NKG2D公司
淋巴因子激活杀伤细胞
白细胞介素12
白细胞介素21
外周血单个核细胞
NK-92
细胞毒性
Janus激酶3
免疫监视
免疫疗法
自然杀伤细胞
白细胞介素15
免疫系统
生物
免疫学
癌症研究
细胞毒性T细胞
T细胞
白细胞介素
生物化学
体外
细胞因子
作者
Min Liu,Meng Yuan,Leisheng Zhang,Zhongchao Han,Xiaoming Feng
标识
DOI:10.1016/j.bbrc.2020.12.012
摘要
Natural killer (NK) cells are pivotal effector lymphocytes characterized for the innate immune response to pathogenic microorganism and tumor cells without priming and sensitization. Despite emerging knowledge has highlighted the rosy prospects in tumor immunosurveillance, yet the large-scale clinical application of NK cell-based therapy is hindered largely attributes to the defects in generating sufficient and high-quality cellular products. Herein, on the basis of 16 kinds of candidate combinations, we investigated the feasibility of cytokine cocktail-based strategy for convenient and standardized NK cell cultivation as well as the multifaceted characteristics and cytotoxicity against tumor cells. Our results revealed that joint utilization of Interleukin (IL)-2, IL-15, IL-18 manifested the optimal facilitation upon the ex vivo expansion and proportion of NK cells in peripheral blood mononuclear cells (PBMCs). Meanwhile, the obtained NK cell population expressed high levels of activating molecules (CD16 and NKG2D) and exhibited splendid cytotoxicity against K562 cell line. Collectively, with the aid of cytokine-based programming, we established an alternative strategy for facilitating the large-scale persistence and activation of NK cells from peripheral blood, which would benefit the NK cell- and chimeric antigen receptor-modified NK (CAR-NK) cell-based autologous or allogeneic tumor immunotherapy.
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