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作 者:王志华[1] 滕静[2] 谷宪三朗[3] 浅野茂隆[3]
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,哈尔滨市150040 [2]黑龙江省社会康复医院 [3]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:《中国肿瘤临床》2001年第9期696-699,共4页Chinese Journal of Clinical Oncology
基 金:黑龙江省自然科学基金资助(编号:D9518)
摘 要:目的:应用逆转录病毒构建IL-12、B7-1表达载体,以研究基因修饰的肿瘤细胞的癌疫苗作用。方法:将两种表达载体分别转染EL-4胸腺瘤细胞,使该细胞能表达分泌B7-1或IL-12,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转染细胞后,在C57BL/6同系鼠中其基因导入细胞的肿瘤原性比较EL-4/Wt和EL-4/Neo组明显减少(P<0.01),在EL-4/IL-12组的肿瘤被排斥后,实验动物体内诱发了抗EL-4/Wt的全身性、保护性免疫,用51Cr释放测定法证明有一个较强的抗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与CD4+、CD8+和NK细胞有关。用EL-4/IL-12基因转染的瘤细胞进行疫苗治疗比较用EL-4/Neo瘤细胞作疫苗治疗能更加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基因联合转染组比用单一的转基因细胞增强了治疗效果(P<0.005)。结论:研究结果提示应用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有一定的应用前景。Objective: To study the vaccine potency of gene-modified tumor cells, we have constructed IL-12, B7-1 expression vector using retrovirus. Methods: The two expression vectors were transfected into EL-4 thymic lymphoma cells and the effect of gene transduction on antitumor immunity were studied. Results: The tumorigenicity of EL-4/IL-12 transfectant in C57BL/6 synergisstical mice decreased significantly after implantation of EL-4/IL-12 transfectant as compaired with EL-4/Wt or EL-4/Neo groups(P<0.01). The systemic protective immunity was induced against the chanllenge with EL-4/Wt (in10/15 mice) after the rejection of EL-4/IL-12. In vivo experiment, a stronger CTL activity against EL-4/Wt cells and a weak killer activity against synergeneic Lewis lung carcinoma cells were obtained in 51Cr release assay. In vivo, the 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 of established EL-4/Wt tumors significantly as compaired with those of EL-4/Neo (P<0.005). Combination use of the therapeutic vaccines of EL-4/IL-12 and EL-4/B7-1 resulted in enhancing the therapeutic effect of each single transfectant in this experimental model (P<0.005). Conclusion: These studies suggested that immune treatment using IL-12 is effective in hematopoietic malignancy, and conbination of IL-12 and B7-1 may be of value in human cancer treatment.
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