Age-associated thymic involution manifests its effects in a variety of
ways that are related to a loss of T cell function. These include the
appearance of a non-functional subset of T cells that increase in rep
resentation with age. Moreover there is a loss of T cell proliferative
ability, a decline in the synthesis and release of interleukin-2 (IL-
2), a decline in the ability of the T cell to express the IL-2 recepto
r, and a loss of control activity. This loss of control is demonstrate
d by the age-related appearance of autoantibodies and an increase in t
he elaboration of inflammatory cytokines such as TNF, IFN, IL-6, and T
GF. A major part of the basis for the loss of T cell function is an in
ability of the T cell to respond to activation signals that are transm
itted through the membrane binding of specific stimulatory signals. Tr
ansduction events, differentiation signals, and a loss of control mech
anisms are all parts of a complicated picture of age-related immune de
ficiencies.