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9220 ()2013 10 7 20 Chin J Clinicians(Electronic Edition),October 15,2013,Vol.7,No.20
MUC1-VNTRn
MUC1-VNTRn
pVAX1-MUC1-VNTRn pVAX1-MUC1-VNTRn
T ELISPOT IFN-γT CTL
CytoTox® MUC1-VNTRn CTL Capan-2
pVAX1-MUC1-VNTRn
pVAX1-MUC1-VNTRn
pVAX1-MUC1-VNTRn CD80
CD86HLA-DR IL-12 P 0.01
MUC1-VNTR MUC1-VNTR T IFN-γ T 103.08.5
6 9
94.37.7P 0.001MUC1-VNTR MUC1-VNTR CTL Capan-2
6 9
40.123.16%37.313.95%MUC1-VNTR VNTR VNTR VNTR MUC1-cDNA
1 1 3 4
P 0.001
pVAX1-MUC1-VNTR6 panc02-MUC1
pVAX1-MUC1-VNTR VNTR VNTR P 0.01 pVAX1-MUC1-VNTRn
1 3 9
pVAX1-MUC1-VNTR6
DNA CA-15-3
Optimized construction of MUC1-VNTRn DNA vaccine and the anti-pancreatic cancer research ZHOU
Quan-bo, GONG Yuan-feng, ZHOU Yu, LIN Qing, LI Zhi-hua, CHEN Ru-fu, ZENG Bing, ZHENG Li-ping.
Department of Hepatobiliary Surgery , The Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou
510120, China
Corresponding author: CHEN Ru-fu, Email: chenrf10@
Abstract Objective MUC1-VNTRn served as a new target for pancreatic cancer immunotherapy in the
present study. We intended to screen out the most powerful pVAX1-MUC1-VNTRn DNA vaccine which showed
strongest immunogenicity in vitro and vivo. Methods pVAX1-MUC1-VNTRn were constructed and transfected
into MUC1 negative cells. The target protein of MUC1-VNTRn could be detected by Western Blot. Dendritic cell
preparation and research of biological characteristics. p
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