前列腺癌
细胞毒性T细胞
外周血单个核细胞
抗原
肽
CD8型
癌症研究
人类白细胞抗原
免疫疗法
免疫学
医学
前列腺
癌症
免疫系统
生物
体外
内科学
生物化学
作者
Satoko Matsueda,Akihisa Yao,Yuki Ishihara,Rika Ogata,Masanori Noguchi,Kyogo Itoh,Mamoru Harada
出处
期刊:The Prostate
[Wiley]
日期:2004-02-02
卷期号:60 (3): 205-213
被引量:23
摘要
Abstract BACKGROUND We attempted to identify prostate stem cell antigen (PSCA)‐derived peptides immunogenic in HLA‐A24 + prostate cancer patients. METHODS Peripheral blood mononuclear cells (PBMCs) were stimulated in vitro with each of three different PSCA‐derived peptides, which were prepared based on the HLA‐A24 binding motif, and their peptide‐specific and HLA‐A24‐restricted anti‐tumor responses were examined. Plasma levels of immunoglobulin G (IgG) against PSCA peptides were measured by enzyme‐linked immunosorbent assay (ELISA). RESULTS Among three PSCA peptides, the PSCA 76–84 peptide most effectively induced peptide‐specific cytotoxic T lymphocytes (CTLs) from PBMCs of HLA‐A24 + prostate cancer patients. Cytotoxicity was dependent on peptide‐specific and CD8 + T cells. The PSCA 76–84 peptide‐stimulated PBMCs showed a significant level of cytotoxicity against prostate cancer cells in an HLA‐A24‐restricted manner. IgG reactive to the PSCA 76–84 peptide was detected in half of patients. CONCLUSIONS The PSCA 76–84 peptide should be considered for use in clinical trials of immunotherapy for HLA‐A24 + patients. © 2004 Wiley‐Liss, Inc.
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