Joaquín Cáceres C, Cardenas-Garcia Stivalis, Carnaccini Silvia, Seibert Brittany, Rajao Daniela S, Wang Jun, Perez Daniel R
bioRxiv. 2021 Jan 27:2021.01.27.428428. doi: 10.1101/2021.01.27.428428.
The COVID-19 pandemic caused by the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is the defining global health emergency of this century. GC-376 is a M inhibitor with antiviral activity against SARS-CoV-2 . Using the K18-hACE2 mouse model, the antiviral efficacy of GC-376 against SARS-CoV-2 was evaluated. GC-376 treatment was not toxic in K18-hACE2 mice and produced milder tissue lesions, reduced viral loads, fewer presence of viral antigen, and reduced inflammation in comparison to vehicle-treated controls, most notably in the brain in mice challenged with a low virus dose. Although GC-376 was not sufficient to improve neither clinical symptoms nor survival, it did show a positive effect against SARS-CoV-2 . This study supports the notion that the K18-hACE2 mouse model is suitable to study antiviral therapies against SARS-CoV-2, and GC-376 represents a promising lead candidate for further development to treat SARS-CoV-2 infection.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病大流行是本世纪全球主要的突发公共卫生事件。GC-376是一种对SARS-CoV-2具有抗病毒活性的M蛋白酶抑制剂。利用K18-hACE2小鼠模型评估了GC-376对SARS-CoV-2的抗病毒疗效。与赋形剂处理的对照组相比,GC-376治疗对K18-hACE2小鼠无毒,且产生的组织损伤较轻,病毒载量降低,病毒抗原存在较少,炎症减轻,在低病毒剂量攻击的小鼠中,在脑中最为明显。虽然GC-376不足以改善临床症状或提高生存率,但它确实对SARS-CoV-2显示出积极作用。本研究支持K18-hACE2小鼠模型适用于研究抗SARS-CoV-2抗病毒疗法的观点,并且GC-376是进一步开发治疗SARS-CoV-2感染的有前景的先导候选药物。