scholarly journals An effective dendritic cell‐based vaccine containing glioma stem‐like cell lysate and CpG adjuvant for an orthotopic mouse model of glioma

2019 ◽  
Vol 144 (11) ◽  
pp. 2867-2879 ◽  
Author(s):  
Shan Zhu ◽  
Xinping Lv ◽  
Xuhao Zhang ◽  
Tete Li ◽  
Guoxia Zang ◽  
...  

2015 ◽  
Vol 11 (4) ◽  
pp. 922-930 ◽  
Author(s):  
Kenneth E Ugen ◽  
Xiaoyang Lin ◽  
Ge Bai ◽  
Zhanhua Liang ◽  
Jianfeng Cai ◽  
...  


Cytotherapy ◽  
2013 ◽  
Vol 15 (4) ◽  
pp. S35
Author(s):  
W. Ng ◽  
M. Abdullah ◽  
P. Chong ◽  
C. Leong ◽  
S. Fadilah ◽  
...  




2019 ◽  
Vol 21 (Supplement_6) ◽  
pp. vi158-vi158
Author(s):  
Sol Hooy Oh ◽  
Stephen Ahn ◽  
Jae Sung Park ◽  
Yong Kil Hong ◽  
Sin-Soo Jeon

Abstract BACKGROUND Dendritic cell (DC)-based vaccines have been suggested as one of the promising immunotherapies for treating various cancers, including glioblastoma. We already developed a novel vaccination protocol with peptide-loaded DCs followed by a mixture of synthetic peptides, polyinosine- polycytidylic acid (poly-IC) and anti-CD40 antibodies (Trivax) in a melanoma mouse model. However, in a glioma mouse model, therapeutic efficacy is not as much as enough maybe due to relatively low antigenicity and blood brain barrier. MATERIAL AND METHODS IL-7, which is one of the most important cytokines to expand and develop T cells with anti-tumor immunity, was co-administrated intravenously with Trivax in an orthotopic murine malignant glioma. RESULTS Co-administration of the Trivax and recombinant IL-7 (Trivax7) increased the number of survivin specific T cells measured using ELISPOT assay and the population of central memory T cells, comparing with administration of Trivax. The tumor size of orthotopic mouse model in Trivax 7 group was smaller than those of Trivax only group. Finally, overall survival in Trivax 7 was longer than those of Trivax only. In addition, there was a prolonged survival of antigen-specific T cells in Trivax7 group than Trivax only group. CONCLUSION In summary, our novel combinational immunotherapy may overcome the limitations of current cell-based cancer vaccines and could be applicable for the treatment of glioblastoma patients.





2014 ◽  
Vol 16 (suppl 5) ◽  
pp. v111-v111
Author(s):  
M. Dey ◽  
A. Chang ◽  
D. Wainwright ◽  
A. Ahmed ◽  
Y. Han ◽  
...  


2012 ◽  
Vol 77 (5-6) ◽  
pp. 633-635 ◽  
Author(s):  
Ichiro Nakano ◽  
E. Antonio Chiocca


PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e77019 ◽  
Author(s):  
Osamu Togao ◽  
Chase W. Kessinger ◽  
Gang Huang ◽  
Todd C. Soesbe ◽  
Koji Sagiyama ◽  
...  


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