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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.
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页码:329 / 336
页数:8
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