Tchaikapharma High Quality Medicines Inc., Science Department, 1 G.M. Dimitrov Blvd, 1172, Sofia, Bulgaria.
Medical University, Dean of Faculty of Pharmacy, 1 Sv. Kliment Ohriski Str., 5800, Pleven, Bulgaria.
Biomed Pharmacother. 2020 Nov;131:110668. doi: 10.1016/j.biopha.2020.110668. Epub 2020 Aug 24.
Coronavirus disease 2019 (COVID-19) is a kind of viral pneumonia with an unusual outbreak in Wuhan, China, which is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). There is currently no licensed antiviral treatment available to prevent human CoV infection. The widespread clinical use and existing knowledge on antiviral mechanisms of remdesivir, lopinavir/ritonavir and chloroquine/hydroxychloroquine in the treatment of previous epidemic diseases, namely, severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS), may be helpful in the combat with novel SARS-CoV-2 infection. Recent clinical evidence didn't confirm the beneficial role of lopinavir/ritonavir and chloroquine/hydroxychloroquine for COVID-19 patients and their use was reassessed. We provide an overview of the current evidence into the mechanisms of action of these available drugs which are repurposed for treatment of the new virus. Available data identifies remdesivir as an adenosine analogue that can target the RNA-dependent RNA polymerase and block viral RNA synthesis. It has been a promising antiviral drug against a wide array of RNA viruses. 3CLpro is a major CoV protease that cleaves the large replicase polyproteins during viral replication and can be targeted by the protease inhibitor lopinavir/ritonavir but the clinical effects are controversial. Chloroquine/Hydroxychloroquine could impair the replication of SARSCoV-2 by multiple mechanisms and their immunomodulatory properties could ameliorate clinical manifestations that are mediated by immune reactions of the host although its beneficial effects are under question and need to be proven at the clinical level. Existing in vitro and in vivo evidence delineate the molecular mechanisms of these drugs in CoV-infected cells. Numerous studies demonstrated the ability of remdesivir to inhibit SARS-CoV-2 replication but future research would be needed to understand the exact mode of action of lopinavir/ritonavir and chloroquine/hydroxychloroquine in SARS-CoV-2 infected cells and to use this knowledge in the treatment of the current COVID-19.
新型冠状病毒病(COVID-19)是一种在中国武汉暴发的病毒性肺炎,由严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)引起。目前尚无可用的抗病毒药物来预防人类冠状病毒感染。在治疗以往传染病(如严重急性呼吸综合征(SARS)和中东呼吸综合征(MERS))方面,瑞德西韦、洛匹那韦/利托那韦和氯喹/羟氯喹的广泛临床应用和现有的抗病毒机制知识可能有助于对抗新型 SARS-CoV-2 感染。最近的临床证据并未证实洛匹那韦/利托那韦和氯喹/羟氯喹对 COVID-19 患者的有益作用,因此对其使用进行了重新评估。我们概述了这些现有药物的作用机制的现有证据,这些药物被重新用于治疗新病毒。现有数据表明,瑞德西韦是一种可以靶向 RNA 依赖性 RNA 聚合酶并阻断病毒 RNA 合成的腺嘌呤类似物。它是一种针对广泛的 RNA 病毒的有前途的抗病毒药物。3CLpro 是一种主要的 CoV 蛋白酶,可在病毒复制过程中切割大复制酶多蛋白,并可被蛋白酶抑制剂洛匹那韦/利托那韦靶向,但临床效果存在争议。氯喹/羟氯喹可通过多种机制干扰 SARS-CoV-2 的复制,其免疫调节特性可改善由宿主免疫反应介导的临床表现,尽管其有益作用存在疑问,需要在临床水平上得到证实。现有的体外和体内证据描绘了这些药物在 CoV 感染细胞中的分子机制。许多研究表明瑞德西韦能够抑制 SARS-CoV-2 的复制,但仍需要进一步的研究来了解洛匹那韦/利托那韦和氯喹/羟氯喹在 SARS-CoV-2 感染细胞中的确切作用模式,并将这一知识应用于当前 COVID-19 的治疗。