Harada M, Tamada K, Abe K, Li T, Onoe Y, Tada H, Tatsugami K, Ando T, Kimura G, Nomoto K
Department of Virology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Cancer Immunol Immunother. 1998 Dec;47(4):198-204. doi: 10.1007/s002620050521.
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 Vbeta11. 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)-gamma 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-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 Vbeta11+ AB1 cells exert an antitumor activity against syngeneic B16 melanoma through recognition of TRP-2(181-188) peptide in an H-2Kb-restricted manner.
从经白细胞介素(IL)-12治疗治愈B16黑色素瘤的C57BL/6小鼠的脾细胞中建立了一种B16黑色素瘤特异性CD8 + T细胞系(AB1)。AB1系专门使用T细胞受体Vbeta11。AB1细胞对同基因B16黑色素瘤和异基因P815肥大细胞瘤均表现出细胞溶解活性,而冷抑制试验揭示了AB1细胞对B16黑色素瘤的特异性。通过转染H-2Kb基因恢复了它们杀死B16黑色素瘤I类缺失变体的能力。此外,添加抗H-2Kb单克隆抗体可显著抑制它们的干扰素(IFN)-γ产生,RT-PCR分析表明AB1系表达编码IFN-γ的mRNA,但不表达IL-4或IL-10。使用酪氨酸酶相关蛋白2(TRP-2)合成肽的实验表明,AB1细胞可以识别TRP-2(181 - 188)肽。此外,AB1细胞对已建立的B16黑色素瘤肺转移显示出体内抗肿瘤作用。总体而言,这些结果表明,Tc1型Vbeta11 + AB1细胞通过以H-2Kb限制的方式识别TRP-2(181 - 188)肽,对同基因B16黑色素瘤发挥抗肿瘤活性。