Induction of human cytotoxic T lymphocytes by artificial antigen-presenting cells

被引:147
|
作者
Latouche, JB
Sadelain, M
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Human Genet, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Program Immunol, New York, NY 10021 USA
关键词
adoptive cell therapy; CD8(+) T cell; costimulation; dendritic cells; immunotherapy; retrovirus-mediated gene transfer;
D O I
10.1038/74455
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The adoptive transfer of antigen-specific cytotoxic T lymphocytes (CTLs) is a promising therapeutic approach for a number of diseases. To overcome the difficulty in generating specific CTLs, we established stable artificial antigen-presenting cells (AAPCs) that can be used to stimulate T cells of any patient of a given human leukocyte antigen (HLA) type. Mouse fibroblasts were retrovirally transduced with a single HLA-peptide complex along with the human accessory molecules B7.1, ICAM-1, and LFA-3. These AAPCs consistently elicit strong stimulation and expansion of HLA-restricted CTLs. Owing to the high efficiency of retrovirus-mediated gene transfer, stable AAPCs can be readily engineered for any HLA molecule and any specific peptide.
引用
收藏
页码:405 / 409
页数:5
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