Kawano T, Cui J, Koezuka Y, Toura I, Kaneko Y, Sato H, Kondo E, Harada M, Koseki H, Nakayama T, Tanaka Y, Taniguchi M
Core Research for Evolutional Science and Technology Project, Japan Science and Technology Corporation and Division of Molecular Immunology, Center for Biomedical Science, School of Medicine, Chiba University, 1-8-1 Inohana, Chuo, Chiba 260-8670, Japan.
Proc Natl Acad Sci U S A. 1998 May 12;95(10):5690-3. doi: 10.1073/pnas.95.10.5690.
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.
我们最近鉴定出α-半乳糖神经酰胺(α-GalCer)是一种特异性配体,它能与一种仅在大多数Vα14自然杀伤T细胞(一种新型淋巴细胞亚群)上表达的恒定Vα14/Vβ8.2 T细胞受体结合。在此,我们报告α-GalCer可选择性激活Vα14自然杀伤T细胞,从而预防肿瘤转移。配体激活的Vα14自然杀伤T细胞的效应机制似乎是由自然杀伤(NK)样非特异性细胞毒性介导的。实际上,添加冷靶肿瘤细胞或用抑制穿孔素激活和分泌的 concanamycin A处理后,α-GalCer激活的Vα14自然杀伤T细胞的细胞毒性指数降低,但针对参与自然杀伤T细胞识别和传统细胞毒性的分子(如CD1d、Vβ8、NK1.1、Ly49C、Fas或Fas配体)的单克隆抗体处理则不会使其降低。这些结果表明,配体激活的Vα14自然杀伤T细胞通过一种不依赖CD1d/Vα14 T细胞受体的NK样机制直接杀伤肿瘤细胞。