Interleukin 2 and interleukin 15 differentially predispose natural killer cells to apoptosis mediated by endothelial and tumour cells

Human natural killer (NK) cells constitutively express the beta- and gamma -chains of the interleukin 2 (IL-2)/IL-15 receptor, and both IL-2 and IL-15 are able to activate NK cell proliferation and cytotoxicity. When IL-2-pri med human NK cells are exposed to sensitive targets (i.e. K562) they underg o apoptosis mediated by the beta (2)-integrin CD18. Here, we demonstrate th at: (i) endothelial cells, similar to K562 tumour target cells, induce apop tosis of IL-2-primed NK cells; (ii) endothelial- and K562 cell-induced apop tosis is significantly lower in IL-15 than in IL-2-stimulated NK cells: (ii i) a critical role in the apoptosis of IL-2-primed NK cells is played by th e alpha -chain of the IL-2 receptor. Our data show for the first time that IL-2-activated NK cells can die by apoptosis upon contact with the vascular endothelium. which is a necessary step for their extravasation. with a dir ect pathophysiological relevance on the strategy of adoptive immunotherapy of cancer. On the other hand. IL-15, although generating a similar level of activation of NK cells, largely prevents their apoptotic fate. Therefore, IL-15 produced early in the immune response, when T cells are not yet activ ated, generates lymphokine-activated killer cells that are efficient killer s relatively protected from apoptosis. Once activated, T cells produce IL-2 that overcomes the effect of IL-15 on NK cells. paving the way for their d eath by apoptosis.