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胃癌干细胞抗原负载的DC -CIK对胃癌细胞的杀伤活性[J]. 肿瘤防治研究, 2013, 40(10): 917-920. DOI: 10.3971/j.issn.1000-8578.2013.10.001
引用本文: 胃癌干细胞抗原负载的DC -CIK对胃癌细胞的杀伤活性[J]. 肿瘤防治研究, 2013, 40(10): 917-920. DOI: 10.3971/j.issn.1000-8578.2013.10.001
Killing Effect of DC-CIK Loaded with Gastric Cancer Stem Cell Antigen Against Activity of Gastric Cancer[J]. Cancer Research on Prevention and Treatment, 2013, 40(10): 917-920. DOI: 10.3971/j.issn.1000-8578.2013.10.001
Citation: Killing Effect of DC-CIK Loaded with Gastric Cancer Stem Cell Antigen Against Activity of Gastric Cancer[J]. Cancer Research on Prevention and Treatment, 2013, 40(10): 917-920. DOI: 10.3971/j.issn.1000-8578.2013.10.001

胃癌干细胞抗原负载的DC -CIK对胃癌细胞的杀伤活性

Killing Effect of DC-CIK Loaded with Gastric Cancer Stem Cell Antigen Against Activity of Gastric Cancer

  • 摘要: 目的 探讨胃癌干细胞抗原负载树突细胞(DC)联合细胞因子诱导杀伤细胞(CIK)对胃癌细 胞的影响。方法 分离人胃癌干细胞,冻融法制备抗原,将胃癌干细胞负载DC-CIK细胞,用流式细胞仪检测胃癌干细胞和DC、CIK细胞表型;将胃癌细胞与DC组、DC-CIK组、胃癌细胞抗原组、负载胃癌干细胞抗原组联合培养,用四甲基偶氮唑盐(MTT)法检测不同组别对胃癌细胞的杀伤作用。结果 经胃癌干细胞抗原刺激的DC细胞,DC表面成熟标志CD83和CD86 表达明显增加,CD83和CD86表达率为80.4%,高于DC组、DC-CIK组和胃癌细胞抗原组,差异有统计学意义(P<0.01);MTT检测结果显示:负载胃癌干细胞抗原组、胃癌细胞抗原组、DC-CIK组、DC组对胃癌细胞杀伤率分别为(80.6±0.8)%、(72.3.±0.6)%、(58.4±0.2)%和(49.7±0.8)%,组间比较差异有统计学意义(P<0.01)。结论 胃癌干细胞作为抗原刺激DC细胞,可增强树突状细胞免疫表达,促进细胞增埴,提高对胃癌细胞的杀伤作用。

     

    Abstract: Objective To investigate the killing effect of dendritic cells (DC) and cytokine-induced killer (CIK) cells loaded with gastric cancer stem cell antigens on gastric cancer cells. Methods Human gastric cancer stem cells were isolated and identifi ed. Antigens were made with the freeze-thaw method. The phenotype of DC-CIK cells loaded on gastric cancer stem cells was examined with fl ow cytometry.Gastric cancer cells were cultured in DC group,DC-CIK group,gastric cancer cell antigen group and gastric cancer stem cell antigen group respectively. Methyl thiazolyl tetrazolium (MTT )method was used to examine the killing effect of DCCIK on gastric cancer cells in each group. Results The expression of surface maturity markers CD83 and CD86 of DC cells stimulated by gastric cancer stem cell antigen signifi cantly increased to 80.4%, higher than the DC group, DC-CIK group and gastric cancer cell antigen group(P <0.01). MTT test results showed that the destruction rates of gastric cancer of gastric cancer stem cell antigen group, gastric cancer cell antigen group, DC-CIK group and DC group were (80.6 ± 0.8)%, (72.3 ± 0.6)%, (58.4 ± 0.2)% and (49.7 ± 0.8)% (P <0.01). Conclusion Stimulating DC cells as an antigen, gastric cancer stem cells could enhance the immunoreaction of dendritic cells, promote cell proliferation, and therefore improve killing effect on gastric cancer cells.

     

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