Prostate-specific antigen-derived epitopes capable of inducing cellular and humoral responses in HLA-A24+ prostate cancer patients

被引:42
作者
Harada, M
Kobayashi, K
Matsueda, S
Nakagawa, M
Noguchi, M
Itoh, K
机构
[1] Kurume Univ, Sch Med, Dept Immunol, Kurume, Fukuoka 8300011, Japan
[2] Kurume Univ, Sch Med, Dept Urol, Kurume, Fukuoka 8300011, Japan
关键词
prostate cancer; cytotoxic T lymphocytes; PSA; HLA-A24; peptide; antibody;
D O I
10.1002/pros.10280
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. We tried to identify prostate-specific antigen (PSA)-derived epitopes immunogenic in HLA-A24(+) prostate cancer patients. METHODS. Peripheral blood mononuclear cells (PBMCs) were in vitro stimulated with each of four different PSA peptides carrying the HLA-A24 binding motif, and their HLA-A24-restricted anti-tumor responses were examined using a parental HLA-A24-negative prostate cancer cell line (PC93) and its HLA-A24-expressing transfectant line (PC93-A24). Serum levels of immunoglobulin G (IgG) against PSA peptides were measured by enzyme-linked immunosorbent assay (ELISA). RESULTS. PBMCs, which were in vitro stimulated with either the PSA(152-160) or PSA(248-257) peptide, showed higher levels of IFN-gamma production and cytotoxicity against the PC93-A24 than against the PC93. IgG against the PSA(248-257) peptide was detected in half of the prostate cancer patients tested. CONCLUSIONS. The PSA(152-160) and PSA(248-257) peptides could be appropriate target molecules in use for specific immunotherapy of HLA-A24(+) prostate cancer patients. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:152 / 159
页数:8
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