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首页|期刊导航|中国肿瘤生物治疗杂志|EPHA2基因腺病毒感染树突状细胞诱导CTL对胶质瘤细胞的杀伤作用

EPHA2基因腺病毒感染树突状细胞诱导CTL对胶质瘤细胞的杀伤作用

陈宏颉 袁邦清 王守森 郑兆聪 高进喜 王如密

中国肿瘤生物治疗杂志2012,Vol.19Issue(1):35-39,5.
中国肿瘤生物治疗杂志2012,Vol.19Issue(1):35-39,5.DOI:10.3872/j.issn.1007-385X.2012.01.006

EPHA2基因腺病毒感染树突状细胞诱导CTL对胶质瘤细胞的杀伤作用

Cytotoxic effect of CTLs elicited by dendritic cells infected with adenovirus containing EPHA2 gene on glioma cells

陈宏颉 1袁邦清 2王守森 1郑兆聪 1高进喜 1王如密1

作者信息

  • 1. 南京军区福州总医院神经外科,福建福州 350000
  • 2. 南京军区福州总医院476医院神经外科,福建福州 350002
  • 折叠

摘要

Abstract

Objective;To explore the cytotoxic effect of cyctotoxic T lymphocytes (CTLs) induced by dendritic cells (DCs) modified by EPHA2 gene on U251 glioma cells, and to provide new ways for glioma immune therapy. Methods; DCs originated from the HLA-A2 + PBMCs were infected with recombinant adenovirus containing EPHA2 full length cDNA, and the DC vaccine modified by EPHA2 gene was prepared. The expression of EPHA on DCs was detected by Western blotting and FACS. HLA-A2 + PBMCs were stimulated by the DC vaccine in vitro. The specificity CTL activity induced by rAd-EPHA2-DCs and the cytotoxicity on HLA-A2 + U251 glima cells were detected by enzyme-linked immunospot assay (EliS-POT) and standard 51 Cr release experiment. Results: The DC vaccine modified by EPHA2 gene was successfully prepared, and EPHA2 protein was effectively expressed. Compared to DCs infected with rAd-LacZ and PBS groups, DCs infected with rAd-EPHA2 stimulated CTL activity effectively ([187 ±21] vs [12 ±4], [18 ±5]; P <0.01) and the CTLs induced by rAd-EPHA2-DCs produced cytotoxicity effect on U251 cells obviously ([45.7+6.8]% vs [7.1 ±4.5]%, P<0.01), and did not cause the cytotoxicity of its own lymphocytes. Conclusion; The DC vaccine modified by EPHA2 gene can stimulate the specificity CTL response effectively, and can cause cytotoxicity on glioma U251 cells obviously.

关键词

EPHA2基因/树突状细胞/胶质瘤

Key words

EPHA2 gene/ dendritic cell/ glioma

分类

医药卫生

引用本文复制引用

陈宏颉,袁邦清,王守森,郑兆聪,高进喜,王如密..EPHA2基因腺病毒感染树突状细胞诱导CTL对胶质瘤细胞的杀伤作用[J].中国肿瘤生物治疗杂志,2012,19(1):35-39,5.

基金项目

福建省自然科学基金资助项目(No.2006J0373) (No.2006J0373)

中国肿瘤生物治疗杂志

OA北大核心CSCDCSTPCD

1007-385X

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