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表达人IL-21的细胞因子诱导的杀伤细胞对裸鼠肝癌的治疗研究
陈晚华1,刘辉1,王延春2,朱洋洋2,曲平波1,钱其军1,2*
0
(1. 第二军医大学东方肝胆外科医院基因-病毒治疗实验室, 上海 200438
2. 浙江理工大学生命科学学院新元医学与生物技术研究所, 杭州 310018
*通信作者)
摘要:
目的 探讨细胞因子诱导的杀伤细胞(cytokine-induced killer cell,CIK细胞)作为人IL-21(hIL-21)基因的载体治疗肝癌的可行性。方法 构建携带hIL-21、CopGFP基因的质粒pDC759-hIL-21、 pDC759-CopGFP并分别与pAd5、pAd5F35共转染HEK293细胞,包装表达hIL-21、CopGFP蛋白的Ad5、Ad5F35病毒。分离培养CIK细胞并绘制生长曲线,将携带CopGFP基因的Ad5、Ad5F35病毒以不同MOI (0、1、5、10、50、100、1 000)感染CIK细胞;将携带hIL-21基因的Ad5、Ad5F35病毒以不同MOI (0、1、5、10、20、50)感染SMMC-7721细胞48 h后检测hIL-21蛋白的表达;将携带hIL-21基因的Ad5F35病毒以不同MOI (0、1、5、10、50、100)感染CIK细胞48 h后检测hIL-21蛋白的表达。皮下注射SMMC-7721细胞致裸鼠成瘤,以表达hIL-21的CIK细胞治疗荷瘤裸鼠,评价疗效。结果 成功构建出用于Ad5、Ad5F35病毒的质粒;构建的质粒与pAd5、pAd5F35脂质体共转染HEK293细胞,包装出表达hIL-21及CopGFP蛋白的Ad5、Ad5F35病毒。携带CopGFP基因的Ad5、Ad5F35病毒对CIK细胞的感染实验表明Ad5F35腺病毒感染率更高;携带hIL-21基因的Ad5、Ad5F35病毒对SMMC-7721细胞的感染实验表明hIL-21表达量差异无统计学意义;携带hIL-21基因的Ad5F35病毒以50 MOI感染CIK细胞后hIL-21的表达量较高;动物实验统计分析说明表达hIL-21的CIK细胞对荷瘤裸鼠疗效较好。结论 hIL-21与CIK细胞在荷瘤小鼠体内联合发挥抗肿瘤作用。
关键词:  白介素21  细胞因子诱的杀伤细胞  腺病毒  肝肿瘤
DOI:10.3724/SP.J.1008.2012.001045
投稿时间:2012-03-31修订日期:2012-08-29
基金项目:国家杰出青年科学基金(30925037).
Effect of cytokine-induced killer cells expressing hIL-21 on hepatocellular carcinoma in nude mice
CHEN Wan-hua1,LIU Hui1,WANG Yan-chun2,ZHU Yang-yang2,QU Ping-bo1,QIAN Qi-jun1,2*
(1. Laboratory of Viral and Gene Therapy, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China
2. Xinyuan Institute of Medicine and Biotechnology, School of Life Science, Zhejiang Sci-Tech University, Hangzhou 310018, Zhejiang, China
*Corresponding author.)
Abstract:
ObjectiveTo investigate the feasibility of using cytokine-induced killer (CIK) cells as targeted vehicle to deliver hIL-21 gene for hepatocellular carcinoma (HCC) treatment. MethodsWe constructed pDC759-hIL-21 and pDC759-CopGFP for cotransfection of HEK293 cells with pAd5 and pAd5F35 which can express hIL-21 and CopGFP proteins for viral packaging. We isolated CIK cells and plotted the growth curve. Then Ad5/AAV-CopGFP and Ad5F35/AAV-CopGFP of different MOIs (0,1,5,10,50,100, and 1 000) were used to infect CIK cells; Ad5/AAV-hIL-21 and Ad5F35/AAV-hIL-21 of different MOIs (0,1,5,10,20, and 50) were used to infect SMMC-7721 cells and the hIL-21 protein levels were examined by ELISA assay 48 h after infection. Ad5F35/AAV- hIL-21 of different MOIs (0, 1, 5, 10, 50, and 100) was used to infect CIK cells and hIL-21 protein levels were also examined 48 h after infection. SMMC-7721 cells were subcutaneously injected to nude mice for tumor forming, and then the tumor-bearing mice were treated with CIK cells carrying hIL-21 and the therapeutic effects were observed. ResultsPlasmids for viral packaging were constructed. After cotransfection of HEK293 cells, Ad5 and Ad5F35 which can express hIL-21 and CopGFP proteins were successfully packaged. Ad5 and Ad5F35 which can express CopGFP were used in this study. It was found that Ad5F35 was superior to Ad5 in CIK infection, with the suitable MOI being 50. Ad5/AAV-hIL-21 and Ad5F35/AAV-hIL-21 had similar effect on IL-21 expression in SMMC-7721 cells. Results of animal study showed that mice in group CIK/hIL-21 had a better curative effect. ConclusionhIL-21 and CIK cells have synergistic anti-tumor effect in nude mice bearing HCC.
Key words:  interleukin-21  cytokine-induced killer cell  adenovirus  liver neoplasms