Moreno María, Molling Johan W, von Mensdorff-Pouilly Silvia, Verheijen René H M, von Blomberg B Mary E, van den Eertwegh Alfons J M, Scheper Rik J, Bontkes Hetty J
Department of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Clin Immunol. 2008 Oct;129(1):145-54. doi: 10.1016/j.clim.2008.07.004. Epub 2008 Aug 15.
Invariant natural killer T (iNKT) cells play a pivotal role in cancer immunity through trans-activation of effector cells via swift cytokine secretion. In mice, iNKT cell activation by alpha-galactosylceramide (alpha-GC) induces potent NK cell-mediated anti-tumour effects. Here we investigated whether human iNKT cells could enhance NK cell functional activity in vitro. iNKT cell activation by alpha-GC treatment of peripheral blood mononuclear cells (PBMC) was not sufficient to enhance NK cell effector functions. However, addition of in vitro expanded iNKT cells to PBMC enhanced NK cell-mediated cytotoxicity in an alpha-GC-dependent manner. NK cell activation by iNKT cells was primarily mediated by soluble factors, and could be enhanced by the NK cell activating cytokine IL-21. These results suggest that adoptive transfer of ex vivo expanded iNKT cells will enhance NK cell function and is expected to enhance the efficacy of cancer immunotherapy, particularly in combination with IL-21 and alpha-GC.
不变自然杀伤T(iNKT)细胞通过迅速分泌细胞因子激活效应细胞,在癌症免疫中发挥关键作用。在小鼠中,α-半乳糖神经酰胺(α-GC)激活iNKT细胞可诱导强大的自然杀伤(NK)细胞介导的抗肿瘤效应。在此,我们研究了人iNKT细胞是否能在体外增强NK细胞的功能活性。用α-GC处理外周血单核细胞(PBMC)激活iNKT细胞不足以增强NK细胞的效应功能。然而,将体外扩增的iNKT细胞添加到PBMC中,以α-GC依赖的方式增强了NK细胞介导的细胞毒性。iNKT细胞对NK细胞的激活主要由可溶性因子介导,并且可被NK细胞激活细胞因子IL-21增强。这些结果表明,过继转移体外扩增的iNKT细胞将增强NK细胞功能,并有望提高癌症免疫治疗的疗效,特别是与IL-21和α-GC联合使用时。