Identification of novel helper epitope peptides of Survivin cancer-associated antigen applicable to developing helper/killer-hybrid epitope long peptide cancer vaccine |
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Authors: | Junya Ohtake Takayuki Ohkuri Yuji Togashi Hidemitsu Kitamura Kiyotaka Okuno Takashi Nishimura |
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Affiliation: | 1. Division of Immunoregulation, Section of Disease Control, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan;2. Bioimmulance Co. Ltd., Sapporo, Japan;3. Department of Surgery, Kinki University, Faculty of Medicine, Osaka-Sayama, Japan;4. Division of ROYCE’ Health Bioscience, Section of Disease Control, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan |
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Abstract: | We identified novel helper epitope peptides of Survivin cancer antigen, which are presented to both HLA-DRB1*01:01 and DQB1*06:01. The helper epitope also contained three distinct Survivin-killer epitopes presented to HLA-A*02:01 and A*24:02. This 19 amino-acids epitope peptide (SU18) induced weak responses of Survivin-specific CD4+ and CD8+ T cells though it contained both helper and killer epitopes. To enhance the vaccine efficacy, we synthesized a long peptide by conjugating SU18 peptide and another DR53-restricted helper epitope peptide (SU22; 12 amino-acids) using glycine-linker. We designated this artificial 40 amino-acids long peptide containing two helper and three killer epitopes as Survivin-helper/killer-hybrid epitope long peptide (Survivin-H/K-HELP). Survivin-H/K-HELP allowed superior activation of IFN-γ-producing CD4+ Th1 cells and CD8+ Tc1 cells compared with the mixture of its component peptides (SU18 and SU22) in the presence of OK-432-treated monocyte-derived DC (Mo-DC). Survivin-H/K-HELP-pulsed Mo-DC pretreated with OK-432 also exhibited sustained antigen-presentation capability of stimulating Survivin-specific Th1 cells compared with Mo-DC pulsed with a mixture of SU18 and SU22 short peptides. Moreover, we demonstrated that Survivin-H/K-HELP induced a complete response in a breast cancer patient with the induction of cellular and humoral immune responses. Thus, we believe that an artificially synthesized Survivin-H/K-HELP will become an innovative cancer vaccine. |
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Keywords: | CTL, cytotoxic T lymphocytes EBV-B, Epstein&ndash Barr virus-transformed B H/K-HELP, helper/killer-hybrid epitope long peptide HPV, human papilloma virus MMC, mitomycin C Mo-DC, monocyte-derived dendritic cells PBMC, peripheral blood mononuclear cells SLP, synthetic long peptide Tc, cytotoxic T Th, helper T Treg, regulatory T |
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