Author/Authors :
Pourgholaminejad، نويسنده , , Arash and Jamali، نويسنده , , Arezoo and Samadi-Foroushani، نويسنده , , Morteza and Amari، نويسنده , , Afshin and Mirzaei، نويسنده , , Reza and Ansaripour، نويسنده , , Bita and Khansari، نويسنده , , Nemat and Aghasadeghi، نويسنده , , Mohammad Reza and Baban، نويسنده , , Babak and Hadjati، نويسنده , , Jamshid، نويسنده ,
Abstract :
CpG motifs have been advanced as agents that stimulate the maturation of DCs for immunotherapy. The present study tested the hypothesis that multiple doses of CpG-matured DC vaccine would be efficacious for complete eradication of experimentally-induced tumor. Accordingly, WEHI164 cells were implanted subcutaneously in the flank of BALB/c mice. During DC culture, tumor lysate was added to immature DCs followed by addition of CpG or non-CpG control 4–6 h later. A total of three doses of CpG or non-CpG control-matured DCs were injected around tumors. The results showed that multiple doses of CpG-matured DCs led to considerable decrease in cytotoxicity of lymphocytes and significantly increased tumor growth rate compared to a single dose. Further, mice which received three doses of the vaccine also displayed significant FoxP3 in tumor tissue. In conclusion, multiple doses of CpG-matured DCs exhibited decreased anti-tumor immunity in association with increased expression of FoxP3.
Keywords :
cell therapy , Synthetic oligodeoxynucleotides , tumor immunotherapy , FoxP3