e. interaction with MHC class Ilow cells, might be a priming signal for NK cells whereas NKG2D engagement is a triggering signal. To test this hypothesis we did coincubation, transplantation and chromium release experiments comparing several lymphoma cell lines that differed with regard to MHC class I and NKG2D-L expression (Table 1). MHC class Ilow but not MHC class Ihigh cells caused NK-cell activation in inoculated WT mice and in coincubation experiments (Table 1). However, NK-cell activation by MHC class Ilow cells was not sufficient for mediating cytotoxicity and tumor elimination. Both, cytotoxicity in vitro

and rejection in vivo additionally required NKG2D-L expression by the target cells. Thus, all tumor cell BGB324 order lines showed the same requirements for NK-cell function as the myc-B and myc-E cell lines (Fig. 4A, Table 1). The dependence

of in vitro cytotoxicity on “missing self” could be overcome PD0325901 ic50 by pre-activating NK cells with IL-15 in vitro or with DC injected into the NK-cell donors. Notably, this treatment could not restore cytotoxicity if target cells did not express NKG2D-L (Table 1). Since effector functions of NK cells from clinically-unapparent λ-myc mice were reduced but could be restored by in vitro activation with CpG-ODN (Fig. 2C) that are strong NK-cell stimulators 31, 32, we examined whether NK cell-activating agents may delay tumor development in vivo through an NK cell-mediated mechanism. We therefore treated clinically unapparent λ-myc mice with CpG-ODN 1668 for several weeks. Treated animals exhibited a statistically significant survival benefit (p<0.005; Fig. 5). To uncover the role of NK cells in this system, we depleted λ-myc mice of NK cells by using Ab during CpG-ODN treatment. No statistically significant delay of tumor development was observed in these animals as

compared with λ-myc mice that did not receive CpG-ODN. Since NK-cell depletion was sufficient for reversing the CpG-ODN-induced effect, the CpG-mediated survival RVX-208 benefit is dependent on NK-cell activation although an additional effect of T cells cannot be completely precluded. In summary, NK-cell activation can delay endogenous lymphoma growth when applied during early steps of tumorigenesis. The observation that MHC class I recovery and loss of NKG2D-L may contribute to tumor escape suggests that NK cells play a role in immune surveillance of lymphomas. However, despite showing an activated phenotype, NK cells from tumor-bearing λ-myc transgenic mice failed to exert effector functions such as cytotoxicity against NK-sensitive targets and IFN-γ expression. Impaired NK-cell functions have also been described in cancer patients 33, 34. For example, lower levels of NCR and reduced lytic activity were reported for NK cells of patients with acute myeloid leukemia 33. Controversial results were obtained in tumor transplantation models of the mouse.