医学
自然杀伤性T细胞
免疫疗法
肺癌
免疫系统
阿尔法(金融)
免疫学
肺
癌症研究
T细胞
内科学
外科
结构效度
患者满意度
出处
期刊:PubMed
[National Institutes of Health]
日期:2007-04-01
卷期号:34 (4): 550-3
被引量:5
摘要
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.
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