Characterization of B16 melanoma-specific cytotoxic T lymphocytes

被引:17
作者
Harada, M
Tamada, K
Abe, K
Li, TL
Onoe, Y
Tada, H
Tatsugami, K
Ando, T
Kimura, G
Komoto, K
机构
[1] Kyushu Univ, Med Inst Bioregulat, Dept Virol, Fukuoka 812, Japan
[2] Kyushu Univ, Fukuoka 812, Japan
关键词
B16; melanoma; cytotoxic T-lymphocytes; Tcl; tyrosinase-related protein-2;
D O I
10.1007/s002620050521
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A Bid 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 V-beta 11. 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-2K(b) gene. In addition, their interferon production was significantly suppressed by the addition of anti-H-2K(b) monoclonal antibody, an RT-PCR analysis showed that the AB1 line expressed the mRNA encoding IFN-gamma, 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-2(181-188) 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 V-beta 11(+) AB1 cells exert an antitumor activity against syngeneic B16 melanoma through recognition of TRP-2(181-188) peptide in an H-2K(b)-restricted manner.
引用
收藏
页码:198 / 204
页数:7
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