A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2
Qingrui Huang,
Kai Ji,
Siyu Tian,
Fengze Wang,
Baoying Huang,
Zhou Tong,
Shuguang Tan,
Junfeng Hao,
Qihui Wang,
Wenjie Tan (),
George F. Gao () and
Jinghua Yan ()
Additional contact information
Qingrui Huang: Chinese Academy of Sciences
Kai Ji: Chinese Academy of Sciences
Siyu Tian: Chinese Academy of Sciences
Fengze Wang: Chinese Academy of Sciences
Baoying Huang: China CDC
Zhou Tong: Chinese Academy of Sciences
Shuguang Tan: Chinese Academy of Sciences
Junfeng Hao: Chinese Academy of Sciences
Qihui Wang: Chinese Academy of Sciences
Wenjie Tan: China CDC
George F. Gao: University of Chinese Academy of Sciences
Jinghua Yan: Chinese Academy of Sciences
Nature Communications, 2021, vol. 12, issue 1, 1-10
Abstract:
Abstract The rapid expansion of the COVID-19 pandemic has made the development of a SARS-CoV-2 vaccine a global health and economic priority. Taking advantage of versatility and rapid development, three SARS-CoV-2 mRNA vaccine candidates have entered clinical trials with a two-dose immunization regimen. However, the waning antibody response in convalescent patients after SARS-CoV-2 infection and the emergence of human re-infection have raised widespread concerns about a possible short duration of SARS-CoV-2 vaccine protection. Here, we developed a nucleoside-modified mRNA vaccine in lipid-encapsulated form that encoded the SARS-CoV-2 RBD, termed as mRNA-RBD. A single immunization of mRNA-RBD elicited both robust neutralizing antibody and cellular responses, and conferred a near-complete protection against wild SARS-CoV-2 infection in the lungs of hACE2 transgenic mice. Noticeably, the high levels of neutralizing antibodies in BALB/c mice induced by mRNA-RBD vaccination were maintained for at least 6.5 months and conferred a long-term notable protection for hACE2 transgenic mice against SARS-CoV-2 infection in a sera transfer study. These data demonstrated that a single dose of mRNA-RBD provided long-term protection against SARS-CoV-2 challenge.
Date: 2021
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DOI: 10.1038/s41467-021-21037-2
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