Unité Parasitologie et Entomologie, Département Microbiologie et Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, 13005 Marseille, France.
Aix Marseille Univ, IRD, SSA, AP-HM, VITROME, 13005 Marseille, France.
Molecules. 2020 Oct 31;25(21):5064. doi: 10.3390/molecules25215064.
In December 2019, a new severe acute respiratory syndrome coronavirus (SARS-CoV-2), causing coronavirus disease 2019 (COVID-19), emerged in Wuhan, China. Despite containment measures, SARS-CoV-2 spread in Asia, Southern Europe, then in America and currently in Africa. Identifying effective antiviral drugs is urgently needed. An efficient approach to drug discovery is to evaluate whether existing approved drugs can be efficient against SARS-CoV-2. Doxycycline, which is a second-generation tetracycline with broad-spectrum antimicrobial, antimalarial and anti-inflammatory activities, showed in vitro activity on Vero E6 cells infected with a clinically isolated SARS-CoV-2 strain (IHUMI-3) with median effective concentration (EC) of 4.5 ± 2.9 µM, compatible with oral uptake and intravenous administrations. Doxycycline interacted both on SARS-CoV-2 entry and in replication after virus entry. Besides its in vitro antiviral activity against SARS-CoV-2, doxycycline has anti-inflammatory effects by decreasing the expression of various pro-inflammatory cytokines and could prevent co-infections and superinfections due to broad-spectrum antimicrobial activity. Therefore, doxycycline could be a potential partner of COVID-19 therapies. However, these results must be taken with caution regarding the potential use in SARS-CoV-2-infected patients: it is difficult to translate in vitro study results to actual clinical treatment in patients. In vivo evaluation in animal experimental models is required to confirm the antiviral effects of doxycycline on SARS-CoV-2 and more trials of high-risk patients with moderate to severe COVID-19 infections must be initiated.
2019 年 12 月,一种新型严重急性呼吸系统综合征冠状病毒(SARS-CoV-2)在中国武汉引发了 2019 年冠状病毒病(COVID-19)。尽管采取了遏制措施,SARS-CoV-2 还是在亚洲、南欧传播,然后传播到美洲,目前正在非洲传播。迫切需要确定有效的抗病毒药物。评估现有批准的药物是否对 SARS-CoV-2 有效是一种有效的药物发现方法。强力霉素是一种具有广谱抗菌、抗疟和抗炎活性的第二代四环素,在体外对感染临床分离 SARS-CoV-2 株(IHUMI-3)的 Vero E6 细胞显示出活性,其半数有效浓度(EC)为 4.5±2.9µM,可口服和静脉给药。强力霉素在病毒进入后既作用于 SARS-CoV-2 的进入,也作用于复制。除了对 SARS-CoV-2 的体外抗病毒活性外,强力霉素还通过降低各种促炎细胞因子的表达具有抗炎作用,并可通过广谱抗菌活性预防合并感染和继发感染。因此,强力霉素可能是 COVID-19 治疗的潜在伙伴。然而,鉴于在 SARS-CoV-2 感染患者中的潜在用途,必须谨慎对待这些结果:难以将体外研究结果转化为患者的实际临床治疗。需要在动物实验模型中进行体内评估,以确认强力霉素对 SARS-CoV-2 的抗病毒作用,并必须启动更多对患有中度至重度 COVID-19 感染的高危患者的试验。