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A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2

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. Howe...

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Autores principales: Huang, Qingrui, Ji, Kai, Tian, Siyu, Wang, Fengze, Huang, Baoying, Tong, Zhou, Tan, Shuguang, Hao, Junfeng, Wang, Qihui, Tan, Wenjie, Gao, George F., Yan, Jinghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858593/
https://www.ncbi.nlm.nih.gov/pubmed/33536425
http://dx.doi.org/10.1038/s41467-021-21037-2
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author Huang, Qingrui
Ji, Kai
Tian, Siyu
Wang, Fengze
Huang, Baoying
Tong, Zhou
Tan, Shuguang
Hao, Junfeng
Wang, Qihui
Tan, Wenjie
Gao, George F.
Yan, Jinghua
author_facet Huang, Qingrui
Ji, Kai
Tian, Siyu
Wang, Fengze
Huang, Baoying
Tong, Zhou
Tan, Shuguang
Hao, Junfeng
Wang, Qihui
Tan, Wenjie
Gao, George F.
Yan, Jinghua
author_sort Huang, Qingrui
collection PubMed
description 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.
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spelling pubmed-78585932021-02-11 A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2 Huang, Qingrui Ji, Kai Tian, Siyu Wang, Fengze Huang, Baoying Tong, Zhou Tan, Shuguang Hao, Junfeng Wang, Qihui Tan, Wenjie Gao, George F. Yan, Jinghua Nat Commun Article 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. Nature Publishing Group UK 2021-02-03 /pmc/articles/PMC7858593/ /pubmed/33536425 http://dx.doi.org/10.1038/s41467-021-21037-2 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Huang, Qingrui
Ji, Kai
Tian, Siyu
Wang, Fengze
Huang, Baoying
Tong, Zhou
Tan, Shuguang
Hao, Junfeng
Wang, Qihui
Tan, Wenjie
Gao, George F.
Yan, Jinghua
A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2
title A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2
title_full A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2
title_fullStr A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2
title_full_unstemmed A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2
title_short A single-dose mRNA vaccine provides a long-term protection for hACE2 transgenic mice from SARS-CoV-2
title_sort single-dose mrna vaccine provides a long-term protection for hace2 transgenic mice from sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858593/
https://www.ncbi.nlm.nih.gov/pubmed/33536425
http://dx.doi.org/10.1038/s41467-021-21037-2
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