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树突状细胞与髓性白血病的免疫治疗 *
引用本文:陈 莉,楼国良.树突状细胞与髓性白血病的免疫治疗 *[J].中国肿瘤生物治疗杂志,2000,7(1):69-70.
作者姓名:陈 莉  楼国良
作者单位: 
基金项目: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,B-7和GM-CSF表达载体,以研究基因修的肿瘤细胞的癌疫苗作用。方法:将3种表达载体分别转染EL-4胞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:当接种子EL4/IL-12细胞后,在C57PL/6同系鼠中其基因导入细胞的肿瘤原性比较EL4/Wt和EL-4/Neo组明显减少(P〈0.01)。在EL4/IL-12被排斥后,体内试验中诱发了实验动物抗

关 键 词:IL-12  B7-1  GM-CSF  基因治疗  癌症  小鼠
收稿时间:3/1/1999 12:00:00 AM
修稿时间:1999/5/20 0:00:00

IL-12 Synergizes B7-1 Enhance the Antitumor Immunity in Experimental Mice
Chen Li and Lou Guoliang.IL-12 Synergizes B7-1 Enhance the Antitumor Immunity in Experimental Mice[J].Chinese Journal of Cancer Biotherapy,2000,7(1):69-70.
Authors:Chen Li and Lou Guoliang
Abstract: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.
Keywords:IL-12  B7-1  GM-CSF  cancer vaccine  gene therapy
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