Diane S. Aschenbrenner is a COVID-19 outbreak investigator for the Baltimore County Department of Health, Baltimore, MD. She also coordinates Drug Watch :
Am J Nurs. 2021 Aug 1;121(8):22. doi: 10.1097/01.NAJ.0000767788.97481.65.
The Food and Drug Administration has granted emergency use authorization to sotrovimab for the treatment of mild to moderate COVID-19 in patients at increased risk for progression to severe illness.Sotrovimab is a monoclonal antibody that works directly against the spike protein of SARS-CoV-2 to block its attachment and entry into a human cell.
美国食品和药物管理局已批准 sotrovimab 用于治疗有进展为重症风险的 COVID-19 轻症和中度患者。Sotrovimab 是一种单克隆抗体,可直接针对 SARS-CoV-2 的刺突蛋白发挥作用,阻止其附着和进入人体细胞。