首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Generation of antitumor invariant natural killer T cell lines in multiple myeloma and promotion of their functions via lenalidomide: a strategy for immunotherapy.
【24h】

Generation of antitumor invariant natural killer T cell lines in multiple myeloma and promotion of their functions via lenalidomide: a strategy for immunotherapy.

机译:在多发性骨髓瘤中产生抗肿瘤不变的天然杀伤性T细胞系,并通过来那度胺增强其功能:一种免疫疗法。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

PURPOSE: CD1d-restricted invariant natural killer T (iNKT) cells are important immunoregulatory cells in antitumor immune responses. However, the quantitative and qualitative defects of iNKT cells in advanced multiple myeloma hamper their antitumor effects. Therefore, the development of functional iNKT cells may provide a novel strategy for the immunotherapy in multiple myeloma. EXPERIMENTAL DESIGN: We activated and expanded iNKT cells from multiple myeloma patients with alpha-galactosylceramide (alpha-GalCer)-pulsed dendritic cells, characterized their antitumor effects by the cytokine production profile and cytotoxicity against multiple myeloma cells, and explored the effects of immunomodulatory drug lenalidomide on these iNKT cells. We also investigated the expression of CD1d by primary multiple myeloma cells and its function to activate iNKT cells. RESULTS: We established highly purified functional iNKT cell lines from newly diagnosed and advanced multiple myeloma patients. These CD1d-restricted iNKT cell lines produced high level of antitumor Th1 cytokine in response to alpha-GalCer-pulsed primary multiple myeloma cells, CD1d-transfected MM1S cell line, and dendritic cells. Moreover, iNKT cell lines displayed strong cytotoxicity against alpha-GalCer-pulsed primary multiple myeloma cells. Importantly, lenalidomide further augmented the Th1 polarization by iNKT cell lines via increased Th1 cytokine production and reduced Th2 cytokine production. We also showed that CD1d was expressed in primary multiple myeloma cells at mRNA and protein levels from the majority of multiple myeloma patients, but not in normal plasma cells and multiple myeloma cell lines, and CD1d(+) primary multiple myeloma cells presented antigens to activate iNKT cell lines. CONCLUSIONS: Taken together, our results provide the preclinical evidence for the iNKT cell-mediated immunotherapy and a rationale for their use in combination with lenalidomide in multiple myeloma treatment.
机译:目的:限制CD1d不变的自然杀伤T细胞(iNKT)是抗肿瘤免疫反应中重要的免疫调节细胞。然而,晚期多发性骨髓瘤中iNKT细胞的数量和质量缺陷阻碍了其抗肿瘤作用。因此,功能性iNKT细胞的发展可能为多发性骨髓瘤的免疫治疗提供一种新的策略。实验设计:我们用α-半乳糖苷神经酰胺(α-GalCer)脉冲树突状细胞激活和扩增了多发性骨髓瘤患者的iNKT细胞,通过细胞因子的产生概况和对多发性骨髓瘤细胞的细胞毒性来表征其抗肿瘤作用,并探索了免疫调节药物的作用来那度胺对这些iNKT细胞的作用。我们还研究了原发性多发性骨髓瘤细胞CD1d的表达及其激活iNKT细胞的功能。结果:我们从新诊断和晚期多发性骨髓瘤患者中建立了高度纯化的功能性iNKT细胞系。这些CD1d限制的iNKT细胞系对α-GalCer脉冲的原发性多发性骨髓瘤细胞,CD1d转染的MM1S细胞系和树突状细胞产生了高水平的抗肿瘤Th1细胞因子。而且,iNKT细胞系对α-GalCer脉冲的原发性多发性骨髓瘤细胞显示出强大的细胞毒性。重要的是,来那度胺通过增加Th1细胞因子的产生和Th2细胞因子的产生来进一步增强iNKT细胞系的Th1极化。我们还显示,CD1d在大多数多发性骨髓瘤患者的原发性多发性骨髓瘤细胞中以mRNA和蛋白水平表达,但在正常浆细胞和多发性骨髓瘤细胞系中不表达,并且CD1d(+)原发性多发性骨髓瘤细胞呈递激活抗原。 iNKT细胞系。结论:综上所述,我们的结果为iNKT细胞介导的免疫疗法提供了临床前证据,并为他们与来那度胺联合用于多发性骨髓瘤治疗提供了理论依据。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号