Abstract:Objective To investigate aging-associated changes in serum thyroid hormone levels and cellular immune function. Methods Three groups of healthy subjects were recruited based on SENIEUR protocol criteria: group A, aged over 80 years (n = 78); group B, aged 60-79 years (n = 128); and group C, aged 20-59 years (n = 60). Serum thyroid hormone level was determined by chemiluminescence method. Peripheral blood T cells, B cells, and NK cells numbers were evaluated by flow cytometry and T cell subsets CD4+/CD8+ ratios were also calculated. In addition, 10 subjects were randomly selected from each group and their T cells were isolated from peripheral blood mononuclear cells (PBMC); T cell proliferation after phytohemagglutinin (PHA) stimulation was determined by MTT assays. Results There was no significant difference in T3 thyroid hormone (T3), T4 thyroid hormone (T4), free T3 (FT3), free T4 (FT4) and thyroid stimulating hormone (TSH) among the three groups (P>0.05). There was no marked difference in PBMC surface HLA-DR expression, as well as the absolute numbers of peripheral blood T cells, NK cells, or B cells among the three groups (P>0.05). Moreover, no significant difference was observed in the numbers of CD4+ cells, CD8+ cells, or the CD4+/CD8+ ratios (P>0.05). However, T cell proliferation was markedly increased after PHA stimulation, with the highest level in group C and the lowest level in group A (P<0.05). Conclusion The study recruits subjects based on the SENIEUR protocol criteria, and our findings suggest that the levels of serum thyroid hormone and the numbers of immune cells remain unchanged with increasing age. However, there is a trend for decreased cellular immune function with increasing age.