Lin Jhih-Ni, Kuan Che-Yung, Chang Chia-Ting, Chen Zhi-Yu, Kuo Wei-Ting, Lin Jason, Lin Yu-Ying, Yang I-Hsuan, Lin Feng-Huei
Institute of Biomedical Engineering and Nanomedicine, National Health Research Institutes, No. 35, Keyan Road, Zhunan, Miaoli, 35053, Taiwan.
Department of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No. 49, Fanglan Rd, Taipei, 10672, Taiwan.
J Biol Eng. 2024 Nov 12;18(1):65. doi: 10.1186/s13036-024-00461-0.
The NK-92MI cell line has displayed significant promise in clinical trials for cancer treatment. However, challenges persist in obtaining sufficient cell quantities and achieving optimal cytotoxicity. The proliferation of natural killer (NK) cells involves the formation of cell aggregates, but excessively large aggregates can impede nutrient and waste transport, leading to reduced cell survival rates. In this study, a custom bioreactor was designed to mimic pseudostatic culture conditions by integrating brief mechanical rotation during a 6-h static culture period. This method aimed to achieve an optimal aggregate size while improving cell viability. The findings revealed a 144-fold expansion of 3D NK-92MI cell aggregates, reaching an ideal size of 80-150 µm, significantly increasing both cell proliferation and survival rates. After 14 days of culture, the NK-92MI cells maintained their phenotype during the subsequent phase of cell activation. Moreover, these cells presented elevated levels of IFN-γ expression after IL-18 activation, resulting in enhanced NK cell-mediated cytotoxicity against K562 cells. This innovative strategy, which uses a closed suspension-based culture system, presents a promising approach for improving cell expansion and activation techniques in immunocellular therapy.
NK-92MI细胞系在癌症治疗的临床试验中已显示出显著的前景。然而,在获得足够的细胞数量和实现最佳细胞毒性方面仍存在挑战。自然杀伤(NK)细胞的增殖涉及细胞聚集体的形成,但过大的聚集体会阻碍营养物质和废物的运输,导致细胞存活率降低。在本研究中,设计了一种定制生物反应器,通过在6小时静态培养期内整合短暂的机械旋转来模拟伪静态培养条件。该方法旨在实现最佳聚集体大小,同时提高细胞活力。研究结果显示,3D NK-92MI细胞聚集体扩大了144倍,达到80-150 µm的理想大小,显著提高了细胞增殖率和存活率。培养14天后,NK-92MI细胞在随后的细胞激活阶段保持其表型。此外,这些细胞在IL-18激活后IFN-γ表达水平升高,导致NK细胞介导的对K562细胞的细胞毒性增强。这种使用基于封闭悬浮培养系统的创新策略,为改进免疫细胞治疗中的细胞扩增和激活技术提供了一种有前景的方法。