Natural killer-like nonspecific tumor cell lysis mediated by specific ligand-activated Vα14 NKT cells

Tetsu Kawano(Chiba University), Junqing Cui(Chiba University), Yasuhiko Koezuka(Chiba University), Isao Toura(Chiba University), Yoshikatsu Kaneko(Chiba University), Hiroshi Sato(Chiba University), Eisuke Kondo(Chiba University), Michishige Harada(Chiba University), Haruhiko Koseki(Chiba University), Toshinori Nakayama(Chiba University), Yujiro Tanaka(Chiba University), Masaru Taniguchi(Chiba University)
Proceedings of the National Academy of Sciences
May 12, 1998
Cited by 476Open Access

Abstract

We have recently identified alpha-galactosylceramide (alpha-GalCer) as a specific ligand for an invariant Valpha14/Vbeta8.2 T cell receptor exclusively expressed on the majority of Valpha14 NKT cells, a novel subset of lymphocytes. Here, we report that alpha-GalCer selectively activates Valpha14 NKT cells resulting in prevention of tumor metastasis. The effector mechanisms of the ligand-activated Valpha14 NKT cells seem to be mediated by natural killer (NK)-like nonspecific cytotoxicity. Indeed, the cytotoxic index obtained by alpha-GalCer-activated Valpha14 NKT cells was reduced by the addition of cold target tumor cells or by treatment with concanamycin A, which inhibits activation and secretion of perforin, but not by mAbs against molecules involved in the NKT cell recognition and conventional cytotoxicity, such as CD1d, Vbeta8, NK1. 1, Ly49C, Fas, or Fas ligand. These results suggest that the ligand-activated Valpha14 NKT cells kill tumor cells directly through a CD1d/Valpha14 T cell receptor-independent, NK-like mechanism.


Related Papers

No related papers found

Powered by citation graph analysis