| Literature DB >> 10597192 |
T Imaizumi1, T Kuramoto, K Matsunaga, S Shichijo, S Yutani, M Shigemori, K Oizumi, K Itoh.
Abstract
We have reported a tumor-rejection antigen, SART1(259), possessing tumor epitopes capable of inducing cytotoxic T lymphocytes (CTLs) in epithelial-cancer patients. This study investigated the expression of SART1(259) antigen in brain tumors, to explore for a potential molecule for use in specific immunotherapy of patients with brain tumors. The SART1(259) antigen was detected in the cytosol fraction of 13 of 18 (72%) glioma cell lines and in 12 of 34 (35%) brain-tumor tissues, with a higher rate of expression among malignant gliomas (5/10, 50%) and schwannomas (3/4). HLA-A24-restricted and SART1-specific CTLs recognized the HLA-A24+ and SART1(259)+ glioma cells, and the levels of recognition correlated both with HLA-A24-antigen expression level and with the concentration of the SART1 peptide antigen. Therefore, the SART1(259) antigen could be a target molecule for specific immunotherapy of patients with brain tumors expressing HLA-class-1 antigens.Entities:
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Year: 1999 PMID: 10597192 DOI: 10.1002/(sici)1097-0215(19991210)83:6<760::aid-ijc11>3.0.co;2-r
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396