Yang Hao, Lin Xinxin, Yu Qimeng, Awadasseid Annoor, Zhang Wen
Lab of Chemical Biology and Molecular Drug Design College of Pharmaceutical Science; Institute of Drug Development &Chemical Biology.
Lab of Chemical Biology and Molecular Drug Design College of Pharmaceutical Science; Institute of Drug Development &Chemical Biology; Zhejiang University of Technology, Hangzhou; Moganshan InstituteZhejiang University of Technology, Deqing, China.
Pharmazie. 2023 Dec 4;78(11):217-224. doi: 10.1691/ph.2023.3578.
The global pandemic of COVID-19 disease is caused by the pathogenic factor called SARS-CoV-2. Meanwhile, a series of vaccines and small-molecule drugs, including the mRNA vaccines and Paxlovid, have been approved, but their efficacy is decreased significantly due to the constant emergence of mutant viral strains. The R&D of host-directed therapeutics has great potential to overcome such limitations and provide new prevention and therapy options for patients with COVID-19 or high-risk group for SARS-CoV-2 infections. Transmembrane serine protease 2 (TMPRSS2) is belonging to a protein family with highly conserved serine protease domain whose crucial role in viral entry is to activate the spike protein of viruses to induce the fusion between host cells and viruses. In this review, we sketch the critical position of TMPRSS2 in the SARS-CoV-2 viral entry and summarize the advanced research and development of TMPRSS2 inhibitors, including repurposed drugs, as a new way to fight COVID-19.
全球新冠疫情由名为严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的致病因子引起。与此同时,包括mRNA疫苗和帕罗韦德在内的一系列疫苗和小分子药物已获批准,但由于突变病毒株不断出现,它们的疗效显著降低。宿主导向疗法的研发具有巨大潜力来克服这些限制,并为新冠患者或SARS-CoV-2感染高危人群提供新的预防和治疗选择。跨膜丝氨酸蛋白酶2(TMPRSS2)属于一个具有高度保守丝氨酸蛋白酶结构域的蛋白质家族,其在病毒进入过程中的关键作用是激活病毒的刺突蛋白,以诱导宿主细胞与病毒之间的融合。在这篇综述中,我们概述了TMPRSS2在SARS-CoV-2病毒进入过程中的关键地位,并总结了TMPRSS2抑制剂(包括重新利用的药物)作为抗击新冠的新方法的前沿研发情况。