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The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study
The Swedish OCTO and NONA immune longitudinal studies were able to identify and confirm an immune risk profile (IRP) predictive of an increased 2-year mortality in very old individuals, 86–94 years of age. The IRP, was associated with persistent cytomegalovirus infection and characterized by inverte...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636392/ https://www.ncbi.nlm.nih.gov/pubmed/22415616 http://dx.doi.org/10.1007/s11357-012-9400-3 |
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author | Strindhall, J. Skog, M. Ernerudh, J. Bengner, M. Löfgren, S. Matussek, A. Nilsson, B. O. Wikby, A. |
author_facet | Strindhall, J. Skog, M. Ernerudh, J. Bengner, M. Löfgren, S. Matussek, A. Nilsson, B. O. Wikby, A. |
author_sort | Strindhall, J. |
collection | PubMed |
description | The Swedish OCTO and NONA immune longitudinal studies were able to identify and confirm an immune risk profile (IRP) predictive of an increased 2-year mortality in very old individuals, 86–94 years of age. The IRP, was associated with persistent cytomegalovirus infection and characterized by inverted CD4/CD8 ratio and related to expansion of terminally differentiated effector memory T cells (TEMRA phenotype). In the present HEXA immune longitudinal study, we have examined a younger group of elderly individuals (n = 424, 66 years of age) in a population-based sample in the community of Jönköping, Sweden, to examine the relevance of findings previously demonstrated in the very old. Immunological monitoring that was conducted included T cell subsets and CMV-IgG and CMV-IgM serology. The result showed a prevalence of 15 % of individuals with an inverted CD4/CD8 ratio, which was associated with seropositivity to cytomegalovirus and increases in the level of TEMRA cells. The proportion of individuals with an inverted CD4/CD8 ratio was significantly higher in men whereas the numbers of CD3+CD4+ cells were significantly higher in women. In conclusion, these findings are very similar to those previously found by us in the Swedish longitudinal studies, suggesting that an immune profile previously identified in the very old also exists in the present sample of hexagenerians. Therefore, it will be important to examine clinical parameters, including morbidity and mortality, to assess whether the immune profile also is a risk profile associated with higher mortality in this sample of hexagenerians. |
format | Online Article Text |
id | pubmed-3636392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-36363922013-04-29 The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study Strindhall, J. Skog, M. Ernerudh, J. Bengner, M. Löfgren, S. Matussek, A. Nilsson, B. O. Wikby, A. Age (Dordr) Article The Swedish OCTO and NONA immune longitudinal studies were able to identify and confirm an immune risk profile (IRP) predictive of an increased 2-year mortality in very old individuals, 86–94 years of age. The IRP, was associated with persistent cytomegalovirus infection and characterized by inverted CD4/CD8 ratio and related to expansion of terminally differentiated effector memory T cells (TEMRA phenotype). In the present HEXA immune longitudinal study, we have examined a younger group of elderly individuals (n = 424, 66 years of age) in a population-based sample in the community of Jönköping, Sweden, to examine the relevance of findings previously demonstrated in the very old. Immunological monitoring that was conducted included T cell subsets and CMV-IgG and CMV-IgM serology. The result showed a prevalence of 15 % of individuals with an inverted CD4/CD8 ratio, which was associated with seropositivity to cytomegalovirus and increases in the level of TEMRA cells. The proportion of individuals with an inverted CD4/CD8 ratio was significantly higher in men whereas the numbers of CD3+CD4+ cells were significantly higher in women. In conclusion, these findings are very similar to those previously found by us in the Swedish longitudinal studies, suggesting that an immune profile previously identified in the very old also exists in the present sample of hexagenerians. Therefore, it will be important to examine clinical parameters, including morbidity and mortality, to assess whether the immune profile also is a risk profile associated with higher mortality in this sample of hexagenerians. Springer Netherlands 2012-03-14 2013-06 /pmc/articles/PMC3636392/ /pubmed/22415616 http://dx.doi.org/10.1007/s11357-012-9400-3 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Article Strindhall, J. Skog, M. Ernerudh, J. Bengner, M. Löfgren, S. Matussek, A. Nilsson, B. O. Wikby, A. The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study |
title | The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study |
title_full | The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study |
title_fullStr | The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study |
title_full_unstemmed | The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study |
title_short | The inverted CD4/CD8 ratio and associated parameters in 66-year-old individuals: the Swedish HEXA immune study |
title_sort | inverted cd4/cd8 ratio and associated parameters in 66-year-old individuals: the swedish hexa immune study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636392/ https://www.ncbi.nlm.nih.gov/pubmed/22415616 http://dx.doi.org/10.1007/s11357-012-9400-3 |
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