细胞因子诱导的杀伤细胞
K562细胞
外周血单个核细胞
白细胞介素12
细胞毒性
细胞因子
髓系白血病
化学
免疫学
白细胞介素21
白细胞介素15
CD3型
细胞毒性T细胞
白血病
癌症研究
体外
白细胞介素
生物
免疫系统
CD8型
生物化学
作者
Qianshan Tao,Tianping Chen,Lili Tao,Huiping Wang,Ying Pan,Shudao Xiong,Zhimin Zhai
出处
期刊:Journal of Immunotherapy
[Ovid Technologies (Wolters Kluwer)]
日期:2013-10-21
卷期号:36 (9): 462-467
被引量:42
标识
DOI:10.1097/cji.0000000000000001
摘要
Cytokine-induced killer (CIK) cells are usually generated from peripheral blood mononuclear cells with the stimulation of IL-2 in vitro. Unlike the conventional IL-2-stimulated CIK cells (IL-2-CIK cells), we investigated the characteristics and potential mechanism of IL-15-stimulated CIK cells (IL-15-CIK cells) in this study. Compared with IL-2-CIK cells, the percentage of CD3CD56 cells was significantly increased in IL-15-CIK cells, but the expression of regulatory T (Treg) cells and IL-35 was significantly decreased in IL-15-CIK cells. Meanwhile, the in vitro cytotoxicity against human myeloid leukemia cells K562 of IL-15-CIK cells was significantly augmented compared with IL-2-CIK cells. These data suggest that IL-15 may improve the cytotoxicity of CIK cells against leukemia cells by upregulating CD3CD56 cells and downregulating Treg cells and IL-35.
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