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将老药重新用作冠状病毒的抗病毒药物。

Repurposing old drugs as antiviral agents for coronaviruses.

机构信息

Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Miaoli, Taiwan.

Animal Technology Laboratories, Agricultural Technology Research Institute, Hsinchu, Taiwan.

出版信息

Biomed J. 2020 Aug;43(4):368-374. doi: 10.1016/j.bj.2020.05.003. Epub 2020 May 23.

Abstract

BACKGROUND

New therapeutic options to address the ongoing coronavirus disease 2019 (COVID-19) pandemic are urgently needed. One possible strategy is the repurposing of existing drugs approved for other indications as antiviral agents for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Due to the commercial unavailability of SARS-CoV-2 drugs for treating COVID-19, we screened approximately 250 existing drugs or pharmacologically active compounds for their inhibitory activities against feline infectious peritonitis coronavirus (FIPV) and human coronavirus OC43 (HCoV-OC43), a human coronavirus in the same genus (Betacoronavirus) as SARS-CoV-2.

METHODS

FIPV was proliferated in feline Fcwf-4 cells and HCoV-OC43 in human HCT-8 cells. Viral proliferation was assayed by visualization of cytopathic effects on the infected Fcwf-4 cells and immunofluorescent assay for detection of the nucleocapsid proteins of HCoV-OC43 in the HCT-8 cells. The concentrations (EC) of each drug necessary to diminish viral activity to 50% of that for the untreated controls were determined. The viabilities of Fcwf-4 and HCT-8 cells were measured by crystal violet staining and MTS/PMS assay, respectively.

RESULTS

Fifteen out of the 252 drugs or pharmacologically active compounds screened were found to be active against both FIPV and HCoV-OC43, with EC values ranging from 11 nM to 75 μM. They are all old drugs as follows, anisomycin, antimycin A, atovaquone, chloroquine, conivaptan, emetine, gemcitabine, homoharringtonine, niclosamide, nitazoxanide, oligomycin, salinomycin, tilorone, valinomycin, and vismodegib.

CONCLUSION

All of the old drugs identified as having activity against FIPV and HCoV-OC43 have seen clinical use in their respective indications and are associated with known dosing schedules and adverse effect or toxicity profiles in humans. Those, when later confirmed to have an anti-viral effect on SARS-CoV-2, should be considered for immediate uses in COVID-19 patients.

摘要

背景

急需寻找新的治疗方案来应对持续的 2019 年冠状病毒病(COVID-19)大流行。一种可能的策略是将已批准用于其他适应症的现有药物重新用于治疗严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)。由于 COVID-19 治疗用 SARS-CoV-2 药物在商业上无法获得,我们筛选了大约 250 种现有药物或具有药理活性的化合物,以评估它们对猫传染性腹膜炎冠状病毒(FIPV)和人冠状病毒 OC43(HCoV-OC43)的抑制活性。FIPV 在猫源 Fcwf-4 细胞中增殖,HCoV-OC43 在人源 HCT-8 细胞中增殖。通过观察感染的 Fcwf-4 细胞的细胞病变效应和免疫荧光法检测 HCoV-OC43 的核衣壳蛋白来检测病毒增殖。确定每种药物的浓度(EC),使其对病毒的抑制活性达到未处理对照组的 50%。通过结晶紫染色和 MTS/PMS 测定分别测定 Fcwf-4 和 HCT-8 细胞的活力。

结果

在筛选的 252 种药物或具有药理活性的化合物中,有 15 种对 FIPV 和 HCoV-OC43 均具有活性,其 EC 值范围为 11 nM 至 75 μM。它们都是老药,包括放线菌酮、抗霉素 A、阿托伐醌、氯喹、康替普韦、依米丁、吉西他滨、高三尖杉酯碱、硝氯酚、硝唑尼特、寡霉素、盐霉素、替洛隆、缬氨霉素和维莫德吉。

结论

所有被鉴定对 FIPV 和 HCoV-OC43 具有活性的老药在各自的适应症中都已被临床应用,并与人类已知的剂量方案和不良反应或毒性特征相关。如果这些药物在后来被证实对 SARS-CoV-2 具有抗病毒作用,应考虑在 COVID-19 患者中立即使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08d3/7567757/415f903d9823/gr1.jpg

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