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作 者:孙文长[1] 唐展云[1] 魏道严[1] 汤宇澄[1] 陈诗书[1]
机构地区:[1]第二医科大学生物化学教研室人类基因治疗研究中心,上海200025
出 处:《中华肝脏病杂志》2001年第5期300-302,共3页Chinese Journal of Hepatology
基 金:国家自然科学基金(39730440)
摘 要:目的 观察白介素18和胞嘧啶脱氨酶基因对小鼠肝癌MM45T.Li联合基因治疗的效果。 方法 将小鼠IL-18基因克隆入pGCEN中,构建成pGCEN/IL-18。包装成逆转录病毒,感染小鼠肝癌细胞MM45T.Li, 制出具有生物活性的MM45T.Li/IL-18瘤苗,灭活后对荷瘤小鼠进行皮下接种。同时利用AdCD/5FC对小鼠肝癌原位注射,进行联合基因治疗。 结果 在接受治疗30d后,MM45T.Li对照组肿瘤体积1580~1625mm3,MM45T.Li/IL-18治疗组(366±159)mm3,AdCD/5FC治疗组(438±65)mm3,IL-18和AdCD/5FC联合治疗组体积(15±7)mm3(P<0.05)。MM45T.Li对照组中位生存期50.0~51.5d,MM45T.Li/IL-18治疗组65d,AdCD/5FC治疗组57d,联合治疗组76d,和单独治疗组相比,联合治疗组中位生存期明显延长(P<0.05)。联合基因治疗组肿瘤组织周围有更多CD4+及CD8+淋巴细胞浸润。 结论 IL-18和CD基因的联合治疗组,其疗效要明显好于IL-18或CD基因单独治疗组。进行联合基因治疗,既有效地减少了肿瘤负荷,又充分调动了机体的抗肿瘤免疫,提高了疗效。Objective To investigate the synergistic antitumor effects of murine IL-18 and CD/5FC gene therapy on mice bearing liver cancer. Methods A retrovirus vector pGCEN/IL-18 containing murine interleukin-18 gene was constructed. The retrovirus carrying IL-18 gene was used to infect murine liver cancer cell MM45T.Li , and proved to secret biological active IL-18. In mice bearing liver cancer, 60Co-irradiated MM45T.Li/IL-18 vaccine was inoculated subcutaneously once a week for two weeks, and/or AdCD was injected intratumorally with 5FC injected i.p. for 8 days. Results Thirty days from the treatment, the tumor volume of control group was 1580~1625mm3, MM45T.Li/IL-18 vaccine group was 366±159mm3, AdCD/5FC group was 438±65mm3, and combined IL-18 and AdCD/ 5FC therapy group was 15±7 mm3(P<0.05). The tumor volume in single gene therapy group reduced to the smallest after three-week treatment, but grew large again, while the tumor volume in combined therapy group still remained small. The median survival time in control group was 50.0~51.5 days, MM45T.Li/IL-18 group was 65 days, AdCD/5FC group was 57 days versus 75 days for combined gene therapy group (P<0.05), and with more abundant infiltration of CD4+ and CD8+ lymphocytes around the tumor in combined gene therapy group. Conclusions Combined gene therapy with IL-18 and CD/5FC can reduce the tumor volume and elicit the antitumor immunity of the host, which is superior to the single gene therapy for murine liver cancer. [
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