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Adaptive immunity to rhinoviruses: sex and age matter

BACKGROUND: Rhinoviruses (RV) are key triggers in acute asthma exacerbations. Previous studies suggest that men suffer from infectious diseases more frequently and with greater severity than women. Additionally, the immune response to most infections and vaccinations decreases with age. Most immune...

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Autores principales: Carroll , Melanie L, Yerkovich , Stephanie T, Pritchard , Antonia L, Davies , Janet M, Upham, John W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024249/
https://www.ncbi.nlm.nih.gov/pubmed/21194432
http://dx.doi.org/10.1186/1465-9921-11-184
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author Carroll , Melanie L
Yerkovich , Stephanie T
Pritchard , Antonia L
Davies , Janet M
Upham, John W
author_facet Carroll , Melanie L
Yerkovich , Stephanie T
Pritchard , Antonia L
Davies , Janet M
Upham, John W
author_sort Carroll , Melanie L
collection PubMed
description BACKGROUND: Rhinoviruses (RV) are key triggers in acute asthma exacerbations. Previous studies suggest that men suffer from infectious diseases more frequently and with greater severity than women. Additionally, the immune response to most infections and vaccinations decreases with age. Most immune function studies do not account for such differences, therefore the aim of this study was to determine if the immune response to rhinovirus varies with sex or age. METHODS: Blood mononuclear cells were isolated from 63 healthy individuals and grouped by sex and age (≤50 years old and ≥52 years old). Cells were cultured with rhinovirus 16 at a multiplicity of infection of 1. The chemokine IP-10 was measured at 24 h as an index of innate immunity while IFNγ and IL-13 were measured at 5 days as an index of adaptive immunity. RESULTS: Rhinovirus induced IFNγ and IL-13 was significantly higher in ≤50 year old women than in age matched men (p < 0.02 and p < 0.05) and ≥52 year old women (p < 0.02 and p > 0.005). There was no sex or age based difference in rhinovirus induced IP-10 expression. Both IFNγ and IL-13 were negatively correlated with age in women but not in men. CONCLUSIONS: This study suggests that pre-menopausal women have a stronger adaptive immune response to rhinovirus infection than men and older people, though the mechanisms responsible for these differences remain to be determined. Our findings highlight the importance of gender and age balance in clinical studies and in the development of new treatments and vaccines.
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spelling pubmed-30242492011-01-21 Adaptive immunity to rhinoviruses: sex and age matter Carroll , Melanie L Yerkovich , Stephanie T Pritchard , Antonia L Davies , Janet M Upham, John W Respir Res Research BACKGROUND: Rhinoviruses (RV) are key triggers in acute asthma exacerbations. Previous studies suggest that men suffer from infectious diseases more frequently and with greater severity than women. Additionally, the immune response to most infections and vaccinations decreases with age. Most immune function studies do not account for such differences, therefore the aim of this study was to determine if the immune response to rhinovirus varies with sex or age. METHODS: Blood mononuclear cells were isolated from 63 healthy individuals and grouped by sex and age (≤50 years old and ≥52 years old). Cells were cultured with rhinovirus 16 at a multiplicity of infection of 1. The chemokine IP-10 was measured at 24 h as an index of innate immunity while IFNγ and IL-13 were measured at 5 days as an index of adaptive immunity. RESULTS: Rhinovirus induced IFNγ and IL-13 was significantly higher in ≤50 year old women than in age matched men (p < 0.02 and p < 0.05) and ≥52 year old women (p < 0.02 and p > 0.005). There was no sex or age based difference in rhinovirus induced IP-10 expression. Both IFNγ and IL-13 were negatively correlated with age in women but not in men. CONCLUSIONS: This study suggests that pre-menopausal women have a stronger adaptive immune response to rhinovirus infection than men and older people, though the mechanisms responsible for these differences remain to be determined. Our findings highlight the importance of gender and age balance in clinical studies and in the development of new treatments and vaccines. BioMed Central 2010 2010-12-31 /pmc/articles/PMC3024249/ /pubmed/21194432 http://dx.doi.org/10.1186/1465-9921-11-184 Text en Copyright ©2010 Carroll et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Carroll , Melanie L
Yerkovich , Stephanie T
Pritchard , Antonia L
Davies , Janet M
Upham, John W
Adaptive immunity to rhinoviruses: sex and age matter
title Adaptive immunity to rhinoviruses: sex and age matter
title_full Adaptive immunity to rhinoviruses: sex and age matter
title_fullStr Adaptive immunity to rhinoviruses: sex and age matter
title_full_unstemmed Adaptive immunity to rhinoviruses: sex and age matter
title_short Adaptive immunity to rhinoviruses: sex and age matter
title_sort adaptive immunity to rhinoviruses: sex and age matter
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024249/
https://www.ncbi.nlm.nih.gov/pubmed/21194432
http://dx.doi.org/10.1186/1465-9921-11-184
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AT daviesjanetm adaptiveimmunitytorhinovirusessexandagematter
AT uphamjohnw adaptiveimmunitytorhinovirusessexandagematter