Decoupled dynamics of absolute and relative lymphocyte counts and age-polarized CD4(+)/CD8(+) ratio in infants versus older adults.

BACKGROUND: Significant phenotypic and functional differences in peripheral lymphocyte subsets between infants and the elderly contribute to age-related variations in disease susceptibility and clinical outcomes. However, we are unable to specifically analyze the underlying causes owing to a lack of data on lymphocyte absolute counts and functional markers from two extremes of age. METHODS: A total of 111 infants (≤ 6 months) and 111 older adults (≥ 65 years) were enrolled to assess the percentages and absolute counts of peripheral blood lymphocyte (PBL) subsets. These included CD3(+) T cells, CD4(+) T cells, CD8(+) T cells, B cells, NK cells, naïve T cells (Tn), stem cell memory T cells (Tscm), central memory T cells (Tcm), effector memory T cells (Tem), and terminally differentiated effector memory T cells (Temra). Differences in PBL phenotypes by age group and gender were analyzed using the Wilcoxon rank-sum test. In addition, linear regression analysis was performed to examine the associations between the CD4(+)/CD8(+) ratio and various PBL subsets. RESULTS: Comparative analysis demonstrated that infants had significantly higher absolute counts of CD3(+) T cells, CD4(+) T cells, CD8(+) T cells, B cells, and both CD4(+) and CD8(+) subsets of Tn, Tscm, Tcm, and Temra (p < 0.001), despite significantly lower percentages of these cell types (p < 0.001). In contrast, older adults exhibited reduced absolute counts but relevated percentages for all the aforementioned lymphocyte subsets, except for CD4(+) and CD8(+) Tn cells, which showed lower percentages (p < 0.001). Notably, NK cells were significantly increased in both percentage and absolute count among older adults (p < 0.001). The CD4(+)/CD8(+) ratio showed marked age-related polarization, with significantly higher values in infants compared to older adults (median, 2.60 [IQR, 2.02-3.36] vs. 1.60 [IQR, 1.15-2.14]), a difference particularly pronounced in female infants (p < 0.001). Gender-related differences were observed only in the infant group, where female infants exhibited significantly higher absolute counts of CD3(+) T cells, CD3(+)CD4(+) T cells, and CD4(+) Tscm and Tcm subsets (p < 0.05). Furthermore, linear regression analysis revealed that in infants, the CD4(+)/CD8(+) ratio was positively associated with the percentages and absolute counts of CD4(+) Tn cells and the percentage of CD4(+) Tcm cells (p < 0.05), while showing a negative correlation with the percentages of CD8(+) Tn and memory T (Tm) cell subsets (p < 0.05). CONCLUSION: PBL profiles exhibit marked heterogeneity at the extremes of age, with infants showing abundant naïve and memory T cell reserves, while older adults are characterized by increased NK cell activity. The age-dependent polarization of the CD4(+)/CD8(+) ratio may serve as a potential biomarker of immunosenescence, offering valuable reference points for age-tailored vaccination strategies and immune risk stratification in the elderly.