Aging is associated with an increased occurrence of infection and canc
er, and, as people age, they begin to exhibit age-related immune defic
iencies, collectively termed immunosenescence. To determine the effect
s of age on human monocytes, 'aged monocytes' (isolated from individua
ls greater than or equal to 65 years of age) were compared with 'young
monocytes' (isolated from individuals similar to 25 years of age) for
their ability to be activated by lipopolysaccharide. Our results show
that aged monocytes display a decrease in their cytotoxicity against
tumor cells in vitro, a decrease in interleukin (IL1) secretion (altho
ugh no decrease in IL1 precursor production was observed), a decrease
in reactive oxygen and nitrogen intermediate (ROI/RNI) release, an inc
rease in intracellular levels of cyclic adenosine monophosphate and a
loss of protein kinase translocation. Therefore, aged monocytes presen
t distinct characteristics of immunosenescence.