1. Rhythmic profile of memory T and B-cells along childhood and adolescence.
- Author
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Brito-de-Sousa, Joaquim Pedro, Lima-Silva, Maria Luiza, Costa-Rocha, Ismael Artur da, Júnior, Luiz Roberto Alves de Oliveira, Campi-Azevedo, Ana Carolina, Peruhype-Magalhães, Vanessa, Quetz, Josiane da Silva, Coelho-dos-Reis, Jordana Grazziela Alves, Costa-Pereira, Christiane, Garcia, Cristiana Couto, Antonelli, Lis Ribeiro do Vale, Fonseca, Cristina Toscano, Lemos, Jandira Aparecida Campos, Mambrini, Juliana Vaz de Melo, Souza-Fagundes, Elaine Maria, Teixeira-Carvalho, Andréa, Faria, Ana Maria de Caetano, Gomes, Angelica Oliveira, Torres, Karen Cecília de Lima, and Martins-Filho, Olindo Assis
- Subjects
ADOLESCENCE ,B cells ,CYTOLOGY ,IMMUNOLOGIC memory ,AGE groups ,MEMORY ,PHENOTYPIC plasticity - Abstract
Immunobiography describes the life-long effects of exogenous or endogenous stimuli on remodeling of immune cell biology, including the development of memory T and B-cells. The present study aimed at investigating the rhythms of changes in phenotypic features of memory T and B-cells along childhood and adolescence. A descriptive-observational investigation was conducted including 812 healthy volunteers, clustered into six consecutive age groups (9
Mths –1Yr ; 2Yrs ; 3–4Yrs ; 5–7Yrs ; 8–10Yrs ; 11–18Yrs ). Immunophenotypic analysis of memory T-cell (CD4+ and CD8+ ) and B-cell subsets were performed by flow cytometry. The results pointed out that memory-related biomarkers of T and B-cells displayed a bimodal profile along healthy childhood and adolescence, regardless of sex. The first stage of changes occurs around 2Yrs , with predominance of naive cells, while the second and more prominent wave occurs around the age 8–10Yrs , with the prevalence of memory phenotypes. The neighborhood connectivity profile analysis demonstrated that the number of correlations reaches a peak at 11–18Yrs and lower values along the childhood. Males presented higher and conserved number of correlations when compared to females. Altogether, our results provide new insights into immunobiography and a better understanding of interactions among the cellular subsets studied here during childhood and adolescence. [ABSTRACT FROM AUTHOR]- Published
- 2023
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