Immunosenescence is a process that primarily affects the T cell compartment
of the immune system, although age-associated immunological alterations ha
ve: also been demonstrated in the NK cell phenotype and function. A signifi
cant expansion in the number of NK cells is found in aging. The NK cytotoxi
c capacity of total peripheral blood lymphocytes is also well preserved, no
t only in healthy elderly people but also in centenarians. However, NK cell
killing of K562 is impaired when considered in a per-cell basis, and this
defect is associated with defective signal transduction after activation mo
re than a diminished conjugate formation or killing capacity. We have studi
ed the phenotype of NK cells in elderly donors fulfilling the Senieur crite
ria. We have also studied the capacity of these cells to be activated by IL
2 when different NR cell functions, other than cytotoxicity, are considered
. Our results confirm the increased percentage of NK cells in the elderly d
ue to the expansion of the CD56(dim) subset that also show an altered patte
rn of activation markers, whereas no differences were found in the CD56(bri
tght) subset. The response of NK cells to IL2 was found to be impaired when
proliferation, expression of CD69, and Ca2+ mobilization were considered,
whereas TNF-alpha production was not significantly affected, These results
suggest that human NK cells do not escape the aging process, although senes
cence have a differential effect on distinct NK cell biological functions,
ranging from severe to negligible impairment, depending on the parameters c
onsidered. (C) 1999 Elsevier Science Inc. All rights reserved.