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A mRNA Vaccine Encoding for a RBD 60-mer Nanoparticle Elicits Neutralizing Antibodies and Protective Immunity Against the SARS-CoV-2 Delta Variant in Transgenic K18-hACE2 Mice
Two years into the COVID-19 pandemic there is still a need for vaccines to effectively control the spread of novel SARS-CoV-2 variants and associated cases of severe disease. Here we report a messenger RNA vaccine directly encoding for a nanoparticle displaying 60 receptor binding domains (RBDs) of...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299372/ https://www.ncbi.nlm.nih.gov/pubmed/35874687 http://dx.doi.org/10.3389/fimmu.2022.912898 |
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author | Brandys, Pascal Montagutelli, Xavier Merenkova, Irena Barut, Güliz T. Thiel, Volker Schork, Nicholas J. Trüeb, Bettina Conquet, Laurine Deng, Aihua Antanasijevic, Aleksandar Lee, Hyun-Ku Valière, Martine Sindhu, Anoop Singh, Gita Herold, Jens |
author_facet | Brandys, Pascal Montagutelli, Xavier Merenkova, Irena Barut, Güliz T. Thiel, Volker Schork, Nicholas J. Trüeb, Bettina Conquet, Laurine Deng, Aihua Antanasijevic, Aleksandar Lee, Hyun-Ku Valière, Martine Sindhu, Anoop Singh, Gita Herold, Jens |
author_sort | Brandys, Pascal |
collection | PubMed |
description | Two years into the COVID-19 pandemic there is still a need for vaccines to effectively control the spread of novel SARS-CoV-2 variants and associated cases of severe disease. Here we report a messenger RNA vaccine directly encoding for a nanoparticle displaying 60 receptor binding domains (RBDs) of SARS-CoV-2 that acts as a highly effective antigen. A construct encoding the RBD of the Delta variant elicits robust neutralizing antibody response, and also provides protective immunity against the Delta variant in a widely used transgenic mouse model. We ultimately find that the proposed mRNA RBD nanoparticle-based vaccine provides a flexible platform for rapid development and will likely be of great value in combatting current and future SARS-CoV-2 variants of concern. |
format | Online Article Text |
id | pubmed-9299372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92993722022-07-21 A mRNA Vaccine Encoding for a RBD 60-mer Nanoparticle Elicits Neutralizing Antibodies and Protective Immunity Against the SARS-CoV-2 Delta Variant in Transgenic K18-hACE2 Mice Brandys, Pascal Montagutelli, Xavier Merenkova, Irena Barut, Güliz T. Thiel, Volker Schork, Nicholas J. Trüeb, Bettina Conquet, Laurine Deng, Aihua Antanasijevic, Aleksandar Lee, Hyun-Ku Valière, Martine Sindhu, Anoop Singh, Gita Herold, Jens Front Immunol Immunology Two years into the COVID-19 pandemic there is still a need for vaccines to effectively control the spread of novel SARS-CoV-2 variants and associated cases of severe disease. Here we report a messenger RNA vaccine directly encoding for a nanoparticle displaying 60 receptor binding domains (RBDs) of SARS-CoV-2 that acts as a highly effective antigen. A construct encoding the RBD of the Delta variant elicits robust neutralizing antibody response, and also provides protective immunity against the Delta variant in a widely used transgenic mouse model. We ultimately find that the proposed mRNA RBD nanoparticle-based vaccine provides a flexible platform for rapid development and will likely be of great value in combatting current and future SARS-CoV-2 variants of concern. Frontiers Media S.A. 2022-07-06 /pmc/articles/PMC9299372/ /pubmed/35874687 http://dx.doi.org/10.3389/fimmu.2022.912898 Text en Copyright © 2022 Brandys, Montagutelli, Merenkova, Barut, Thiel, Schork, Trüeb, Conquet, Deng, Antanasijevic, Lee, Valière, Sindhu, Singh and Herold https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Brandys, Pascal Montagutelli, Xavier Merenkova, Irena Barut, Güliz T. Thiel, Volker Schork, Nicholas J. Trüeb, Bettina Conquet, Laurine Deng, Aihua Antanasijevic, Aleksandar Lee, Hyun-Ku Valière, Martine Sindhu, Anoop Singh, Gita Herold, Jens A mRNA Vaccine Encoding for a RBD 60-mer Nanoparticle Elicits Neutralizing Antibodies and Protective Immunity Against the SARS-CoV-2 Delta Variant in Transgenic K18-hACE2 Mice |
title | A mRNA Vaccine Encoding for a RBD 60-mer Nanoparticle Elicits Neutralizing Antibodies and Protective Immunity Against the SARS-CoV-2 Delta Variant in Transgenic K18-hACE2 Mice |
title_full | A mRNA Vaccine Encoding for a RBD 60-mer Nanoparticle Elicits Neutralizing Antibodies and Protective Immunity Against the SARS-CoV-2 Delta Variant in Transgenic K18-hACE2 Mice |
title_fullStr | A mRNA Vaccine Encoding for a RBD 60-mer Nanoparticle Elicits Neutralizing Antibodies and Protective Immunity Against the SARS-CoV-2 Delta Variant in Transgenic K18-hACE2 Mice |
title_full_unstemmed | A mRNA Vaccine Encoding for a RBD 60-mer Nanoparticle Elicits Neutralizing Antibodies and Protective Immunity Against the SARS-CoV-2 Delta Variant in Transgenic K18-hACE2 Mice |
title_short | A mRNA Vaccine Encoding for a RBD 60-mer Nanoparticle Elicits Neutralizing Antibodies and Protective Immunity Against the SARS-CoV-2 Delta Variant in Transgenic K18-hACE2 Mice |
title_sort | mrna vaccine encoding for a rbd 60-mer nanoparticle elicits neutralizing antibodies and protective immunity against the sars-cov-2 delta variant in transgenic k18-hace2 mice |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299372/ https://www.ncbi.nlm.nih.gov/pubmed/35874687 http://dx.doi.org/10.3389/fimmu.2022.912898 |
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