文章摘要
Zhihua Wang,li Qin,Chunyan Zhang,Yuyan Ma. Effect of IL-12 on the proliferation and cytotoxicity of CIK cells to gastric adenocarcinoma cell BGC-823. Oncol Transl Med, 2014, 13: 355-359.
IL-12对胃腺癌细胞BGC-823诱导的杀伤细胞的增值和细胞毒性作用
Effect of IL-12 on the proliferation and cytotoxicity of CIK cells to gastric adenocarcinoma cell BGC-823
Received:July 01, 2014  Revised:July 28, 2014
DOI:10.1007/s10330-014-0021-4
中文关键词: 细胞因子诱导的杀伤细胞;白介素-12;增殖能力;细胞毒性
英文关键词: Cytokine-induced killer (CIK) cell; interleukin-12 (IL-12); proliferative ability; cytotoxicity
基金项目:本课题受国家“九五”重点攻关课题(96-960A-01-20)和黑龙江省重点攻关课题(G00C190401)基金资助
Author NameAffiliationE-mail
Zhihua Wang* Hefei Fenghuang Tumor Hospital, Hefei 267800, China
Cancer Research Institute of Harbin Medical University, Harbin 150081, China 
hljwzh000@163.com 
li Qin Cancer Research Institute of Harbin Medical University, Harbin 150081, China  
Chunyan Zhang Cancer Research Institute of Harbin Medical University, Harbin 150081, China  
Yuyan Ma Cancer Research Institute of Harbin Medical University, Harbin 150081, China  
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中文摘要:
  目的:观察IL-12对细胞因子诱导的杀伤细胞(cytokine-induced killer cells, CIK)体外扩增的影响。方法:采用三种不同的细胞因子组合扩增CIK细胞,即IL-2组:IFN-γ、CD3单抗、IL-1和IL-2; IL-2加IL-12组:IFN-γ、CD3单抗、IL-1、IL-2和IL-12;IL-12组:IFN-γ、CD3单抗、IL-1和IL-12。细胞计数法测定细胞的增殖、流式细胞术分析细胞表型,MTT法测定细胞毒作用。 结果:三种方法均可使细胞增殖能力显著增加,对CD3 CD56 细胞的诱导作用也无明显差异,IL-12与IL-2联合作用组促增殖能力和细胞毒性作用明显强于其他两组(P<0.05)。结论:IL-12同样可以用于CIK细胞的诱导,而联合IL-12与IL-2可以显著增强CIK细胞的增殖能力和细胞毒性。
英文摘要:
    Objective: The aim of the study was to evaluate the effect of interleukin-12 (IL-12) on the proliferation and cytotoxicity of cytokine-induced killer (CIK) cells in vitro. Methods: Three different combinations of cytokines, IL-2, IL-12 IL-2, and IL-12, were used to proliferate CIK cells, adding IFN-γ, IL-1 and CD3 McAb in each one. Phenotype of the cells was analyzed by flow cytometry. The cellular proliferation and cytotoxic activity were determined by cytometry and MTT assay. Results: CIK cells generated by the three methods showed high reproductive activity, and no obviously difference in inducing CD3 CD56 cells was found among the three groups. The group of IL-2 IL-12 evidently enhanced both the proliferation and the cytotoxicity of the CIK cells compared with the other two groups (P < 0.05). Conclusion: IL-12 could be used to induce the CIK cells as well as IL-2. CIK cells induced by combining IL-12 with IL-2 had stronger proliferative ability and higher cytotoxicity to tumor cells in vitro, which could be used as a potential anti-tumor adoptive immunotherapy in clinic.
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