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Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants

Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is undoubtedly the most challenging pandemic in the current century and remains a global health emergency. As the number of COVID-19 cases in the world is on the rise and variants continue to e...

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Autores principales: Liu, Cong, Rcheulishvili, Nino, Shen, Zhigao, Papukashvili, Dimitri, Xie, Fengfei, Wang, Ziqian, Wang, Xingyun, He, Yunjiao, Wang, Peng George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143166/
https://www.ncbi.nlm.nih.gov/pubmed/35631687
http://dx.doi.org/10.3390/pharmaceutics14051101
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author Liu, Cong
Rcheulishvili, Nino
Shen, Zhigao
Papukashvili, Dimitri
Xie, Fengfei
Wang, Ziqian
Wang, Xingyun
He, Yunjiao
Wang, Peng George
author_facet Liu, Cong
Rcheulishvili, Nino
Shen, Zhigao
Papukashvili, Dimitri
Xie, Fengfei
Wang, Ziqian
Wang, Xingyun
He, Yunjiao
Wang, Peng George
author_sort Liu, Cong
collection PubMed
description Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is undoubtedly the most challenging pandemic in the current century and remains a global health emergency. As the number of COVID-19 cases in the world is on the rise and variants continue to emerge, there is an urgent need for vaccines. Among all immunization approaches, mRNA vaccines have demonstrated more promising results in response to this challenge. Herein, we designed an mRNA-based vaccine encoding the receptor-binding domain (RBD) of SARS-CoV-2 encapsulated in lipid nanoparticles (LNPs). Intramuscular (i.m.) administration of the mRNA-RBD vaccine elicited broad-spectrum neutralizing antibodies and cellular responses against not only the wild-type SARS-CoV-2 virus but also Delta and Omicron variants. These results indicated that two doses of mRNA-RBD immunization conferred a strong immune response in mice against the wild-type SARS-CoV-2, while the booster dose provided a sufficient immunity against SARS-CoV-2 and its variants. Taken together, the three-dose regimen strategy of the mRNA-RBD vaccine proposed in the present study appears to be a promising reference for the development of mRNA vaccines targeting SARS-CoV-2 variants.
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spelling pubmed-91431662022-05-29 Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants Liu, Cong Rcheulishvili, Nino Shen, Zhigao Papukashvili, Dimitri Xie, Fengfei Wang, Ziqian Wang, Xingyun He, Yunjiao Wang, Peng George Pharmaceutics Article Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is undoubtedly the most challenging pandemic in the current century and remains a global health emergency. As the number of COVID-19 cases in the world is on the rise and variants continue to emerge, there is an urgent need for vaccines. Among all immunization approaches, mRNA vaccines have demonstrated more promising results in response to this challenge. Herein, we designed an mRNA-based vaccine encoding the receptor-binding domain (RBD) of SARS-CoV-2 encapsulated in lipid nanoparticles (LNPs). Intramuscular (i.m.) administration of the mRNA-RBD vaccine elicited broad-spectrum neutralizing antibodies and cellular responses against not only the wild-type SARS-CoV-2 virus but also Delta and Omicron variants. These results indicated that two doses of mRNA-RBD immunization conferred a strong immune response in mice against the wild-type SARS-CoV-2, while the booster dose provided a sufficient immunity against SARS-CoV-2 and its variants. Taken together, the three-dose regimen strategy of the mRNA-RBD vaccine proposed in the present study appears to be a promising reference for the development of mRNA vaccines targeting SARS-CoV-2 variants. MDPI 2022-05-20 /pmc/articles/PMC9143166/ /pubmed/35631687 http://dx.doi.org/10.3390/pharmaceutics14051101 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Cong
Rcheulishvili, Nino
Shen, Zhigao
Papukashvili, Dimitri
Xie, Fengfei
Wang, Ziqian
Wang, Xingyun
He, Yunjiao
Wang, Peng George
Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants
title Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants
title_full Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants
title_fullStr Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants
title_full_unstemmed Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants
title_short Development of an LNP-Encapsulated mRNA-RBD Vaccine against SARS-CoV-2 and Its Variants
title_sort development of an lnp-encapsulated mrna-rbd vaccine against sars-cov-2 and its variants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143166/
https://www.ncbi.nlm.nih.gov/pubmed/35631687
http://dx.doi.org/10.3390/pharmaceutics14051101
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