Human invariant valpha24+ natural killer T cells activated by alpha-galactosylceramide (KRN7000) have cytotoxic antitumour activity through mechanisms distinct from T cells and natural killer cells.

Human Vα24 + NKT cells, a subpopulation of natural killer cell receptor (NKR-P1A) expressing T cells with an invariant T-cell receptor (TCR; Vα24JαQ) are stimulated by the glycolipid, α-galactosylceramide (KRN7000), in a CD1d-dependent, TCR-mediated fashion. Little is known about Vα14 + NKT-cell function. The murine counterpart, Vα14 + NKT cells, appear to have an important role in controlling malignancy. There are no human data examining the role of Vα24 + NKT cells in controlling human malignancy. We report that Vα24 + NKT cells have perforin-mediated cytotoxicity against haemopoietic malignancies. Vα24 TCR, CD1d and α-galactosylceramide may all play a role in cytotoxicity but are not absolute requirements. The greatest cytotoxicity was observed against the U937 tumour cell line (95 ± 5% lysis). THP-1, Molt4, CIR cells and allogeneic mismatched dendritic cells were also sensitive to Vα24 + NKT cytotoxicity but neither the NK target, K562, nor lymphokine-activated killer-sensitive Daudi cells, were sensitive. These results indicate a killing pattern distinct from conventional major histocompatibility complex-restricted T cells, NK cells and other cytotoxic lymphoid cells previously described. We conclude that human Vα24 + NKT cells have cytotoxic anti-tumour activity against haemopoietic malignancies through effector mechanisms distinct from conventional T cells and NK cells and that their specific stimulator KRN7000 may have therapeutic potential