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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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