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OVX836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza A subtypes
Inactivated influenza vaccines (IIVs) lack broad efficacy. Cellular immunity to a conserved internal antigen, the nucleoprotein (NP), has been correlated to protection against pandemic and seasonal influenza and thus could have the potential to broaden vaccine efficacy. We developed OVX836, a recomb...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344521/ https://www.ncbi.nlm.nih.gov/pubmed/30701093 http://dx.doi.org/10.1038/s41541-019-0098-4 |
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author | Del Campo, Judith Pizzorno, Andres Djebali, Sophia Bouley, Julien Haller, Marjorie Pérez-Vargas, Jimena Lina, Bruno Boivin, Guy Hamelin, Marie-Eve Nicolas, Florence Le Vert, Alexandre Leverrier, Yann Rosa-Calatrava, Manuel Marvel, Jacqueline Hill, Fergal |
author_facet | Del Campo, Judith Pizzorno, Andres Djebali, Sophia Bouley, Julien Haller, Marjorie Pérez-Vargas, Jimena Lina, Bruno Boivin, Guy Hamelin, Marie-Eve Nicolas, Florence Le Vert, Alexandre Leverrier, Yann Rosa-Calatrava, Manuel Marvel, Jacqueline Hill, Fergal |
author_sort | Del Campo, Judith |
collection | PubMed |
description | Inactivated influenza vaccines (IIVs) lack broad efficacy. Cellular immunity to a conserved internal antigen, the nucleoprotein (NP), has been correlated to protection against pandemic and seasonal influenza and thus could have the potential to broaden vaccine efficacy. We developed OVX836, a recombinant protein vaccine based on an oligomerized NP, which shows increased uptake by dendritic cells and immunogenicity compared with NP. Intramuscular immunization in mice with OVX836 induced strong NP-specific CD4+ and CD8+ T-cell systemic responses and established CD8+ tissue memory T cells in the lung parenchyma. Strikingly, OVX836 protected mice against viral challenge with three different influenza A subtypes, isolated several decades apart and induced a reduction in viral load. When co-administered with IIV, OVX836 was even more effective in reducing lung viral load. |
format | Online Article Text |
id | pubmed-6344521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63445212019-01-30 OVX836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza A subtypes Del Campo, Judith Pizzorno, Andres Djebali, Sophia Bouley, Julien Haller, Marjorie Pérez-Vargas, Jimena Lina, Bruno Boivin, Guy Hamelin, Marie-Eve Nicolas, Florence Le Vert, Alexandre Leverrier, Yann Rosa-Calatrava, Manuel Marvel, Jacqueline Hill, Fergal NPJ Vaccines Article Inactivated influenza vaccines (IIVs) lack broad efficacy. Cellular immunity to a conserved internal antigen, the nucleoprotein (NP), has been correlated to protection against pandemic and seasonal influenza and thus could have the potential to broaden vaccine efficacy. We developed OVX836, a recombinant protein vaccine based on an oligomerized NP, which shows increased uptake by dendritic cells and immunogenicity compared with NP. Intramuscular immunization in mice with OVX836 induced strong NP-specific CD4+ and CD8+ T-cell systemic responses and established CD8+ tissue memory T cells in the lung parenchyma. Strikingly, OVX836 protected mice against viral challenge with three different influenza A subtypes, isolated several decades apart and induced a reduction in viral load. When co-administered with IIV, OVX836 was even more effective in reducing lung viral load. Nature Publishing Group UK 2019-01-23 /pmc/articles/PMC6344521/ /pubmed/30701093 http://dx.doi.org/10.1038/s41541-019-0098-4 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Del Campo, Judith Pizzorno, Andres Djebali, Sophia Bouley, Julien Haller, Marjorie Pérez-Vargas, Jimena Lina, Bruno Boivin, Guy Hamelin, Marie-Eve Nicolas, Florence Le Vert, Alexandre Leverrier, Yann Rosa-Calatrava, Manuel Marvel, Jacqueline Hill, Fergal OVX836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza A subtypes |
title | OVX836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza A subtypes |
title_full | OVX836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza A subtypes |
title_fullStr | OVX836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza A subtypes |
title_full_unstemmed | OVX836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza A subtypes |
title_short | OVX836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza A subtypes |
title_sort | ovx836 a recombinant nucleoprotein vaccine inducing cellular responses and protective efficacy against multiple influenza a subtypes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344521/ https://www.ncbi.nlm.nih.gov/pubmed/30701093 http://dx.doi.org/10.1038/s41541-019-0098-4 |
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