CIRI, Centre International de Recherche en Infectiologie, (Team VirPath), Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007, Lyon, France.
CIRI, Centre International de Recherche en Infectiologie, (Team VirPath), Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007, Lyon, France; Signia Therapeutics SAS, Lyon, France.
Antiviral Res. 2020 Sep;181:104878. doi: 10.1016/j.antiviral.2020.104878. Epub 2020 Jul 15.
In response to the current pandemic caused by the novel SARS-CoV-2, identifying and validating effective therapeutic strategies is more than ever necessary. We evaluated the in vitro antiviral activities of a shortlist of compounds, known for their cellular broad-spectrum activities, together with drugs that are currently under evaluation in clinical trials for COVID-19 patients. We report the antiviral effect of remdesivir, lopinavir, chloroquine, umifenovir, berberine and cyclosporine A in Vero E6 cells model of SARS-CoV-2 infection, with estimated 50% inhibitory concentrations of 0.99, 5.2, 1.38, 3.5, 10.6 and 3 μM, respectively. Virus-directed plus host-directed drug combinations were also investigated. We report a strong antagonism between remdesivir and berberine, in contrast with remdesivir/diltiazem, for which we describe high levels of synergy, with mean Loewe synergy scores of 12 and peak values above 50. Combination of host-directed drugs with direct acting antivirals underscore further validation in more physiological models, yet they open up interesting avenues for the treatment of COVID-19.
针对由新型 SARS-CoV-2 引起的当前大流行,确定和验证有效的治疗策略比以往任何时候都更加重要。我们评估了一系列已知具有细胞广谱活性的化合物以及目前正在临床试验中评估用于 COVID-19 患者的药物的体外抗病毒活性。我们报告了瑞德西韦、洛匹那韦、氯喹、乌米酚、黄连素和环孢菌素 A 在 SARS-CoV-2 感染的 Vero E6 细胞模型中的抗病毒作用,估计 50%的抑制浓度分别为 0.99、5.2、1.38、3.5、10.6 和 3μM。还研究了病毒定向和宿主定向药物联合使用。我们报告了瑞德西韦和黄连素之间存在强烈的拮抗作用,而瑞德西韦/地尔硫卓则表现出高度的协同作用,平均 Loewe 协同评分达到 12,峰值超过 50。直接作用抗病毒药物与宿主定向药物的联合使用进一步强调了在更生理模型中的验证,但它们为 COVID-19 的治疗开辟了有趣的途径。