单克隆抗体
表位
抗体
病毒学
体外
免疫系统
2019年冠状病毒病(COVID-19)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
免疫学
效应器
医学
生物
疾病
传染病(医学专业)
内科学
生物化学
作者
Pragya D. Yadav,Sanjeev Kumar Mendiratta,Sreelekshmy Mohandas,Arun Kumar Singh,Priya Abraham,Anita Shete,Sanjay Bandyopadhyay,Sanjay Kumar,Aashini Parikh,Pankaj Kalita,Vibhuti Sharma,Hardik Pandya,Chirag G. Patel,Mihir Patel,Swagat Soni,Suresh Giri,Mukul Jain
出处
期刊:Viruses
[Multidisciplinary Digital Publishing Institute]
日期:2021-12-03
卷期号:13 (12): 2424-2424
被引量:8
摘要
We have developed a monoclonal antibody (mAb) cocktail (ZRC-3308) comprising of ZRC3308-A7 and ZRC3308-B10 in the ratio 1:1 for COVID-19 treatment. The mAbs were designed to have reduced immune effector functions and increased circulation half-life. mAbs showed good binding affinities to non-competing epitopes on RBD of SARS-CoV-2 spike protein and were found neutralizing SARS-CoV-2 variants B.1, B.1.1.7, B.1.351, B.1.617.2, and B.1.617.2 AY.1 in vitro. The mAb cocktail demonstrated effective prophylactic and therapeutic activity against SARS-CoV-2 infection in Syrian hamsters. The antibody cocktail appears to be a promising candidate for prophylactic use and for therapy in early COVID-19 cases that have not progressed to severe disease.
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