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Host Resistance and Immune Responses in Advanced Age

Immunosenescence results in populating immune tissues with less functional T cells, and perhaps B cells dendritic cells, that do not function well and produce more type 2 cytokines and fewer type 1 cytokines. Impaired immunity, distinct from immunosenescence, correlates more with disease burden than...

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Detalles Bibliográficos
Autores principales: Castle, Steven C., Uyemura, Koichi, Fulop, Tamas, Makinodan, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7135540/
https://www.ncbi.nlm.nih.gov/pubmed/17631228
http://dx.doi.org/10.1016/j.cger.2007.03.005
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author Castle, Steven C.
Uyemura, Koichi
Fulop, Tamas
Makinodan, Takashi
author_facet Castle, Steven C.
Uyemura, Koichi
Fulop, Tamas
Makinodan, Takashi
author_sort Castle, Steven C.
collection PubMed
description Immunosenescence results in populating immune tissues with less functional T cells, and perhaps B cells dendritic cells, that do not function well and produce more type 2 cytokines and fewer type 1 cytokines. Impaired immunity, distinct from immunosenescence, correlates more with disease burden than chronologic age. Older adults who have chronic diseases or chronic infections are more susceptible to common infections and have poor vaccine responses. Understanding specific mechanisms and targeting interventions are dependent on research to resolve the relationship between frailty-associated impaired immunity and the role of chronic infection versus immunosenescence in developing impaired immunity.
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spelling pubmed-71355402020-04-08 Host Resistance and Immune Responses in Advanced Age Castle, Steven C. Uyemura, Koichi Fulop, Tamas Makinodan, Takashi Clin Geriatr Med Article Immunosenescence results in populating immune tissues with less functional T cells, and perhaps B cells dendritic cells, that do not function well and produce more type 2 cytokines and fewer type 1 cytokines. Impaired immunity, distinct from immunosenescence, correlates more with disease burden than chronologic age. Older adults who have chronic diseases or chronic infections are more susceptible to common infections and have poor vaccine responses. Understanding specific mechanisms and targeting interventions are dependent on research to resolve the relationship between frailty-associated impaired immunity and the role of chronic infection versus immunosenescence in developing impaired immunity. Published by Elsevier Inc. 2007-08 2007-07-11 /pmc/articles/PMC7135540/ /pubmed/17631228 http://dx.doi.org/10.1016/j.cger.2007.03.005 Text en Copyright © 2007 Published by Elsevier Inc. 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
Castle, Steven C.
Uyemura, Koichi
Fulop, Tamas
Makinodan, Takashi
Host Resistance and Immune Responses in Advanced Age
title Host Resistance and Immune Responses in Advanced Age
title_full Host Resistance and Immune Responses in Advanced Age
title_fullStr Host Resistance and Immune Responses in Advanced Age
title_full_unstemmed Host Resistance and Immune Responses in Advanced Age
title_short Host Resistance and Immune Responses in Advanced Age
title_sort host resistance and immune responses in advanced age
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7135540/
https://www.ncbi.nlm.nih.gov/pubmed/17631228
http://dx.doi.org/10.1016/j.cger.2007.03.005
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