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通过树突状细胞与工程化肿瘤细胞融合进行免疫接种增强抗肿瘤作用。

Enhancing antitumor by immunization with fusion of dendritic cells and engineered tumor cells.

作者信息

Zhang Weidong, Yang Hong, Zeng Hongtao

机构信息

Department of Microbiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2002;22(1):1-4. doi: 10.1007/BF02904773.

Abstract

A novel approach for a dentritic cells (DCs)-based tumor vaccine was developed for the formation of hybrid-engineered J558 after fusion with DCs. To make the hybrid-tumor vaccine generate more efficient specific CTL cytotoxicity against wild-type tumor cells, we genetically engineered tumor cells with mIL-12 gene prior to the cell fusion. mIL-12 was detected at 870 +/- 60 pg/(10(5) cells/ml) in the culture supernatants and the fusion ratio was about 30% by the co-focal microscopic analysis. Vaccination of mice with DCs fused with engineered J558 induced more efficient tumor-specific CTL cytotoxicity against wild-type tumor cells in vitro and with efficient antitumor immunity in vivo. These results suggest that this approach of using DCs fused with engineered tumor cells could be applied in clinical settings of DCs-based cancer vaccines.

摘要

开发了一种基于树突状细胞(DCs)的新型肿瘤疫苗方法,用于在与DCs融合后形成杂交工程化J558。为了使杂交肿瘤疫苗对野生型肿瘤细胞产生更有效的特异性CTL细胞毒性,我们在细胞融合前用mIL-12基因对肿瘤细胞进行基因工程改造。通过共聚焦显微镜分析,在培养上清液中检测到mIL-12的含量为870±60 pg/(10⁵个细胞/ml),融合率约为30%。用与工程化J558融合的DCs对小鼠进行疫苗接种,在体外诱导了对野生型肿瘤细胞更有效的肿瘤特异性CTL细胞毒性,并在体内诱导了有效的抗肿瘤免疫。这些结果表明,这种使用与工程化肿瘤细胞融合的DCs的方法可应用于基于DCs的癌症疫苗的临床应用。

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