Li Dan, Yu Hong, Xu Teng Fei, Li Jing Hua, Sun Yun Fang, Zhang Wen Qing
Department of Microbiology, Medical College of Qingdao University, Qingdao, China.
Cell Mol Immunol. 2008 Jun;5(3):225-30. doi: 10.1038/cmi.2008.28.
The aim of this project was to investigate the anti-tumor effect of an IL-12 gene modified mammary sarcoma murine cell line, EMT6/IL-12, in mouse model. In this study, we transfected the recombinant eukaryotic plasmid encoding IL-12 gene (pcDNA6-p70) into EMT6 and obtained the IL-12 expressing EMT6/IL-12 cell line. Then EMT6/IL-12 cells were s.c. inoculated into mice. The recombinant vector treatment group was set as control. We then evaluated the inhibition of tumor growth and the anti-tumor immunity function in vivo such as cytotoxicity, proliferation of splenocytes and serial IFN-gamma level. And the percentage of IFN-gamma producing CD4 or CD8 T cells among splenocytes was also analyzed in tumor bearing mice. Our results showed that the growth of tumors was obviously inhibited in EMT6/IL-12 group. Moreover, the capacities of anti-tumor immunity were all significantly higher in EMT6/IL-12 group compared to the controls. The results of the present investigation support the notion that EMT6/IL-12 could exert gene therapy in tumor model by improving the anti-tumor cellular immunity.
本项目旨在研究白细胞介素-12(IL-12)基因修饰的乳腺肉瘤小鼠细胞系EMT6/IL-12在小鼠模型中的抗肿瘤作用。在本研究中,我们将编码IL-12基因的重组真核质粒(pcDNA6-p70)转染至EMT6细胞中,获得了表达IL-12的EMT6/IL-12细胞系。然后将EMT6/IL-12细胞皮下接种到小鼠体内。将重组载体处理组设为对照组。接着我们在体内评估了肿瘤生长抑制情况以及抗肿瘤免疫功能,如细胞毒性、脾细胞增殖和系列干扰素-γ水平。并且还分析了荷瘤小鼠脾细胞中产生干扰素-γ的CD4或CD8 T细胞的百分比。我们的结果表明,EMT6/IL-12组肿瘤生长明显受到抑制。此外,与对照组相比,EMT6/IL-12组的抗肿瘤免疫能力均显著更高。本研究结果支持EMT6/IL-12可通过增强抗肿瘤细胞免疫在肿瘤模型中发挥基因治疗作用这一观点。