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Age and immunity
Longitudinal studies are defining progressive alterations to the immune system associated with increased mortality in the very elderly. Many of these changes are exacerbated by or even caused by chronic T cell stimulation by persistent antigen, particularly from Cytomegalovirus. The composition of T...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1402324/ https://www.ncbi.nlm.nih.gov/pubmed/16504129 http://dx.doi.org/10.1186/1742-4933-3-2 |
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author | Vasto, Sonya Malavolta, Marco Pawelec, Graham |
author_facet | Vasto, Sonya Malavolta, Marco Pawelec, Graham |
author_sort | Vasto, Sonya |
collection | PubMed |
description | Longitudinal studies are defining progressive alterations to the immune system associated with increased mortality in the very elderly. Many of these changes are exacerbated by or even caused by chronic T cell stimulation by persistent antigen, particularly from Cytomegalovirus. The composition of T cell subsets, their functional integrity and representation in the repertoire are all markedly influenced by age and by CMV. How these findings relate to epidemiological, functional, genetic, genomic and proteomic studies of human T cell immunosenescence was the subject of intense debate at an international conference held just before Christmas 2005 in the Black Forest. |
format | Text |
id | pubmed-1402324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-14023242006-03-16 Age and immunity Vasto, Sonya Malavolta, Marco Pawelec, Graham Immun Ageing Short Report Longitudinal studies are defining progressive alterations to the immune system associated with increased mortality in the very elderly. Many of these changes are exacerbated by or even caused by chronic T cell stimulation by persistent antigen, particularly from Cytomegalovirus. The composition of T cell subsets, their functional integrity and representation in the repertoire are all markedly influenced by age and by CMV. How these findings relate to epidemiological, functional, genetic, genomic and proteomic studies of human T cell immunosenescence was the subject of intense debate at an international conference held just before Christmas 2005 in the Black Forest. BioMed Central 2006-02-24 /pmc/articles/PMC1402324/ /pubmed/16504129 http://dx.doi.org/10.1186/1742-4933-3-2 Text en Copyright © 2006 Vasto 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 cited. |
spellingShingle | Short Report Vasto, Sonya Malavolta, Marco Pawelec, Graham Age and immunity |
title | Age and immunity |
title_full | Age and immunity |
title_fullStr | Age and immunity |
title_full_unstemmed | Age and immunity |
title_short | Age and immunity |
title_sort | age and immunity |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1402324/ https://www.ncbi.nlm.nih.gov/pubmed/16504129 http://dx.doi.org/10.1186/1742-4933-3-2 |
work_keys_str_mv | AT vastosonya ageandimmunity AT malavoltamarco ageandimmunity AT pawelecgraham ageandimmunity |