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A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability
mRNA vaccines were the first to be authorized for use against SARS-CoV-2 and have since demonstrated high efficacy against serious illness and death. However, limitations in these vaccines have been recognized due to their requirement for cold storage, short durability of protection, and lack of acc...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628444/ https://www.ncbi.nlm.nih.gov/pubmed/36323666 http://dx.doi.org/10.1038/s41541-022-00549-y |
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author | Voigt, Emily A. Gerhardt, Alana Hanson, Derek Jennewein, Madeleine F. Battisti, Peter Reed, Sierra Singh, Jasneet Mohamath, Raodoh Bakken, Julie Beaver, Samuel Press, Christopher Soon-Shiong, Patrick Paddon, Christopher J. Fox, Christopher B. Casper, Corey |
author_facet | Voigt, Emily A. Gerhardt, Alana Hanson, Derek Jennewein, Madeleine F. Battisti, Peter Reed, Sierra Singh, Jasneet Mohamath, Raodoh Bakken, Julie Beaver, Samuel Press, Christopher Soon-Shiong, Patrick Paddon, Christopher J. Fox, Christopher B. Casper, Corey |
author_sort | Voigt, Emily A. |
collection | PubMed |
description | mRNA vaccines were the first to be authorized for use against SARS-CoV-2 and have since demonstrated high efficacy against serious illness and death. However, limitations in these vaccines have been recognized due to their requirement for cold storage, short durability of protection, and lack of access in low-resource regions. We have developed an easily-manufactured, potent self-amplifying RNA (saRNA) vaccine against SARS-CoV-2 that is stable at room temperature. This saRNA vaccine is formulated with a nanostructured lipid carrier (NLC), providing stability, ease of manufacturing, and protection against degradation. In preclinical studies, this saRNA/NLC vaccine induced strong humoral immunity, as demonstrated by high pseudovirus neutralization titers to the Alpha, Beta, and Delta variants of concern and induction of bone marrow-resident antibody-secreting cells. Robust Th1-biased T-cell responses were also observed after prime or homologous prime-boost in mice. Notably, the saRNA/NLC platform demonstrated thermostability when stored lyophilized at room temperature for at least 6 months and at refrigerated temperatures for at least 10 months. Taken together, this saRNA delivered by NLC represents a potential improvement in RNA technology that could allow wider access to RNA vaccines for the current COVID-19 and future pandemics. |
format | Online Article Text |
id | pubmed-9628444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96284442022-11-02 A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability Voigt, Emily A. Gerhardt, Alana Hanson, Derek Jennewein, Madeleine F. Battisti, Peter Reed, Sierra Singh, Jasneet Mohamath, Raodoh Bakken, Julie Beaver, Samuel Press, Christopher Soon-Shiong, Patrick Paddon, Christopher J. Fox, Christopher B. Casper, Corey NPJ Vaccines Article mRNA vaccines were the first to be authorized for use against SARS-CoV-2 and have since demonstrated high efficacy against serious illness and death. However, limitations in these vaccines have been recognized due to their requirement for cold storage, short durability of protection, and lack of access in low-resource regions. We have developed an easily-manufactured, potent self-amplifying RNA (saRNA) vaccine against SARS-CoV-2 that is stable at room temperature. This saRNA vaccine is formulated with a nanostructured lipid carrier (NLC), providing stability, ease of manufacturing, and protection against degradation. In preclinical studies, this saRNA/NLC vaccine induced strong humoral immunity, as demonstrated by high pseudovirus neutralization titers to the Alpha, Beta, and Delta variants of concern and induction of bone marrow-resident antibody-secreting cells. Robust Th1-biased T-cell responses were also observed after prime or homologous prime-boost in mice. Notably, the saRNA/NLC platform demonstrated thermostability when stored lyophilized at room temperature for at least 6 months and at refrigerated temperatures for at least 10 months. Taken together, this saRNA delivered by NLC represents a potential improvement in RNA technology that could allow wider access to RNA vaccines for the current COVID-19 and future pandemics. Nature Publishing Group UK 2022-11-02 /pmc/articles/PMC9628444/ /pubmed/36323666 http://dx.doi.org/10.1038/s41541-022-00549-y Text en © The Author(s) 2022, corrected publication 2022 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 Voigt, Emily A. Gerhardt, Alana Hanson, Derek Jennewein, Madeleine F. Battisti, Peter Reed, Sierra Singh, Jasneet Mohamath, Raodoh Bakken, Julie Beaver, Samuel Press, Christopher Soon-Shiong, Patrick Paddon, Christopher J. Fox, Christopher B. Casper, Corey A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability |
title | A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability |
title_full | A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability |
title_fullStr | A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability |
title_full_unstemmed | A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability |
title_short | A self-amplifying RNA vaccine against COVID-19 with long-term room-temperature stability |
title_sort | self-amplifying rna vaccine against covid-19 with long-term room-temperature stability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628444/ https://www.ncbi.nlm.nih.gov/pubmed/36323666 http://dx.doi.org/10.1038/s41541-022-00549-y |
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