It is well known that aging is associated with various alterations in
lymphoid cell functions, particularly with a progressive decline in im
mune responsiveness to exogenous antigens and increasing incidence of
autoimmune phenomena. Many studies have been focused on the mechanisms
of the immunologic features of aging. This review describes our resul
ts of studies performed to determine the influence of age on the capac
ity to produce interleukin-2 (IL-2), interferon-gamma (IFN-gamma), int
erleukin-4 (IL-4), interleukin-5 (IL-5), interleukin-6 (IL-6) and tumo
r necrosis factor (TNF). Mitogen-stimulated cultures of mononuclear ce
lls (MNC) from human beings were assessed for cytokine-producing capac
ity. A significant decrease in IFN-gamma and IL-2 production by MNC cu
ltures from elderly individuals was observed. No significant differenc
e was instead observed between cultures from elderly individuals and t
hose from young ones as regards TNF-alpha, IL-4 and IL-6 production. M
itogen or antigen-stimulated cultures of MNC from aged mice also displ
ayed a significant decrease in IFN-gamma and IL-2 production as well a
s TNF-beta. Instead IL-4 and IL-5 production significantly increased i
n these cultures. We suggest that this imbalanced cytokine production
may well account for the pattern of immune response which may be obser
ved in the elderly, i.e. a normal or increased humoral response (inclu
ding autoimmune responses) in face of a low T cell immune responsivene
ss.