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出 处:《中华肿瘤杂志》2007年第11期M0004-M0004,共1页Chinese Journal of Oncology
摘 要:Synthetic peptides representing epitopes for antigen-specific CTL have been considered as prime candidates for vaccine development. However, in vivo administration of the peptides can activate T-cell response in some cases but can induce T-cell tolerance in others. The outcome of the CTL response to a peptide challenge is dictatedSynthetic peptides representing epitopes for antigen-specific CTL have been considered as prime candidates for vaccine development. However, in vivo administration of the peptides can activate T-ceU response in some cases but can induce T-cell tolerance in others. The outcome of the CTL response to a peptide challenge is dictated in great part by the activation status of antigen-presenting cell (APC). In the activation of APC, such as dendritic cells (DC), the Toll-like receptor (TLR) plays an important role. Ligation of TLRs by relevant ligands leads to significant enhancement of the antigen-presenting capacity of DC to naive CTL. The mechanism consists of increase in a) expression of peptide/MHC complexes, b) expression of co-stimulatory molecules ( CD80/86 ) and c ) cytokine secretion ( IL-12, IFN-α). E. Celis in a recent paper ( Cancer Res, 2007, 67 : 7945-7947 ) reviewed the research of his group on the use of synthetic oligodeoxynucleotides containing CpG motifs which activate DC by ligation to TLR-9 in the treatment of cancer.
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