Publication:
Immunological features beyond CD4/CD8 ratio values in older individuals.

dc.contributor.authorGarrido-Rodríguez, Vanesa
dc.contributor.authorHerrero-Fernández, Inés
dc.contributor.authorCastro, María José
dc.contributor.authorCastillo, Ana
dc.contributor.authorRosado-Sánchez, Isaac
dc.contributor.authorGalvá, María Isabel
dc.contributor.authorRamos, Raquel
dc.contributor.authorOlivas-Martínez, Israel
dc.contributor.authorBulnes-Ramos, Ángel
dc.contributor.authorCañizares, Julio
dc.contributor.authorLeal, Manuel
dc.contributor.authorPacheco, Yolanda María
dc.date.accessioned2023-02-09T11:38:55Z
dc.date.available2023-02-09T11:38:55Z
dc.date.issued2021-05-26
dc.description.abstractThe 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 (65 years old) who were classified as having lower (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.
dc.identifier.doi10.18632/aging.203109
dc.identifier.essn1945-4589
dc.identifier.pmcPMC8202849
dc.identifier.pmid34038386
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202849/pdf
dc.identifier.unpaywallURLhttps://www.aging-us.com/article/203109/pdf
dc.identifier.urihttp://hdl.handle.net/10668/17835
dc.issue.number10
dc.journal.titleAging
dc.journal.titleabbreviationAging (Albany NY)
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number13443-13459
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCD4/CD8 T-cell ratio
dc.subjectTREC
dc.subjectTreg
dc.subjectinflammation
dc.subjectthymic output
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshCD4-Positive T-Lymphocytes
dc.subject.meshCD8-Positive T-Lymphocytes
dc.subject.meshCTLA-4 Antigen
dc.subject.meshCell Compartmentation
dc.subject.meshComorbidity
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshInflammation
dc.subject.meshLymphocyte Subsets
dc.subject.meshMale
dc.subject.meshPhenotype
dc.subject.meshT-Lymphocytes, Regulatory
dc.subject.meshThymus Gland
dc.titleImmunological features beyond CD4/CD8 ratio values in older individuals.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number13
dspace.entity.typePublication

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