Identification of peptides which can be applied to cancer vaccine therapy for patients with prostate cancer
Project/Area Number |
15K10612
|
Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Urology
|
Research Institution | Kindai University |
Principal Investigator |
|
Project Period (FY) |
2015-04-01 – 2018-03-31
|
Project Status |
Completed (Fiscal Year 2017)
|
Budget Amount *help |
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
|
Keywords | ペプチドワクチン / 前立腺癌 |
Outline of Final Research Achievements |
3~5 prostate cancer-associated antigens (PTH-rP,EGFR,EZH2) -derived peptides that were prepared based on the binding motif to the HLA-A3 supertype alleles (HLA-A11, -A31, and -A33) were functionally screened for their potential to induce peptide-specific cytotoxic T lymphocytes (CTLs) from peripheral blood mononuclear cells (PBMCs) of 12 HLA-A3 supertype allele+ prostate cancer patients. As a result, EZH2733-741 peptide was found to efficiently induce peptide-specific CTLs. To test cytotoxicity of CTLs by a standard 6-h 51Cr-release assay, CD8+ T cells were purified from EZH2733-741 peptide-stimulated PBMCs. The EZH2733-741 peptide-stimulated and purified CD8+ T cells from PBMCs of HLA-A3 supertype allele+ prostate cancer patients showed higher cytotoxicity against HLA-A3 supertype allele-expressing LNCaP prostate cancer cells than against parental LNCaP cells.
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Report
(4 results)
Research Products
(1 results)