Year: 2025
Type: article
Study design: Observational Study
Abstract: This study investigates how puberty affects T-cell subpopulations in healthy individuals, aiming to understand why kidney transplant outcomes are worse during adolescence. We hypothesize that pubertal maturation shifts the immune system towards a more pro-inflammatory phenotype. To explore this, we examined T-cell subtypes in individuals aged 8-30y. Pubertal maturation was assessed in 66 healthy individuals (median age: 17y, 42% male) using skeletal age and Tanner stage, and individuals were subsequently classified into one of four pubertal stages (pre-: n = 10, early-: n = 8, late-: n = 6, and post-puberty: n = 42). Multiple differentiation stages of CD4, CD8, and TCRγδ T-cells subpopulations were determined in peripheral blood samples using flow cytometry. Our results showed that absolute naïve CD4 T-cell and recent thymic emigrant CD4 T-cell counts generally decreased over the course of puberty (p = 0.004, p = 0.015), while absolute CD4 effector memory cell counts increased (p = 0.002). Notably, higher absolute naïve CD4 T-cell counts were observed during early-puberty compared to post-puberty which could not be explained by aging (p = 0.19). These findings indicate a developmental shift during puberty from a naïve to a more mature T-cell profile, supporting the idea that pubertal maturation affects the composition of the immune system.
Source: Scientific Reports
Institutions: Erasmus MC - Sophia Children’s Hospital, Erasmus MC Transplant Institute, Erasmus MC, Emma Kinderziekenhuis, Amsterdam University Medical Centers, Amsterdam institute for Immunology and Infectious Diseases, Radboud University Nijmegen, Radboud University Medical Center, Amalia Kinderziekenhuis
Language: English
Topic: T-cell and B-cell Immunology
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,690
Award: G946871821
OpenAlex ID: W4417114952
