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Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic

BACKGROUND: Previous exposures to flu and subsequent immune responses may impact on 2009/2010 pandemic flu vaccine responses and clinical symptoms upon infection with the 2009 pandemic H1N1 influenza strain. Qualitative and quantitative differences in humoral and cellular immune responses associated...

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Autores principales: Magalhaes, Isabelle, Eriksson, Mikael, Linde, Charlotte, Muhammad, Rashid, Rane, Lalit, Ambati, Aditya, Axelsson-Robertson, Rebecca, Khalaj, Bahareh, Alvarez-Corrales, Nancy, Lapini, Giulia, Montomoli, Emanuele, Linde, Annika, Pedersen, Nancy L, Maeurer, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067073/
https://www.ncbi.nlm.nih.gov/pubmed/24916787
http://dx.doi.org/10.1186/1471-2334-14-319
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author Magalhaes, Isabelle
Eriksson, Mikael
Linde, Charlotte
Muhammad, Rashid
Rane, Lalit
Ambati, Aditya
Axelsson-Robertson, Rebecca
Khalaj, Bahareh
Alvarez-Corrales, Nancy
Lapini, Giulia
Montomoli, Emanuele
Linde, Annika
Pedersen, Nancy L
Maeurer, Markus
author_facet Magalhaes, Isabelle
Eriksson, Mikael
Linde, Charlotte
Muhammad, Rashid
Rane, Lalit
Ambati, Aditya
Axelsson-Robertson, Rebecca
Khalaj, Bahareh
Alvarez-Corrales, Nancy
Lapini, Giulia
Montomoli, Emanuele
Linde, Annika
Pedersen, Nancy L
Maeurer, Markus
author_sort Magalhaes, Isabelle
collection PubMed
description BACKGROUND: Previous exposures to flu and subsequent immune responses may impact on 2009/2010 pandemic flu vaccine responses and clinical symptoms upon infection with the 2009 pandemic H1N1 influenza strain. Qualitative and quantitative differences in humoral and cellular immune responses associated with the flu vaccination in 2009/2010 (pandemic H1N1 vaccine) and natural infection have not yet been described in detail. We designed a longitudinal study to examine influenza- (flu-) specific immune responses and the association between pre-existing flu responses, symptoms of influenza-like illness (ILI), impact of pandemic flu infection, and pandemic flu vaccination in a cohort of 2,040 individuals in Sweden in 2009–2010. METHODS: Cellular flu-specific immune responses were assessed by whole-blood antigen stimulation assay, and humoral responses by a single radial hemolysis test. RESULTS: Previous seasonal flu vaccination was associated with significantly lower flu-specific IFN-γ responses (using a whole-blood assay) at study entry. Pandemic flu vaccination induced long-lived T-cell responses (measured by IFN-γ production) to influenza A strains, influenza B strains, and the matrix (M1) antigen. In contrast, individuals with pandemic flu infection (PCR positive) exhibited increased flu-specific T-cell responses shortly after onset of ILI symptoms but the immune response decreased after the flu season (spring 2010). We identified non-pandemic-flu vaccinated participants without ILI symptoms who showed an IFN-γ production profile similar to pandemic-flu infected participants, suggesting exposure without experiencing clinical symptoms. CONCLUSIONS: Strong and long-lived flu-M1 specific immune responses, defined by IFN-γ production, in individuals after vaccination suggest that M1-responses may contribute to protective cellular immune responses. Silent flu infections appeared to be frequent in 2009/2010. The pandemic flu vaccine induced qualitatively and quantitatively different humoral and cellular immune responses as compared to infection with the 2009 H1N1 pandemic H1N1 influenza strain.
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spelling pubmed-40670732014-06-24 Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic Magalhaes, Isabelle Eriksson, Mikael Linde, Charlotte Muhammad, Rashid Rane, Lalit Ambati, Aditya Axelsson-Robertson, Rebecca Khalaj, Bahareh Alvarez-Corrales, Nancy Lapini, Giulia Montomoli, Emanuele Linde, Annika Pedersen, Nancy L Maeurer, Markus BMC Infect Dis Research Article BACKGROUND: Previous exposures to flu and subsequent immune responses may impact on 2009/2010 pandemic flu vaccine responses and clinical symptoms upon infection with the 2009 pandemic H1N1 influenza strain. Qualitative and quantitative differences in humoral and cellular immune responses associated with the flu vaccination in 2009/2010 (pandemic H1N1 vaccine) and natural infection have not yet been described in detail. We designed a longitudinal study to examine influenza- (flu-) specific immune responses and the association between pre-existing flu responses, symptoms of influenza-like illness (ILI), impact of pandemic flu infection, and pandemic flu vaccination in a cohort of 2,040 individuals in Sweden in 2009–2010. METHODS: Cellular flu-specific immune responses were assessed by whole-blood antigen stimulation assay, and humoral responses by a single radial hemolysis test. RESULTS: Previous seasonal flu vaccination was associated with significantly lower flu-specific IFN-γ responses (using a whole-blood assay) at study entry. Pandemic flu vaccination induced long-lived T-cell responses (measured by IFN-γ production) to influenza A strains, influenza B strains, and the matrix (M1) antigen. In contrast, individuals with pandemic flu infection (PCR positive) exhibited increased flu-specific T-cell responses shortly after onset of ILI symptoms but the immune response decreased after the flu season (spring 2010). We identified non-pandemic-flu vaccinated participants without ILI symptoms who showed an IFN-γ production profile similar to pandemic-flu infected participants, suggesting exposure without experiencing clinical symptoms. CONCLUSIONS: Strong and long-lived flu-M1 specific immune responses, defined by IFN-γ production, in individuals after vaccination suggest that M1-responses may contribute to protective cellular immune responses. Silent flu infections appeared to be frequent in 2009/2010. The pandemic flu vaccine induced qualitatively and quantitatively different humoral and cellular immune responses as compared to infection with the 2009 H1N1 pandemic H1N1 influenza strain. BioMed Central 2014-06-11 /pmc/articles/PMC4067073/ /pubmed/24916787 http://dx.doi.org/10.1186/1471-2334-14-319 Text en Copyright © 2014 Magalhaes et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), 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 Research Article
Magalhaes, Isabelle
Eriksson, Mikael
Linde, Charlotte
Muhammad, Rashid
Rane, Lalit
Ambati, Aditya
Axelsson-Robertson, Rebecca
Khalaj, Bahareh
Alvarez-Corrales, Nancy
Lapini, Giulia
Montomoli, Emanuele
Linde, Annika
Pedersen, Nancy L
Maeurer, Markus
Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic
title Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic
title_full Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic
title_fullStr Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic
title_full_unstemmed Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic
title_short Difference in immune response in vaccinated and unvaccinated Swedish individuals after the 2009 influenza pandemic
title_sort difference in immune response in vaccinated and unvaccinated swedish individuals after the 2009 influenza pandemic
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067073/
https://www.ncbi.nlm.nih.gov/pubmed/24916787
http://dx.doi.org/10.1186/1471-2334-14-319
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