K562细胞
白细胞介素21
白细胞介素15
免疫疗法
细胞生物学
癌症免疫疗法
白细胞介素12
Janus激酶3
过继性细胞移植
生物
免疫学
细胞因子
癌症研究
免疫系统
T细胞
细胞毒性T细胞
体外
白细胞介素
白血病
生物化学
作者
Srinivas S. Somanchi,Dean A. Lee
标识
DOI:10.1007/978-1-4939-3684-7_15
摘要
Natural killer (NK) cells have gained significant attention for adoptive immunotherapy of cancer due to their well-documented antitumor function. In order to evaluate the therapeutic efficacy of NK cell adoptive immunotherapy in preclinical models with a potential for clinical translation, there is a need for a reliable platform for ex vivo expansion of NK cells. Numerous methods are reported in literature using cytokines and feeder cells to activate and expand human NK cells, and many of these methods are limited by low-fold expansion, cytokine dependency of expanded NK cells or expansion-related senescence. In this chapter, a robust NK cell expansion protocol is described using K562 cell line gene modified to express membrane bound IL21 (K562 mb.IL21). We had previously demonstrated that this platform enables the highest fold expansion of NK cells reported in the literature to date (>47,000-folds in 21 days), and produces highly activated and pure NK cells without signs of senescence, as determined by telomere shortening.
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