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Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization
The COVID-19 pandemic continues to wreak havoc as worldwide SARS-CoV-2 infection, hospitalization, and death rates climb unabated. Effective vaccines remain the most promising approach to counter SARS-CoV-2. Yet, while promising results are emerging from COVID-19 vaccine trials, the need for multipl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8134492/ https://www.ncbi.nlm.nih.gov/pubmed/34011948 http://dx.doi.org/10.1038/s42003-021-02128-8 |
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author | Chiba, Shiho Frey, Steven J. Halfmann, Peter J. Kuroda, Makoto Maemura, Tadashi Yang, Jie E. Wright, Elizabeth R. Kawaoka, Yoshihiro Kane, Ravi S. |
author_facet | Chiba, Shiho Frey, Steven J. Halfmann, Peter J. Kuroda, Makoto Maemura, Tadashi Yang, Jie E. Wright, Elizabeth R. Kawaoka, Yoshihiro Kane, Ravi S. |
author_sort | Chiba, Shiho |
collection | PubMed |
description | The COVID-19 pandemic continues to wreak havoc as worldwide SARS-CoV-2 infection, hospitalization, and death rates climb unabated. Effective vaccines remain the most promising approach to counter SARS-CoV-2. Yet, while promising results are emerging from COVID-19 vaccine trials, the need for multiple doses and the challenges associated with the widespread distribution and administration of vaccines remain concerns. Here, we engineered the coat protein of the MS2 bacteriophage and generated nanoparticles displaying multiple copies of the SARS-CoV-2 spike (S) protein. The use of these nanoparticles as vaccines generated high neutralizing antibody titers and protected Syrian hamsters from a challenge with SARS-CoV-2 after a single immunization with no infectious virus detected in the lungs. This nanoparticle-based vaccine platform thus provides protection after a single immunization and may be broadly applicable for protecting against SARS-CoV-2 and future pathogens with pandemic potential. |
format | Online Article Text |
id | pubmed-8134492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81344922021-05-24 Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization Chiba, Shiho Frey, Steven J. Halfmann, Peter J. Kuroda, Makoto Maemura, Tadashi Yang, Jie E. Wright, Elizabeth R. Kawaoka, Yoshihiro Kane, Ravi S. Commun Biol Article The COVID-19 pandemic continues to wreak havoc as worldwide SARS-CoV-2 infection, hospitalization, and death rates climb unabated. Effective vaccines remain the most promising approach to counter SARS-CoV-2. Yet, while promising results are emerging from COVID-19 vaccine trials, the need for multiple doses and the challenges associated with the widespread distribution and administration of vaccines remain concerns. Here, we engineered the coat protein of the MS2 bacteriophage and generated nanoparticles displaying multiple copies of the SARS-CoV-2 spike (S) protein. The use of these nanoparticles as vaccines generated high neutralizing antibody titers and protected Syrian hamsters from a challenge with SARS-CoV-2 after a single immunization with no infectious virus detected in the lungs. This nanoparticle-based vaccine platform thus provides protection after a single immunization and may be broadly applicable for protecting against SARS-CoV-2 and future pathogens with pandemic potential. Nature Publishing Group UK 2021-05-19 /pmc/articles/PMC8134492/ /pubmed/34011948 http://dx.doi.org/10.1038/s42003-021-02128-8 Text en © The Author(s) 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 Chiba, Shiho Frey, Steven J. Halfmann, Peter J. Kuroda, Makoto Maemura, Tadashi Yang, Jie E. Wright, Elizabeth R. Kawaoka, Yoshihiro Kane, Ravi S. Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization |
title | Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization |
title_full | Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization |
title_fullStr | Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization |
title_full_unstemmed | Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization |
title_short | Multivalent nanoparticle-based vaccines protect hamsters against SARS-CoV-2 after a single immunization |
title_sort | multivalent nanoparticle-based vaccines protect hamsters against sars-cov-2 after a single immunization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8134492/ https://www.ncbi.nlm.nih.gov/pubmed/34011948 http://dx.doi.org/10.1038/s42003-021-02128-8 |
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