Age-related changes in functional subsets of lymphocytes may influence the
potential to build up immune responses. In particular, the capacity of tons
illar lymphocytes to counter infections may be altered during ageing. In or
der to address this question we investigated the proportional distribution
of several subsets of tonsillar T and B cells with regard to ageing. Tonsil
s were derived from 119 patients between 2 and 65 years of age. Lymphocyte
subsets were monitored by three-colour fluorescence of relevant CD markers
in flow cytometry. As a general tendency the percentage of CD3(+) T cells s
teadily increased whereas that of CD19(+) B cells decreased at the same tim
e. No significant differences were observed between lymphocytes of patients
with and without inflammatory history of the tonsils. The percentage of CD
8(+) T cells declined whereas that of CD4(+) T cells increased during the s
ame time span. CD45RA(+) T cells increased during the first two decades of
life and gradually decreased thereafter. In contrast, CD45RO(+) T cells sho
wed an opposite trend. No differences were seen in the population of CD3(-)
/CD56(+) natural killer (NK) cells. The mature B cell marker CD40 showed no
significant changes during ageing. However, CD38(+) B cells, representing
B cells of late maturation stages, dramatically declined up to the age of 6
5. In a similar manner the CD5(+) subpopulation of B cells decreased during
ageing. Substantial changes in major tonsillar T and B cell populations as
shown in this study may have an impact on the ageing process of the immune
system.