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Immunosenescence and human vaccine immune responses

The age-related dysregulation and decline of the immune system—collectively termed “immunosenescence”—has been generally associated with an increased susceptibility to infectious pathogens and poor vaccine responses in older adults. While numerous studies have reported on the clinical outcomes of in...

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Autores principales: Crooke, Stephen N., Ovsyannikova, Inna G., Poland, Gregory A., Kennedy, Richard B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743147/
https://www.ncbi.nlm.nih.gov/pubmed/31528180
http://dx.doi.org/10.1186/s12979-019-0164-9
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author Crooke, Stephen N.
Ovsyannikova, Inna G.
Poland, Gregory A.
Kennedy, Richard B.
author_facet Crooke, Stephen N.
Ovsyannikova, Inna G.
Poland, Gregory A.
Kennedy, Richard B.
author_sort Crooke, Stephen N.
collection PubMed
description The age-related dysregulation and decline of the immune system—collectively termed “immunosenescence”—has been generally associated with an increased susceptibility to infectious pathogens and poor vaccine responses in older adults. While numerous studies have reported on the clinical outcomes of infected or vaccinated individuals, our understanding of the mechanisms governing the onset of immunosenescence and its effects on adaptive immunity remains incomplete. Age-dependent differences in T and B lymphocyte populations and functions have been well-defined, yet studies that demonstrate direct associations between immune cell function and clinical outcomes in older individuals are lacking. Despite these knowledge gaps, research has progressed in the development of vaccine and adjuvant formulations tailored for older adults in order to boost protective immunity and overcome immunosenescence. In this review, we will discuss the development of vaccines for older adults in light of our current understanding—or lack thereof—of the aging immune system. We highlight the functional changes that are known to occur in the adaptive immune system with age, followed by a discussion of current, clinically relevant pathogens that disproportionately affect older adults and are the central focus of vaccine research efforts for the aging population. We conclude with an outlook on personalized vaccine development for older adults and areas in need of further study in order to improve our fundamental understanding of adaptive immunosenescence.
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spelling pubmed-67431472019-09-16 Immunosenescence and human vaccine immune responses Crooke, Stephen N. Ovsyannikova, Inna G. Poland, Gregory A. Kennedy, Richard B. Immun Ageing Review The age-related dysregulation and decline of the immune system—collectively termed “immunosenescence”—has been generally associated with an increased susceptibility to infectious pathogens and poor vaccine responses in older adults. While numerous studies have reported on the clinical outcomes of infected or vaccinated individuals, our understanding of the mechanisms governing the onset of immunosenescence and its effects on adaptive immunity remains incomplete. Age-dependent differences in T and B lymphocyte populations and functions have been well-defined, yet studies that demonstrate direct associations between immune cell function and clinical outcomes in older individuals are lacking. Despite these knowledge gaps, research has progressed in the development of vaccine and adjuvant formulations tailored for older adults in order to boost protective immunity and overcome immunosenescence. In this review, we will discuss the development of vaccines for older adults in light of our current understanding—or lack thereof—of the aging immune system. We highlight the functional changes that are known to occur in the adaptive immune system with age, followed by a discussion of current, clinically relevant pathogens that disproportionately affect older adults and are the central focus of vaccine research efforts for the aging population. We conclude with an outlook on personalized vaccine development for older adults and areas in need of further study in order to improve our fundamental understanding of adaptive immunosenescence. BioMed Central 2019-09-13 /pmc/articles/PMC6743147/ /pubmed/31528180 http://dx.doi.org/10.1186/s12979-019-0164-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 Review
Crooke, Stephen N.
Ovsyannikova, Inna G.
Poland, Gregory A.
Kennedy, Richard B.
Immunosenescence and human vaccine immune responses
title Immunosenescence and human vaccine immune responses
title_full Immunosenescence and human vaccine immune responses
title_fullStr Immunosenescence and human vaccine immune responses
title_full_unstemmed Immunosenescence and human vaccine immune responses
title_short Immunosenescence and human vaccine immune responses
title_sort immunosenescence and human vaccine immune responses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743147/
https://www.ncbi.nlm.nih.gov/pubmed/31528180
http://dx.doi.org/10.1186/s12979-019-0164-9
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