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Development of a pentavalent broadly protective nucleoside-modified mRNA vaccine against influenza B viruses

Messenger RNA (mRNA) vaccines represent a new, effective vaccine platform with high capacity for rapid development. Generation of a universal influenza virus vaccine with the potential to elicit long-lasting, broadly cross-reactive immune responses is a necessity for reducing influenza-associated mo...

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Autores principales: Pardi, Norbert, Carreño, Juan Manuel, O’Dell, George, Tan, Jessica, Bajusz, Csaba, Muramatsu, Hiromi, Rijnink, Willemijn, Strohmeier, Shirin, Loganathan, Madhumathi, Bielak, Dominika, Sung, Molly M. H., Tam, Ying K., Krammer, Florian, McMahon, Meagan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362976/
https://www.ncbi.nlm.nih.gov/pubmed/35945226
http://dx.doi.org/10.1038/s41467-022-32149-8
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author Pardi, Norbert
Carreño, Juan Manuel
O’Dell, George
Tan, Jessica
Bajusz, Csaba
Muramatsu, Hiromi
Rijnink, Willemijn
Strohmeier, Shirin
Loganathan, Madhumathi
Bielak, Dominika
Sung, Molly M. H.
Tam, Ying K.
Krammer, Florian
McMahon, Meagan
author_facet Pardi, Norbert
Carreño, Juan Manuel
O’Dell, George
Tan, Jessica
Bajusz, Csaba
Muramatsu, Hiromi
Rijnink, Willemijn
Strohmeier, Shirin
Loganathan, Madhumathi
Bielak, Dominika
Sung, Molly M. H.
Tam, Ying K.
Krammer, Florian
McMahon, Meagan
author_sort Pardi, Norbert
collection PubMed
description Messenger RNA (mRNA) vaccines represent a new, effective vaccine platform with high capacity for rapid development. Generation of a universal influenza virus vaccine with the potential to elicit long-lasting, broadly cross-reactive immune responses is a necessity for reducing influenza-associated morbidity and mortality. Here we focus on the development of a universal influenza B virus vaccine based on the lipid nanoparticle-encapsulated nucleoside-modified mRNA (mRNA-LNP) platform. We evaluate vaccine candidates based on different target antigens that afford protection against challenge with ancestral and recent influenza B viruses from both antigenic lineages. A pentavalent vaccine combining all tested antigens protects mice from morbidity at a very low dose of 50 ng per antigen after a single vaccination. These findings support the further advancement of nucleoside-modified mRNA-LNPs expressing multiple conserved antigens as universal influenza virus vaccine candidates.
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spelling pubmed-93629762022-08-10 Development of a pentavalent broadly protective nucleoside-modified mRNA vaccine against influenza B viruses Pardi, Norbert Carreño, Juan Manuel O’Dell, George Tan, Jessica Bajusz, Csaba Muramatsu, Hiromi Rijnink, Willemijn Strohmeier, Shirin Loganathan, Madhumathi Bielak, Dominika Sung, Molly M. H. Tam, Ying K. Krammer, Florian McMahon, Meagan Nat Commun Article Messenger RNA (mRNA) vaccines represent a new, effective vaccine platform with high capacity for rapid development. Generation of a universal influenza virus vaccine with the potential to elicit long-lasting, broadly cross-reactive immune responses is a necessity for reducing influenza-associated morbidity and mortality. Here we focus on the development of a universal influenza B virus vaccine based on the lipid nanoparticle-encapsulated nucleoside-modified mRNA (mRNA-LNP) platform. We evaluate vaccine candidates based on different target antigens that afford protection against challenge with ancestral and recent influenza B viruses from both antigenic lineages. A pentavalent vaccine combining all tested antigens protects mice from morbidity at a very low dose of 50 ng per antigen after a single vaccination. These findings support the further advancement of nucleoside-modified mRNA-LNPs expressing multiple conserved antigens as universal influenza virus vaccine candidates. Nature Publishing Group UK 2022-08-09 /pmc/articles/PMC9362976/ /pubmed/35945226 http://dx.doi.org/10.1038/s41467-022-32149-8 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 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
Pardi, Norbert
Carreño, Juan Manuel
O’Dell, George
Tan, Jessica
Bajusz, Csaba
Muramatsu, Hiromi
Rijnink, Willemijn
Strohmeier, Shirin
Loganathan, Madhumathi
Bielak, Dominika
Sung, Molly M. H.
Tam, Ying K.
Krammer, Florian
McMahon, Meagan
Development of a pentavalent broadly protective nucleoside-modified mRNA vaccine against influenza B viruses
title Development of a pentavalent broadly protective nucleoside-modified mRNA vaccine against influenza B viruses
title_full Development of a pentavalent broadly protective nucleoside-modified mRNA vaccine against influenza B viruses
title_fullStr Development of a pentavalent broadly protective nucleoside-modified mRNA vaccine against influenza B viruses
title_full_unstemmed Development of a pentavalent broadly protective nucleoside-modified mRNA vaccine against influenza B viruses
title_short Development of a pentavalent broadly protective nucleoside-modified mRNA vaccine against influenza B viruses
title_sort development of a pentavalent broadly protective nucleoside-modified mrna vaccine against influenza b viruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362976/
https://www.ncbi.nlm.nih.gov/pubmed/35945226
http://dx.doi.org/10.1038/s41467-022-32149-8
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