生物
信使核糖核酸
病毒学
2019-20冠状病毒爆发
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)
计算生物学
基因
疾病
传染病(医学专业)
遗传学
医学
爆发
病理
作者
Na-Na Zhang,Xiao-Feng Li,Yong‐Qiang Deng,Hui Zhao,Yi-Jiao Huang,Guan Yang,Weijin Huang,Peng Gao,Chao Zhou,Rong-Rong Zhang,Yan Guo,Shi-Hui Sun,Hang Fan,Shu-Long Zu,Qi Chen,Qi He,Tian-Shu Cao,Xing‐Yao Huang,Hong-Ying Qiu,Jian-Hui Nie
出处
期刊:Cell
[Cell Press]
日期:2020-07-23
卷期号:182 (5): 1271-1283.e16
被引量:616
标识
DOI:10.1016/j.cell.2020.07.024
摘要
There is an urgent need for vaccines against coronavirus disease 2019 (COVID-19) because of the ongoing SARS-CoV-2 pandemic. Among all approaches, a messenger RNA (mRNA)-based vaccine has emerged as a rapid and versatile platform to quickly respond to this challenge. Here, we developed a lipid nanoparticle-encapsulated mRNA (mRNA-LNP) encoding the receptor binding domain (RBD) of SARS-CoV-2 as a vaccine candidate (called ARCoV). Intramuscular immunization of ARCoV mRNA-LNP elicited robust neutralizing antibodies against SARS-CoV-2 as well as a Th1-biased cellular response in mice and non-human primates. Two doses of ARCoV immunization in mice conferred complete protection against the challenge of a SARS-CoV-2 mouse-adapted strain. Additionally, ARCoV is manufactured as a liquid formulation and can be stored at room temperature for at least 1 week. ARCoV is currently being evaluated in phase 1 clinical trials.
科研通智能强力驱动
Strongly Powered by AbleSci AI