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PapMV nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine

BACKGROUND: Trivalent inactivated flu vaccines (TIV) are currently the best means to prevent influenza infections. However, the protection provided by TIV is partial (about 50%) and it is needed to improve the efficacy of protection. Since the respiratory tract is the main site of influenza replicat...

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Autores principales: Rioux, Gervais, Mathieu, Claudia, Russell, Alexis, Bolduc, Marilène, Laliberté-Gagné, Marie-Eve, Savard, Pierre, Leclerc, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022981/
https://www.ncbi.nlm.nih.gov/pubmed/24885884
http://dx.doi.org/10.1186/1477-3155-12-19
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author Rioux, Gervais
Mathieu, Claudia
Russell, Alexis
Bolduc, Marilène
Laliberté-Gagné, Marie-Eve
Savard, Pierre
Leclerc, Denis
author_facet Rioux, Gervais
Mathieu, Claudia
Russell, Alexis
Bolduc, Marilène
Laliberté-Gagné, Marie-Eve
Savard, Pierre
Leclerc, Denis
author_sort Rioux, Gervais
collection PubMed
description BACKGROUND: Trivalent inactivated flu vaccines (TIV) are currently the best means to prevent influenza infections. However, the protection provided by TIV is partial (about 50%) and it is needed to improve the efficacy of protection. Since the respiratory tract is the main site of influenza replications, a vaccine that triggers mucosal immunity in this region can potentially improve protection against this disease. Recently, PapMV nanoparticles used as an adjuvant in a formulation with TIV administered by the subcutaneous route have shown improving the immune response directed to the TIV and protection against an influenza challenge. FINDINGS: In the present study, we showed that intranasal instillation with a formulation containing TIV and PapMV nanoparticles significantly increase the amount of IgG, IgG2a and IgA in lungs of vaccinated mice as compared to mice that received TIV only. Instillation with the adjuvanted formulation leads to a more robust protection against an influenza infection with a strain that is lethal to mice vaccinated with the TIV. CONCLUSIONS: We demonstrate for the first time that PapMV nanoparticles are an effective and potent mucosal adjuvant for vaccination.
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spelling pubmed-40229812014-05-17 PapMV nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine Rioux, Gervais Mathieu, Claudia Russell, Alexis Bolduc, Marilène Laliberté-Gagné, Marie-Eve Savard, Pierre Leclerc, Denis J Nanobiotechnology Short Communication BACKGROUND: Trivalent inactivated flu vaccines (TIV) are currently the best means to prevent influenza infections. However, the protection provided by TIV is partial (about 50%) and it is needed to improve the efficacy of protection. Since the respiratory tract is the main site of influenza replications, a vaccine that triggers mucosal immunity in this region can potentially improve protection against this disease. Recently, PapMV nanoparticles used as an adjuvant in a formulation with TIV administered by the subcutaneous route have shown improving the immune response directed to the TIV and protection against an influenza challenge. FINDINGS: In the present study, we showed that intranasal instillation with a formulation containing TIV and PapMV nanoparticles significantly increase the amount of IgG, IgG2a and IgA in lungs of vaccinated mice as compared to mice that received TIV only. Instillation with the adjuvanted formulation leads to a more robust protection against an influenza infection with a strain that is lethal to mice vaccinated with the TIV. CONCLUSIONS: We demonstrate for the first time that PapMV nanoparticles are an effective and potent mucosal adjuvant for vaccination. BioMed Central 2014-05-03 /pmc/articles/PMC4022981/ /pubmed/24885884 http://dx.doi.org/10.1186/1477-3155-12-19 Text en Copyright © 2014 Rioux et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Communication
Rioux, Gervais
Mathieu, Claudia
Russell, Alexis
Bolduc, Marilène
Laliberté-Gagné, Marie-Eve
Savard, Pierre
Leclerc, Denis
PapMV nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine
title PapMV nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine
title_full PapMV nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine
title_fullStr PapMV nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine
title_full_unstemmed PapMV nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine
title_short PapMV nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine
title_sort papmv nanoparticles improve mucosal immune responses to the trivalent inactivated flu vaccine
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022981/
https://www.ncbi.nlm.nih.gov/pubmed/24885884
http://dx.doi.org/10.1186/1477-3155-12-19
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