EISEN H N, KERN M, NEWTON W T, HELMREICH E
J Exp Med. 1959 Aug 1;110(2):187-206. doi: 10.1084/jem.110.2.187.
Although induction of contact skin sensitivity by low molecular weight 2,4-dinitrobenzenes requires the formation in vivo of 2,4-dinitrophenyl-proteins, analogous protein conjugates prepared in vitro are unable to induce this hypersensitive state. Low molecular weight 2,4-dinitrobenzenes are concentrated by isolated lymph node cells, but a representative 2,4-dinitrophenyl-protein conjugate (2,4-dinitrophenyl-bovine serum albumin) was not taken up to a detectable extent by these cells. It is inferred that there exist large quantitative differences in the extent to which dinitrophenyl-proteins are localized within cells following the administration to an intact animal of (a) those simple dinitrobenzenes which are both concentrated by lymph node cells and have the capacity to form protein conjugates in vivo, and (b) 2,4-dinitrophenyl-protein conjugates prepared in vitro. It is suggested that this difference could account for the fact that a varietyof 2,4-dinitrophenyl-proteins prepared in vitro are unable to induce contact skin sensitivity.
尽管低分子量的2,4 -二硝基苯诱导接触性皮肤敏感性需要在体内形成2,4 -二硝基苯基蛋白质,但体外制备的类似蛋白质共轭物却无法诱导这种超敏状态。低分子量的2,4 -二硝基苯被分离的淋巴结细胞浓缩,但一种代表性的2,4 -二硝基苯基蛋白质共轭物(2,4 -二硝基苯基 - 牛血清白蛋白)未被这些细胞摄取到可检测的程度。据推断,在向完整动物施用以下两种物质后,二硝基苯基蛋白质在细胞内定位的程度存在很大的数量差异:(a) 那些既被淋巴结细胞浓缩又有能力在体内形成蛋白质共轭物的简单二硝基苯,以及(b) 体外制备的2,4 -二硝基苯基蛋白质共轭物。有人认为,这种差异可以解释体外制备的多种2,4 -二硝基苯基蛋白质无法诱导接触性皮肤敏感性这一事实。