Characterization of B16 melanoma-specific cytotoxic T lymphocytes |
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Authors: | Mamoru Harada Koji Tamada Koichiro Abe Tieli Li Yasuhiro Onoe Hitoshi Tada Katsunori Tatsugami Takashi Ando Genki Kimura Kikuo Nomoto |
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Affiliation: | (1) Department of Virology, Medical Institute of Bioregulation, Kyushu University, Fukuoka 812, Japan, JP;(2) Department of Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka 812, Japan, JP;(3) Internal Medicine II, Kyushu University, Fukuoka 812, Japan, JP |
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Abstract: | A B16 melanoma-specific CD8+ T cell line (AB1) was established from the spleen cells of C57BL/6 mice cured of B16 melanoma with interleukin (IL)-12 treatment. The AB1 line exclusively used T cell receptor Vβ11. The AB1 cells exhibited a cytolytic activity against both syngeneic B16 melanoma and allogeneic P815 mastocytoma, whereas a cold inhibition assay revealed specificity of the AB1 cells against B16 melanoma. Their lostability to kill a class I loss variant of B16 melanoma was restored by the transfection of H-2Kb gene. In addition, their interferon (IFN)-γ production was significantly suppressed by the addition of anti-H-2Kb monoclonal antibody, and RT-PCR analysis showed that the AB1 line expressed the mRNA encoding IFN-γ, but not IL-4 or IL-10. The experiment using synthetic peptides of tyrosinase-related protein-2 (TRP-2) revealed that the AB1 cells could recognize TRP-2181–188 peptide. Moreover, the AB1 cells showed an in vivo antitumor effect against established pulmonary metastases of B16 melanoma. Overall, these results indicate that the Tc1-type Vβ11 + AB1 cells exert an antitumor activity against syngeneic B16 melanoma through recognition of TRP-2181–188 peptide in an H-2Kb-restricted manner. Received: 4 June 1998 / Accepted: 21 July 1998 |
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Keywords: | B16 melanoma Cytotoxic T-lymphocytes Tc1 Tyrosinase-related protein-2 |
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