Dendritic cells transfected with lentiviral vector-encoding human granulocyte-macrophage colony-stimulating factor augment anti-tumour T-cell response in vitro

被引:4
|
作者
Cui, J. [1 ]
Lin, A. L. [2 ]
Liu, Q. [1 ]
Sun, Q. [1 ]
Gao, Z. -H. [3 ,4 ]
机构
[1] Shandong Univ, Sch Med, Dept Pathol, Qian Fo Shan Hosp,Med Coll, Jinan 250014, Shandong, Peoples R China
[2] Third Peoples Hosp, Hangzhou, Zhejiang, Peoples R China
[3] Univ Calgary, Dept Pathol & Lab Med, Calgary, AB T2N 2T9, Canada
[4] Calgary Lab Serv, Calgary, AB T2N 2T9, Canada
关键词
MHC CLASS-I; GENE-TRANSFER; IFN-ALPHA; RECOMBINANT ADENOVIRUS; PANCREATIC-CANCER; TUMOR-ANTIGEN; IMMUNITY; EFFICIENT; TRANSDUCTION; INDUCTION;
D O I
10.1111/j.1744-313X.2010.00927.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
P>Dendritic cells (DC) are professional antigen-presenting cells that can actively taken up and present tumour-derived proteins to induce a tumour-specific immune response. Granulocyte-macrophage colony-stimulating factor (GM-CSF) plays a pivotal role in the generation, sensitization, maturation and survival of DC. We charged the peripheral blood monocyte cell-derived DC with tumour lysate, and then transfected the DC with lentiviral vector-encoding human GM-CSF (hGM-CSF). The antigen-presenting capacity of the hGM-CSF-transfected DC was tested by means of the mixed lymphocyte reaction and cytotoxic T-lymphocyte assay using wild-type DC as the control. The Lenti-hGM-CSF-transfected DC was able to stimulate the proliferation of naive allogeneic T lymphocytes and to generate tumour-specific cytotoxic T lymphocytes more efficiently than the wild-type DC. This data indicates that Lenti-hGM-CSF-transfected DC could potentially be used as an effective clinical approach for cancer immunotherapy.
引用
收藏
页码:329 / 336
页数:8
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