Biological age and immunosenescence in Colombian centenarians

Biological aging and immunosenescence are central to longevity, yet their interplay in centenarians remains unclear. We conducted a cross-sectional study in 160 Colombian centenarians to examine associations between biological age (PhenoAge), immunosenescence and age-related clinical variables. Cytokine profiling (n = 114) and lymphocyte immunophenotyping (n = 42) were assessed. It was observed that better QoL and well-being were significantly associated with lower biological age, while depressive symptoms, prior tobacco use, elevated levels of RANTES and G-CSF as well as a distinct CD8+ T cell phenotype including greater CD27- CD28+ central memory, effector memory, and KLRG1- CD57+ terminally differentiated effector memory T cells (TEMRA), and fewer KLRG1+ CD57+ TEMRA cells were linked to higher biological age. Centenarians were classified into three categories: vigorous (10%), resilient (46.25%), and vulnerable (43.75%). Cytokine levels were similar across the groups. These findings challenge the notion of immunosenescence in centenarians and highlight the value of translational research in geroscience.

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Publication Details

Journal
npj Aging
Published
2026-02-16
DOI
https://doi.org/10.1038/s41514-026-00340-6
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
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article

Biological age and immunosenescence in Colombian centenarians

Juan Esteban Gallo, Jesús A. Álvarez‐Álvarez, Juan‐Manuel Anaya, Ivan David Lozada-Martinez et al.
npj Aging
Genetics, Aging, and Longevity in Model Organisms
article

Biological age and immunosenescence in Colombian centenarians

Juan Esteban Gallo, Jesús A. Álvarez‐Álvarez, Juan‐Manuel Anaya, Ivan David Lozada-Martinez, Isaura Viviana Rodríguez Torres, Manuel Rojas, Diana M. Monsalve, Olianis Pájaro, Andres Angelo Cadena Bonfanti, Brenda Guerra, Carolina Ramírez-Santana, Yeny Acosta-Ampudia, María José Díaz Gutiérrez, Edward A. Ruiz-Narváez
article en

Abstract

Biological aging and immunosenescence are central to longevity, yet their interplay in centenarians remains unclear. We conducted a cross-sectional study in 160 Colombian centenarians to examine associations between biological age (PhenoAge), immunosenescence and age-related clinical variables. Cytokine profiling (n = 114) and lymphocyte immunophenotyping (n = 42) were assessed. It was observed that better QoL and well-being were significantly associated with lower biological age, while depressive symptoms, prior tobacco use, elevated levels of RANTES and G-CSF as well as a distinct CD8+ T cell phenotype including greater CD27- CD28+ central memory, effector memory, and KLRG1- CD57+ terminally differentiated effector memory T cells (TEMRA), and fewer KLRG1+ CD57+ TEMRA cells were linked to higher biological age. Centenarians were classified into three categories: vigorous (10%), resilient (46.25%), and vulnerable (43.75%). Cytokine levels were similar across the groups. These findings challenge the notion of immunosenescence in centenarians and highlight the value of translational research in geroscience.

npj Aging
University of Michigan (US), American Society for Reproductive Medicine (US), EIA University (CO), Universidad de Antioquia (CO), University of the Coast (CO), Universidad Simón Bolívar (CO), Universidad de Medellín (CO), Universidad Autónoma de Colombia (CO), University of California, Davis (US), Universidad del Rosario (CO)
Good health and well-being
Openalex Percentile: Top 45%
Genetics, Aging, and Longevity in Model Organisms
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