Integrative Research Institute (IRI) for Life Sciences, Humboldt University Berlin, Berlin, Germany.
Institute of Pathology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Pharmacol Res Perspect. 2021 Feb;9(1):e00698. doi: 10.1002/prp2.698.
As the death toll of Coronavirus disease 19 (COVID-19) continues to rise worldwide, it is imperative to explore novel molecular mechanisms for targeting SARS-CoV-2. Rather than looking for drugs that directly interact with key viral proteins inhibiting its replication, an alternative and possibly add-on approach is to dismantle the host cell machinery that enables the virus to infect the host cell and spread from one cell to another. Excellent examples of such machinery are host cell proteases whose role in viral pathogenesis has been demonstrated in numerous coronaviruses. In this review, we propose two therapeutic modalities to tackle SARS-CoV-2 infections; the first is to transcriptionally modulate the expression of cellular proteases and their endogenous inhibitors and the second is to directly inhibit their enzymatic activity. We present a nonexhaustive collection of clinically investigated drugs that act by one of these mechanisms and thus represent promising candidates for preclinical in vitro testing and hopefully clinical testing in COVID-19 patients.
随着新型冠状病毒病(COVID-19)的死亡人数在全球范围内持续上升,探索针对 SARS-CoV-2 的新型分子机制至关重要。与其寻找直接与关键病毒蛋白相互作用以抑制其复制的药物,不如采用一种替代的、可能的附加方法来破坏宿主细胞机制,使病毒能够感染宿主细胞并从一个细胞传播到另一个细胞。宿主细胞蛋白酶就是这种机制的极好例子,其在多种冠状病毒中的病毒发病机制中的作用已得到证实。在这篇综述中,我们提出了两种治疗 SARS-CoV-2 感染的方法;第一种是转录调节细胞蛋白酶及其内源性抑制剂的表达,第二种是直接抑制其酶活性。我们提出了一个非详尽的临床研究药物集合,这些药物通过其中一种机制起作用,因此代表了 COVID-19 患者进行临床前体外测试和临床试验的有希望的候选药物。