Cytokine-induced Killer T Cells Enhance the Cytotoxicity Against Carboplatin-resistant Ovarian Cancer Cells

被引:3
作者
Pan, Yueh [1 ]
Chiu, Ya-Hsu [2 ]
Chiu, Shao-Chih [2 ,3 ]
Cho, Der-Yang [2 ,4 ,5 ]
Lee, Liang-Ming [1 ,6 ]
Wen, Yu-Ching [1 ,6 ]
Whang-Peng, Jacqueline [7 ,8 ]
Hsiao, Chi-Hao [1 ,6 ]
Shih, Ping-Hsiao [2 ]
机构
[1] Wan Fang Hosp, Dept Urol, Taipei, Taiwan
[2] China Med Univ Hosp, Translat Cell Therapy Ctr, Dept Med Res, 2 Yude Rd, Taichung 404332, Taiwan
[3] China Med Univ, Grad Inst Biomed Sci, Taichung, Taiwan
[4] China Med Univ, Grad Inst Immunol, Taichung, Taiwan
[5] China Med Univ Hosp, Neuropsychiat Ctr, Dept Neurosurg, Taichung, Taiwan
[6] Taipei Med Univ, Coll Med, Sch Med, Dept Urol, Taipei, Taiwan
[7] Wan Fang Hosp, Canc Ctr, Taipei, Taiwan
[8] Taipei Med Univ, Ctr Excellence Canc Res, Taipei, Taiwan
关键词
Ovarian cancer; cytokine-induced killer cell; peripheral blood mononuclear cell; chemotherapy; flow cytometry; IMMUNOTHERAPY; CHEMOTHERAPY; LYMPHOMA;
D O I
10.21873/anticanres.14376
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Ovarian cancer (OC) is typically diagnosed at an advanced stage with limitations for cure. Cytokine-induced killer (CIK) T cell therapy exerts significant cytotoxic effects against cancer cells and reduces the adverse effects of chemotherapy. Herein, we performed a flow cytometry-based method to evaluate the cytotoxicity of peripheral blood mononuclear cells-derived CIK cells against OC cells. Materials and Methods: The CIK cells were induced and expanded using an interferon-gamma/IL-2-based xeno-free medium system. The cytotoxicity of CIK cells or carboplatin against OC cells was examined. Results: The CIK cells showed an NK-like phenotypic characteristic and dose-dependently increased cytotoxicity against OC cells. We found that the number of advanced OC cells, which were more resistant to carboplatin, was dramatically decreased by an additional one-shot CIK treatment. Conclusion: CIK cells have a potent cytotoxic ability that would be explored as an alternative strategy for cancer treatment in the near future.
引用
收藏
页码:3865 / 3872
页数:8
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