Pritzker School for Molecular Engineering, The University of Chicago, Chicago, IL, USA.
Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, University of Louisville, Louisville, KY, USA.
Science. 2021 Aug 20;373(6557):931-936. doi: 10.1126/science.abg5827. Epub 2021 Jul 20.
There is an urgent need for antiviral agents that treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. We screened a library of 1900 clinically safe drugs against OC43, a human beta coronavirus that causes the common cold, and evaluated the top hits against SARS-CoV-2. Twenty drugs significantly inhibited replication of both viruses in cultured human cells. Eight of these drugs inhibited the activity of the SARS-CoV-2 main protease, 3CLpro, with the most potent being masitinib, an orally bioavailable tyrosine kinase inhibitor. X-ray crystallography and biochemistry show that masitinib acts as a competitive inhibitor of 3CLpro. Mice infected with SARS-CoV-2 and then treated with masitinib showed >200-fold reduction in viral titers in the lungs and nose, as well as reduced lung inflammation. Masitinib was also effective in vitro against all tested variants of concern (B.1.1.7, B.1.351, and P.1).
目前迫切需要能够治疗严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 感染的抗病毒药物。我们筛选了针对 OC43 的 1900 种临床安全药物库,OC43 是一种导致普通感冒的人类β冠状病毒,并评估了针对 SARS-CoV-2 的顶级候选药物。有 20 种药物能显著抑制两种病毒在培养的人类细胞中的复制。其中 8 种药物抑制了 SARS-CoV-2 主蛋白酶(3CLpro)的活性,其中最有效的是马替尼,一种口服生物可利用的酪氨酸激酶抑制剂。X 射线晶体学和生物化学表明,马替尼是 3CLpro 的竞争性抑制剂。用 SARS-CoV-2 感染的小鼠在用马替尼治疗后,肺部和鼻腔中的病毒滴度降低了 200 多倍,肺部炎症也减轻了。马替尼在体外对所有测试的关注变体(B.1.1.7、B.1.351 和 P.1)也有效。