Preclinical evaluation of DC-CIK cells as potentially effective immunotherapy model for the treatment of glioblastoma

细胞因子诱导的杀伤细胞 免疫疗法 细胞毒性T细胞 癌症研究 医学 细胞因子 免疫学 胶质瘤 生物 免疫系统 CD8型 体外 CD3型 生物化学
作者
Amanda Luck,Jingjing Pu,Ahmad Melhem,Matthias Schneider,Amit Sharma,Ingo G.H. Schmidt‐Wolf,Jarek Maciaczyk
出处
期刊:Scientific Reports [Springer Nature]
卷期号:15 (1)
标识
DOI:10.1038/s41598-024-84284-5
摘要

Abstract Despite the favorable effects of immunotherapies in multiple types of cancers, its complete success in CNS malignancies remains challenging. Recently, a successful clinical trial of cytokine-induced killer (CIK) cell immunotherapy in patients with glioblastoma (GBM) has opened a new avenue for adoptive cellular immunotherapies in CNS malignancies. Prompt from these findings, herein, we investigated whether dendritic cells (DC) in combination with cytokine-induced killer cells (DC-CIK) could also provide an alternative and more effective way to improve the efficacy of GBM treatment. The analysis showed that DC-CIK cells exerted a significant cytotoxic effect on the glioblastoma cell lines, especially with the phenotype of stem-like cells (GSCs). In addition, the increased specific lysis of these cells subsequent to DC-CIK co-culture was confirmed with confocal fluorescence microscope. The direct interactions between tumor and effector cells were found to be highly effective in GBM organoids (GBOs). Moreover, a significant increase in apoptosis and elevated levels of IFN-γ (and not TNF-α) secretion were observed as a targeting mechanism of DC-CIK cells against GBM cell models. Overall, we provide important preliminary evidence that DC-CIK cells may have potential in the treatment of CNS malignancies, particularly glioblastoma.

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