Immunosenescence is a process that affects all cell compartments of the imm
une system. Age-associated changes have been demonstrated not only on T lym
phocytes but also in different aspects of the innate immunity including nat
ural killer (NK) cells. A significant expansion in the percentage of NK cel
ls showing a mature phenotype has been found in healthy elderly donors, and
the NK-cytotoxic capacity of total peripheral blood lymphocytes is well pr
eserved in these individuals. However, NK-cell killing of K562 is impaired
when considered on a per-cell basis. Furthermore, NK cells from elderly peo
ple show a decreased proliferative response to interleukin 2 and a parallel
impaired expression of the CD69 activation antigen. The response to interl
eukin 2 of NK cells from aged donors is also impaired in terms of their cap
acity to kill NK-resistant cell lines, but not when K562 killing, perforin
synthesis, or tumor necrosis factor alpha production are considered. Theref
ore phenotypic and functional alterations can be shown in NK cells in healt
hy aging. These changes are compatible with the expansion of a mature NK su
bset. (C) 1999 Elsevier Science Inc. All rights reserved.