Analysis of T and NK cell subsets in the Sicilian population from young to supercentenarian: The role of age and gender

Author:

Ligotti Mattia Emanuela12,Aiello Anna1,Accardi Giulia1,Aprile Stefano13,Bonura Floriana4,Bulati Matteo5,Gervasi Francesco6,Giammanco Giovanni M4,Pojero Fanny1,Zareian Nahid2,Caruso Calogero1ORCID,Farzaneh Farzin2,Candore Giuseppina1

Affiliation:

1. Laboratory of Immunopathology and Immunosenescence, Department of Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, Palermo, Italy

2. School of Cancer and Pharmaceutical Sciences, King's College London, The Rayne Institute, London, UK

3. Unit of Transfusion Medicine, San Giovanni di Dio Hospital, Agrigento, Italy

4. Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, Microbiology Section, University of Palermo, Palermo, Italy

5. Research Department, Mediterranean Institute for Transplantation and Advanced Specialized Therapies (IRCCS ISMETT), Palermo, Italy

6. Specialistic Oncology Laboratory Unit, ARNAS Hospitals Civico, Di Cristina e Benfratelli, Palermo, Italy

Abstract

Summary Ageing dramatically affects number and function of both innate and adaptive arms of immune system, particularly T cell subsets, contributing to reduced vaccination efficacy, decreased resistance to infections and increased prevalence of cancer in older people. In the present paper, we analysed the age-related changes in the absolute number of lymphocytes in 214 Sicilian subjects, and in the percentages of T and natural killer (NK) cells in a subcohort of donors. We compared these results with the immunophenotype of the oldest living Italian supercentenarian (aged 111 years). The results were also sorted by gender. The correlation between number/percentage of cells and age in all individuals. and separately in males and females, was examined using a simple linear regression analysis. We did not record the increase in the rate of inversion of the CD4/CD8 ratio, frequently reported as being associated with ageing in literature. Our observation was the direct consequence of a flat average trend of CD4+ and CD8+ T cell percentages in ageing donors, even when gender differences were included. Our results also suggest that CD4+ and CD8+ subsets are not affected equally by age comparing females with males, and we speculated that gender may affect the response to cytomegalovirus (CMV) infection. The supercentenarian showed a unique immunophenotypic signature regarding the relative percentages of her T cell subsets, with CD4+ and CD8+ T cell percentages and CD4+ naive T cell values in line with those recorded for the octogenarian subjects. This suggests that the supercentenarian has a naive ‘younger’ T cell profile comparable to that of a >80-year-old female.

Funder

Italian Ministry of Education

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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