Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1782316485005279232 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4022981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT riouxgervais papmvnanoparticlesimprovemucosalimmuneresponsestothetrivalentinactivatedfluvaccine AT mathieuclaudia papmvnanoparticlesimprovemucosalimmuneresponsestothetrivalentinactivatedfluvaccine AT russellalexis papmvnanoparticlesimprovemucosalimmuneresponsestothetrivalentinactivatedfluvaccine AT bolducmarilene papmvnanoparticlesimprovemucosalimmuneresponsestothetrivalentinactivatedfluvaccine AT lalibertegagnemarieeve papmvnanoparticlesimprovemucosalimmuneresponsestothetrivalentinactivatedfluvaccine AT savardpierre papmvnanoparticlesimprovemucosalimmuneresponsestothetrivalentinactivatedfluvaccine AT leclercdenis papmvnanoparticlesimprovemucosalimmuneresponsestothetrivalentinactivatedfluvaccine |