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Clinical Cancer Research Vol. 7, 3950-3962, December 2001
© 2001 American Association for Cancer Research


Clinical Trials

Induction of Cellular Immune Responses to Tumor Cells and Peptides in Colorectal Cancer Patients by Vaccination with SART3 Peptides1

Yoshiaki Miyagi2, Nobue Imai2, Teruo Sasatomi, Akira Yamada, Takashi Mine, Kazuko Katagiri, Masami Nakagawa, Akira Muto, Shinya Okouchi, Hiroharu Isomoto, Kazuo Shirouzu, Hideaki Yamana and Kyogo Itoh3

Departments of Surgery [Y. M., T. S., T. M., H. I., K. S., H. Y.] and Immunology [N. I., A. Y., K. K., A. M., S. O., K. I.], Kurume University School of Medicine, and Cancer Vaccine Development Division, Research Center for Innovative Cancer Therapy [A. Y., M. N., K. I.], Kurume University, 830-0011 Fukuoka, Japan

The tumor-rejection antigen SART3 possesses two antigenic epitopes (SART3109–118 and SART3315–323) capable of inducing HLA-A24-restricted and tumor-specific CTLs. To determine its safety and ability to generate antitumor immune responses, 12 patients with advanced colorectal cancer were administered s.c. vaccinations of these peptides. No severe adverse events were associated with the vaccinations. Significant levels of increased cellular immune responses to both HLA-A24+ colon cancer cells and the vaccinated peptide were observed in the postvaccination peripheral blood mononuclear cells in 7 of 11 and 7 of 10 patients tested, respectively, and the higher responses were observed in those patients vaccinated with the highest dose (3 mg/injection) of the peptides. These results encourage further development of SART3 peptide vaccine for colorectal cancer patients.




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Copyright © 2001 by the American Association for Cancer Research.