Identification of Two Novel HLA-A*0201-Restricted CTL Epitopes Derived from MAGE-A4

被引:14
作者
Jia, Zheng-Cai [1 ]
Ni, Bing [1 ]
Huang, Ze-Min [1 ]
Tian, Yi [1 ]
Tang, Jun [2 ]
Wang, Jing-Xue [1 ]
Fu, Xiao-Lan [1 ]
Wu, Yu-Zhang [1 ]
机构
[1] Third Mil Med Univ, Dept Immunol, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Southwest Hosp, Dept Dermatol, Chongqing 400038, Peoples R China
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2010年
关键词
CYTOLYTIC T-LYMPHOCYTES; TUMOR-ASSOCIATED ANTIGEN; CANDIDATE PROTEINS GP100; CANCER-TESTIS ANTIGENS; CLASS-I MOLECULES; GENE-EXPRESSION; HETEROGENEOUS EXPRESSION; CANCER/TESTIS ANTIGENS; CELL RECOGNITION; PEPTIDE BINDING;
D O I
10.1155/2010/567594
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
MAGE-A antigens belong to cancer/testis (CT) antigens that are expressed in tumors but not in normal tissues except testis and placenta. MAGE-A antigens and their epitope peptides have been used in tumor immunotherapy trials. MAGE-A4 antigen is extensively expressed in various histological types of tumors, so it represents an attractive target for tumor immunotherapy. In this study, we predicted HLA-A*0201-restricted cytotoxic T lymphocyte (CTL) epitopes of MAGE-A4, followed by peptide/HLA-A*0201 affinity and complex stability assays. Of selected four peptides (designated P1, P2, P3, and P4), P1 (MAGE-A4(286-294), KVLEHVVRV) and P3 (MAGE-A4(272-280), FLWGPRALA) could elicit peptide-specific CTLs both in vitro from HLA-A*0201-positive PBMCs and in HLA-A*0201/K-b transgenic mice. And the induced CTLs could lyse target cells in an HLA-A*0201-restricted fashion, demonstrating that the two peptides are HLA-A*0201-restricted CTL epitopes and could serve as targets for therapeutic antitumoral vaccination.
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页数:7
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