Motohashi Shinichiro
Dept. of Immunology, Graduate School of Medicine, Chiba University.
Gan To Kagaku Ryoho. 2007 Apr;34(4):550-3.
Human V alpha 24 natural killer T (NKT) cells bearing an invariant V alpha 24 J alpha Q antigen receptor, the counterpart of murine V alpha 14 NKT cells, are activated by a specific ligand, alpha-galactosylceramide (alpha GalCer; KRN 7000), in a CD 1 d-dependent manner. Previous findings showed that alpha GalCer-pulsed dendritic cells (DCs) exerted a strong antitumor activity in the mouse tumor metastatic models, and intravenous administration of alpha GalCer-pulsed DCs led to V alpha 14 NKT cell expansion in the lung. With these results, we performed a phase I dose escalation study of alpha GalCer-pulsed DCs treatment in patients with lung cancer. Patients with advanced non-small cell lung cancer or recurrent lung cancer received intravenous injection of alpha GalCer pulsed dendritic cell immune therapy to test the safety, feasibility, and clinical response. Immunomonitoring was also performed in all completed cases. Eleven patients were enrolled in this study, None of whom experienced severe adverse events. Peripheral blood V alpha 24 NKT cells dramatically increased after the first and second injection of alpha GalCer pulsed DCs in one patient of level 3. The clinical trial of alpha GalCer-pulsed DCs administration is well tolerated,and this therapy has been carried out safely. To obtain more conclusive findings about immune responses and antitumor responses, a phase I-II study with greater numbers of patients is ongoing.
携带恒定Vα24 JαQ抗原受体的人类Vα24自然杀伤T(NKT)细胞是小鼠Vα14 NKT细胞的对应物,可被特异性配体α-半乳糖神经酰胺(αGalCer;KRN 7000)以CD1d依赖的方式激活。先前的研究结果表明,αGalCer脉冲树突状细胞(DC)在小鼠肿瘤转移模型中具有强大的抗肿瘤活性,静脉注射αGalCer脉冲DC可导致肺中Vα14 NKT细胞扩增。基于这些结果,我们对肺癌患者进行了αGalCer脉冲DC治疗的I期剂量递增研究。晚期非小细胞肺癌或复发性肺癌患者接受静脉注射αGalCer脉冲树突状细胞免疫治疗,以测试其安全性、可行性和临床反应。还对所有完成的病例进行了免疫监测。本研究共纳入11例患者,均未发生严重不良事件。在1例3级患者中,首次和第二次注射αGalCer脉冲DC后,外周血Vα24 NKT细胞显著增加。αGalCer脉冲DC给药的临床试验耐受性良好,且该治疗已安全实施。为了获得更多关于免疫反应和抗肿瘤反应的确切结果,一项纳入更多患者的I-II期研究正在进行中。