Haraguchi Kyoko, Takahashi Tsuyoshi, Nakahara Fumio, Matsumoto Akihiko, Kurokawa Mineo, Ogawa Seishi, Oda Hideaki, Hirai Hisamaru, Chiba Shigeru
Department of Hematology/Oncology, University of Tokyo Graduate School of Medicine and Hospital, Hongo, Tokyo, Japan.
Leuk Lymphoma. 2006 Oct;47(10):2218-23. doi: 10.1080/10428190600682688.
Invariant natural killer T (iNKT) cells are thought to regulate anti-tumor immunity. Human iNKT (i.e. Valpha24+ NKT) cells have been reported to recognize CD1d on target cells and show cytotoxicity directly on the target cells in vitro. However, the anti-tumor effect of mouse iNKT (i.e. Valpha14+ NKT) cells has been repeatedly reported to be dependent on the activity of natural killer (NK) cells via interferon-gamma, with no evidence of direct cytotoxicity. In the present study, we report that in vitro cytolysis of EL-4 mouse lymphoblastic lymphoma cells by Valpha24+ NKT cells and in vivo eradication of these cells are both dependent on the level of CD1d expression on the tumor cell surface. These observations possibly suggest that direct cytotoxicity of tumor cells by iNKT cells is common to both humans and mice, and that the high expression level of CD1d may be a predictor whether the tumor is a good target of iNKT cells.
不变自然杀伤T(iNKT)细胞被认为可调节抗肿瘤免疫。据报道,人类iNKT(即Vα24 + NKT)细胞可识别靶细胞上的CD1d,并在体外对靶细胞直接表现出细胞毒性。然而,小鼠iNKT(即Vα14 + NKT)细胞的抗肿瘤作用已被反复报道依赖于自然杀伤(NK)细胞通过干扰素-γ发挥的活性,没有直接细胞毒性的证据。在本研究中,我们报告Vα24 + NKT细胞对EL-4小鼠淋巴细胞性淋巴瘤细胞的体外细胞溶解以及这些细胞在体内的清除均依赖于肿瘤细胞表面CD1d的表达水平。这些观察结果可能表明,iNKT细胞对肿瘤细胞的直接细胞毒性在人类和小鼠中都是常见的,并且CD1d的高表达水平可能是肿瘤是否是iNKT细胞良好靶标的预测指标。