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Immunological features beyond CD4/CD8 ratio values in older individuals
The CD4/CD8 T-cell ratio is emerging as a relevant marker of evolution for many pathologies and therapies. We aimed to explore immunological features beyond CD4/CD8 ratio values in older subjects (>65 years old) who were classified as having lower (<1.4), intermediate (1.4-2), or higher (>2...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202849/ https://www.ncbi.nlm.nih.gov/pubmed/34038386 http://dx.doi.org/10.18632/aging.203109 |
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author | Garrido-Rodríguez, Vanesa Herrero-Fernández, Inés Castro, María José Castillo, Ana Rosado-Sánchez, Isaac Galvá, María Isabel Ramos, Raquel Olivas-Martínez, Israel Bulnes-Ramos, Ángel Cañizares, Julio Leal, Manuel Pacheco, Yolanda María |
author_facet | Garrido-Rodríguez, Vanesa Herrero-Fernández, Inés Castro, María José Castillo, Ana Rosado-Sánchez, Isaac Galvá, María Isabel Ramos, Raquel Olivas-Martínez, Israel Bulnes-Ramos, Ángel Cañizares, Julio Leal, Manuel Pacheco, Yolanda María |
author_sort | Garrido-Rodríguez, Vanesa |
collection | PubMed |
description | The CD4/CD8 T-cell ratio is emerging as a relevant marker of evolution for many pathologies and therapies. We aimed to explore immunological features beyond CD4/CD8 ratio values in older subjects (>65 years old) who were classified as having lower (<1.4), intermediate (1.4-2), or higher (>2) ratio values. The lower group showed a lower thymic output (sj/β-TREC ratio) and frequency of naïve T-cells, concomitant with increased mature T-cells. In these subjects, the CD4 T-cell subset was enriched in CD95+ but depleted of CD98+ cells. The regulatory T-cell (Treg) compartment was enriched in CTLA-4+ cells. The CD8 T-cell pool exhibited increased frequencies of CD95+ cells but decreased frequencies of integrin-β7+ cells. Interestingly, in the intermediate group, the CD4 pool showed greater differences than the CD8 pool, mostly for cellular senescence. Regarding inflammation, only hsCRP was elevated in the lower group; however, negative correlations between the CD4/CD8 ratio and β2-microglobulin and sCD163 were detected. These subjects displayed trends of more comorbidities and less independence in daily activities. Altogether, our data reveal different thymic output and immune profiles for T-cells across CD4/CD8 ratio values that can define immune capabilities, affecting health status in older individuals. Thus, the CD4/CD8 ratio may be used as an integrative marker of biological age. |
format | Online Article Text |
id | pubmed-8202849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-82028492021-06-15 Immunological features beyond CD4/CD8 ratio values in older individuals Garrido-Rodríguez, Vanesa Herrero-Fernández, Inés Castro, María José Castillo, Ana Rosado-Sánchez, Isaac Galvá, María Isabel Ramos, Raquel Olivas-Martínez, Israel Bulnes-Ramos, Ángel Cañizares, Julio Leal, Manuel Pacheco, Yolanda María Aging (Albany NY) Research Paper The CD4/CD8 T-cell ratio is emerging as a relevant marker of evolution for many pathologies and therapies. We aimed to explore immunological features beyond CD4/CD8 ratio values in older subjects (>65 years old) who were classified as having lower (<1.4), intermediate (1.4-2), or higher (>2) ratio values. The lower group showed a lower thymic output (sj/β-TREC ratio) and frequency of naïve T-cells, concomitant with increased mature T-cells. In these subjects, the CD4 T-cell subset was enriched in CD95+ but depleted of CD98+ cells. The regulatory T-cell (Treg) compartment was enriched in CTLA-4+ cells. The CD8 T-cell pool exhibited increased frequencies of CD95+ cells but decreased frequencies of integrin-β7+ cells. Interestingly, in the intermediate group, the CD4 pool showed greater differences than the CD8 pool, mostly for cellular senescence. Regarding inflammation, only hsCRP was elevated in the lower group; however, negative correlations between the CD4/CD8 ratio and β2-microglobulin and sCD163 were detected. These subjects displayed trends of more comorbidities and less independence in daily activities. Altogether, our data reveal different thymic output and immune profiles for T-cells across CD4/CD8 ratio values that can define immune capabilities, affecting health status in older individuals. Thus, the CD4/CD8 ratio may be used as an integrative marker of biological age. Impact Journals 2021-05-26 /pmc/articles/PMC8202849/ /pubmed/34038386 http://dx.doi.org/10.18632/aging.203109 Text en Copyright: © 2021 Garrido-Rodríguez et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Garrido-Rodríguez, Vanesa Herrero-Fernández, Inés Castro, María José Castillo, Ana Rosado-Sánchez, Isaac Galvá, María Isabel Ramos, Raquel Olivas-Martínez, Israel Bulnes-Ramos, Ángel Cañizares, Julio Leal, Manuel Pacheco, Yolanda María Immunological features beyond CD4/CD8 ratio values in older individuals |
title | Immunological features beyond CD4/CD8 ratio values in older individuals |
title_full | Immunological features beyond CD4/CD8 ratio values in older individuals |
title_fullStr | Immunological features beyond CD4/CD8 ratio values in older individuals |
title_full_unstemmed | Immunological features beyond CD4/CD8 ratio values in older individuals |
title_short | Immunological features beyond CD4/CD8 ratio values in older individuals |
title_sort | immunological features beyond cd4/cd8 ratio values in older individuals |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202849/ https://www.ncbi.nlm.nih.gov/pubmed/34038386 http://dx.doi.org/10.18632/aging.203109 |
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