The CD133+ tumor stem-like cell-associated antigen may elicit highly intense immune responses against human malignant glioma

被引:31
作者
Hua, Wei [1 ]
Yao, Yu [1 ]
Chu, Yiwei [2 ]
Zhong, Ping [1 ]
Sheng, Xiaofang [3 ]
Xiao, Baoguo [4 ]
Wu, Jingsong [1 ]
Yang, Bojie [1 ]
Mao, Ying [1 ]
Zhou, Liangfu [1 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Neurosurg, Shanghai 200040, Peoples R China
[2] Fudan Univ, Shanghai Med Sch, Dept Immunol, Shanghai 200032, Peoples R China
[3] Shanghai Gamma Knife Hosp, Dept Radiotherapy, Shanghai 200235, Peoples R China
[4] Fudan Univ, Inst Neurol, Huashan Hosp, Shanghai 200040, Peoples R China
关键词
Malignant gliomas; Stem-like cell-associated antigens; Dendritic cells; Immunotherapy; IDENTIFICATION; VACCINATION; EXPRESSION; TARGET; LINES;
D O I
10.1007/s11060-011-0572-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To explore the immunogenicity of glioma stem-like cell-associated antigens (SAAs) from sorted or unsorted glioma tumor stem-like cells (TSCs) as well as irradiated TSCs. Two primary human malignant glioma lines (SHG62, SHG66) and U87 cell line were primarily cultured in the serum-free medium (SFM) supplemented with EGF/bFGF. TSCs were identified by their self-renewal, multi-lineage differentiation and tumorigenic activity. To prepare SAAs in vitro, CD133+ TSCs were sorted either by magnetic cell sorting or with irradiation (6 Gy).The cytotoxicity induced by autogenous myeloid dendritic cell (DC)-mediated SAA-specific cytotoxic T lymphocytes (CTLs) was assessed by the Just Another Method test. SHG62, SHG66, and U87 cells contained TSCs. CD133+ SAAs-specific CTLs were significantly more cytotoxic than effector cells loaded with unsorted SAA (P < 0.05). Effector cells loaded with irradiated SAAs were more cyotoxic than those with regular SAAs (P < 0.01). SAAs from CD133+ TSCs and irradiated TSCs provide highly immunogenic antigens. TSCs might be a novel source of antigens for DC vaccination against malignant gliomas.
引用
收藏
页码:149 / 157
页数:9
相关论文
共 27 条
[21]   Identification of human brain tumour initiating cells [J].
Singh, SK ;
Hawkins, C ;
Clarke, ID ;
Squire, JA ;
Bayani, J ;
Hide, T ;
Henkelman, RM ;
Cusimano, MD ;
Dirks, PB .
NATURE, 2004, 432 (7015) :396-401
[22]  
WEI H, 2009, CHIN J NEUROSURG, V25, P847
[23]   Expression of MHC I and NK ligands on human CD133+ glioma cells:: possible targets of immunotherapy [J].
Wu, Anhua ;
Wiesner, Steve ;
Xiao, Jing ;
Ericson, Katya ;
Chen, Wei ;
Hall, Walter A. ;
Low, Walter C. ;
Ohlfest, John R. .
JOURNAL OF NEURO-ONCOLOGY, 2007, 83 (02) :121-131
[24]   Antigen-Specific T-Cell Response from Dendritic Cell Vaccination Using Cancer Stem-Like Cell-Associated Antigens [J].
Xu, Qijin ;
Liu, Gentao ;
Yuan, Xiangpeng ;
Xu, Minlin ;
Wang, Hongqiang ;
Ji, Jianfei ;
Konda, Bindu ;
Black, Keith L. ;
Yu, John S. .
STEM CELLS, 2009, 27 (08) :1734-1740
[25]   Transcriptional expression of survivin and its splice variants in brain tumors in humans [J].
Yamada, Y ;
Kuroiwa, T ;
Nakagawa, T ;
Kajimoto, Y ;
Dohi, T ;
Azuma, H ;
Tsuji, M ;
Kami, K ;
Miyatake, S .
JOURNAL OF NEUROSURGERY, 2003, 99 (04) :738-745
[26]   B7-H4 is preferentially expressed in non-dividing brain tumor cells and in a subset of brain tumor stem-like cells [J].
Yao, Yu ;
Wang, Xiaomei ;
Jin, Kunlin ;
Zhu, Jianhong ;
Wang, Yin ;
Xiong, Sidong ;
Mao, Ying ;
Zhou, Liangfu .
JOURNAL OF NEURO-ONCOLOGY, 2008, 89 (02) :121-129
[27]  
Yu JS, 2001, CANCER RES, V61, P842