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Immunity and age: living in the past?

Increasing age is associated with a decreasing ability to mediate effective immune responses to newly encountered antigens. It is generally believed that this reflects the age-associated decline in the number, repertoire and function of available naive T cells. Here, we propose that naive T cells be...

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Detalles Bibliográficos
Autores principales: Woodland, David L., Blackman, Marcia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185388/
https://www.ncbi.nlm.nih.gov/pubmed/16731040
http://dx.doi.org/10.1016/j.it.2006.05.002
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author Woodland, David L.
Blackman, Marcia A.
author_facet Woodland, David L.
Blackman, Marcia A.
author_sort Woodland, David L.
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description Increasing age is associated with a decreasing ability to mediate effective immune responses to newly encountered antigens. It is generally believed that this reflects the age-associated decline in the number, repertoire and function of available naive T cells. Here, we propose that naive T cells become increasingly irrelevant to the immune system, and that responses to newly encountered antigens are progressively dominated by cross-reactive memory T cells as the individual ages. In addition, we propose that the majority, if not all, of the response to newly encountered antigens in the elderly is mediated by cross-reactive memory T cells. This predicts highly stochastic responses to new infections that should vary between individuals, and has important implications for vaccination strategies in the elderly.
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spelling pubmed-71853882020-04-28 Immunity and age: living in the past? Woodland, David L. Blackman, Marcia A. Trends Immunol Article Increasing age is associated with a decreasing ability to mediate effective immune responses to newly encountered antigens. It is generally believed that this reflects the age-associated decline in the number, repertoire and function of available naive T cells. Here, we propose that naive T cells become increasingly irrelevant to the immune system, and that responses to newly encountered antigens are progressively dominated by cross-reactive memory T cells as the individual ages. In addition, we propose that the majority, if not all, of the response to newly encountered antigens in the elderly is mediated by cross-reactive memory T cells. This predicts highly stochastic responses to new infections that should vary between individuals, and has important implications for vaccination strategies in the elderly. Elsevier Ltd. 2006-07 2006-05-30 /pmc/articles/PMC7185388/ /pubmed/16731040 http://dx.doi.org/10.1016/j.it.2006.05.002 Text en Copyright © 2006 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Woodland, David L.
Blackman, Marcia A.
Immunity and age: living in the past?
title Immunity and age: living in the past?
title_full Immunity and age: living in the past?
title_fullStr Immunity and age: living in the past?
title_full_unstemmed Immunity and age: living in the past?
title_short Immunity and age: living in the past?
title_sort immunity and age: living in the past?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185388/
https://www.ncbi.nlm.nih.gov/pubmed/16731040
http://dx.doi.org/10.1016/j.it.2006.05.002
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