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作 者:王志华[1] 康熙雄[1] 谷宪三朗[2] 住本秀敏[2] 中畸有恒[2] 浅野茂隆[2]
机构地区:[1]哈尔滨医科大学肿瘤研究所分子生物与基因工程研究室,哈尔滨150040 [2]日本东京大学医科学研究所病态药理/分子治疗研究部门
出 处:《中国肿瘤生物治疗杂志》2000年第1期46-49,共4页Chinese Journal of Cancer Biotherapy
基 金:黑龙江省自然科学基金!(D9518)资助
摘 要:目的:我们应用逆转录病毒构建了IL-12,R7-1和GM-CSF表达载体,以研究基因修饰的肿瘤细胞的癌疫苗作用。方法:将3种表达载体分别转染EM胸腺瘤细胞并研究了该基因导入细胞的抗肿瘤免疫效果。结果:当接种了EL-4/IL-12细胞后,在C57BL/6同系鼠中其基因导入细胞的肿瘤原性比较EL-4和EL-4/Neo组明显减少(P<0.01)。在EL-4/IL-12被排斥后,体内试验中诱发了实验动物抗 EL-4/Wt的系统性、保护性免疫,51Cr释放测定中,获得一个较强的抗EL-4/Wt和一个较弱的抗同系Lewis肿瘤细胞的CTL活性,体内淋巴细胞消除分析的结果提示减少的肿瘤原性主要依赖于CD4+,CD8+和NK细胞。用EL-4/IL-12细胞进行疫苗治疗比较用EL-4/Neo细胞能有效地延缓已建立的EL-4/Wt肿瘤的生长(P<0.005),EL-4/IL-12和EL-4/B7-1联合比用单一的转基因细胞增强了治疗效果(P<0.005)。结论:提示应用IL-12进行血液肿瘤的治疗是有效的,IL-12和B7-1联合使用在未来人类癌症的治疗中亦可有一定的应用前景。Objective: To study the vaccine potency of gene-modified tumor cells, we have constructed IL-12, H7-1 and GM-CSF express vector using retrovirus. Methods: It was transfected into EL-4 thymic lylmphoma cells respectively and the effect of gene transduction on anti-tumor immunity were investigated. Results: The tumorigenicity of EL-4/IL-12 transfectant in C57BI/6 syn- ergistical mice was decreased significantly after implanted with EL-4/IL-12 transfectant compaired with EL-4/Wt or EL-4/Neo groups (P<0. 01). The systemic protective immunity was induced against the challenge with EL-4/Wt (in 10/15 mice) after the rejection of EL-4/IL-12 in the experiment, a stronger CTL activity against EL-4/Wt cells and a weak killer activity against syn- geneic Lewis Lung Carcinoma cells were obtained in 51Cr release assay. In vivo depletion analysis suggested that the decreased tumorigenicity mainly depended on CD4+, CD8+ and NK cells. Therapeutic vaccines with EL-4/IL-12 cells could retard the growth to estabished EL-4/Wt tumors significantly compared with those of EL-4/Neo(P < 0 .005 ), combination of therapeutic vaccines of EL-4/IL-12 and EL-4/B7-1 result in the enhanced the therapeutic effect of each single transficants (P < 0 .005) in this experimental model. Conclution: These studies suggested that immunogene treatment using IL-12 is effective in hematopoi- etic malignancy, and combination of IL-12 with B7-1 have a aplication value in human cancer treatment in the near future.
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