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,Yuhang Jiang,Hua-Yuan Yan,Qing Ye,Xia Zhong,Xia-Lin Xue,Zhen-Yu Zha,Dongsheng Zhou,Xiao Yang,You-Chun Wang,Bo Ying,Cheng‐Feng Qin
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.