International Journal of Cancer · 1999 · 56 citations · 24 references
Life SciencesImmunologyOncologyCancer ImmunologyImmunotherapyTumor ImmunologyAntigen RecognitionAntitumor T Cell ResponsesCancer ImmunotherapyImmunotherapy For Brain TumorsT Cell Responses To TumorsTumor AntigensAntigen Recognition By Cytotoxic T LymphocytesCancer AntigensClass I Histocompatibility AntigensHla Antigen ExpressionPeptide Antigen RecognitionTumor Antigen RecognitionTumor Antigen-based ImmunotherapyTumor Rejection Antigens
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.
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A Gene Encoding an Antigen Recognized by Cytolytic T Lymphocytes on a Human Melanoma
Pierre van der Bruggen, Catia Traversari, Patrick Chomez et al. · Science · 1991 · 3.5K citations
Life Sciences, Immunology, Oncology +17
Vaccination of melanoma patients with peptide- or tumorlysate-pulsed dendritic cells
Frank O. Nestlé, Selma Alijagic, Michel Gilliet et al. · Nature Medicine · 1998 · 2.9K citations
Medicine, Immunology, Oncology +14
Yutaka Kawakami, S Eliyahu, Kazuyasu Sakaguchi et al. · The Journal of Experimental Medicine · 1994 · 865 citations · Full text
Life Sciences, Immunology, Oncology +17