRACTED: Hydroxychloroquine or chloroquine with or without a macrolide for treatment of COVID-19: a multinational registry analysis.撤回:羟氯喹或氯喹联合或不联合大环内酯类药物治疗新型冠状病毒肺炎:一项多国注册分析
Lancet. 2020 May 22. doi: 10.1016/S0140-6736(20)31180-6.
5
Reduction and Functional Exhaustion of T Cells in Patients With Coronavirus Disease 2019 (COVID-19).新型冠状病毒病(COVID-19)患者 T 细胞减少和功能耗竭。
Front Immunol. 2020 May 1;11:827. doi: 10.3389/fimmu.2020.00827. eCollection 2020.
6
Remdesivir in adults with severe COVID-19: a randomised, double-blind, placebo-controlled, multicentre trial.瑞德西韦治疗成人重症 COVID-19 的随机、双盲、安慰剂对照、多中心临床试验。
Lancet. 2020 May 16;395(10236):1569-1578. doi: 10.1016/S0140-6736(20)31022-9. Epub 2020 Apr 29.
7
Structural basis for the inhibition of SARS-CoV-2 main protease by antineoplastic drug carmofur.新型冠状病毒主蛋白酶抑制剂卡莫氟的结构基础
Nat Struct Mol Biol. 2020 Jun;27(6):529-532. doi: 10.1038/s41594-020-0440-6. Epub 2020 May 7.
8
Structural and Evolutionary Analysis Indicate That the SARS-CoV-2 Mpro Is a Challenging Target for Small-Molecule Inhibitor Design.结构与进化分析表明,SARS-CoV-2 Mpro 是小分子抑制剂设计极具挑战性的靶标。
Int J Mol Sci. 2020 Apr 28;21(9):3099. doi: 10.3390/ijms21093099.
9
Experimental Treatment with Favipiravir for COVID-19: An Open-Label Control Study.法匹拉韦治疗新型冠状病毒肺炎的实验性治疗:一项开放标签对照研究。
Engineering (Beijing). 2020 Oct;6(10):1192-1198. doi: 10.1016/j.eng.2020.03.007. Epub 2020 Mar 18.
10
Inhibition of SARS-CoV-2 Infections in Engineered Human Tissues Using Clinical-Grade Soluble Human ACE2.使用临床级别的可溶性人血管紧张素转化酶 2 抑制工程化人类组织中的 SARS-CoV-2 感染。
Cell. 2020 May 14;181(4):905-913.e7. doi: 10.1016/j.cell.2020.04.004. Epub 2020 Apr 24.