Giacomini P, Aguzzi A, Ferrone S
Hybridoma. 1986 Winter;5(4):277-88. doi: 10.1089/hyb.1986.5.277.
Recombinant immune interferon (IFN-gamma) induced a dose-related increase in the synthesis and expression of HLA class II antigens by the cultured melanoma cells COLO 38. Although IFN-gamma-treated melanoma cells COLO 38 continue to express higher levels of HLA-DR antigens than of HLA-DQ antigens, the effect of IFN-gamma was more marked on HLA-DQ antigens than on HLA-DR antigens, as indicated by the dose and incubation time required to induce the changes and by the extent and duration of the increase. The effect of IFN-gamma on HLA class II antigens is significantly higher than that of leukocyte and fibroblast interferons. Analysis by one- and two-dimensional gel electrophoresis of antigens synthesized by melanoma cells COLO 38 in the presence of IFN-gamma did not detect any significant change in the structural profile of the subunits of HLA-DR and -DQ antigens.
重组免疫干扰素(IFN-γ)可诱导培养的黑色素瘤细胞COLO 38合成并表达HLA II类抗原,且呈剂量相关增加。尽管经IFN-γ处理的黑色素瘤细胞COLO 38持续表达的HLA-DR抗原水平高于HLA-DQ抗原,但IFN-γ对HLA-DQ抗原的作用比对HLA-DR抗原更为显著,这可通过诱导变化所需的剂量和孵育时间以及增加的程度和持续时间来表明。IFN-γ对HLA II类抗原的作用明显高于白细胞干扰素和成纤维细胞干扰素。对在IFN-γ存在下黑色素瘤细胞COLO 38合成的抗原进行一维和二维凝胶电泳分析,未检测到HLA-DR和-DQ抗原亚基的结构轮廓有任何显著变化。