GELL P G, SILVERSTEIN A M
J Exp Med. 1962 May 1;115(5):1037-51. doi: 10.1084/jem.115.5.1037.
Further data have been presented showing that the specificity of the delayed hypersensitivity reaction in the guinea pig to hapten-protein conjugates involves to a considerable degree a contribution by the protein carrier. The carrier contribution is such that sensitization to guinea pig albumin-m-azobenzenesulfonate, for example, does not result in cross-reaction with conjugates of the same hapten with unrelated proteins such as ovalbumin or human gamma globulin, nor were cross-reactions observed between conjugates prepared with the same hapten, coupled to the same protein, but by two different chemical routes, such that the point of attachment of the hapten to the protein differed. It thus appears that in this system both hapten and carrier protein are necessary, but that neither alone is in general sufficient to stimulate the delayed sensitive cell. Desensitization experiments with cross-reacting hapten-protein conjugates have suggested the presence of a multiplicity of antigenic determinants participating in the elicitation of the delayed lesion, and of a concomitant development of a heterogeneity of specificities in the population of delayed sensitive cells in the sensitized animal. The data are discussed in terms of the apparent requirement of the delayed sensitivity mechanism for a larger functional antigenic determinant than that required for interaction with circulating antibodies. Some possible explanations for this difference, and some of its consequences, are discussed.
更多数据表明,豚鼠对半抗原 - 蛋白质结合物的迟发型超敏反应的特异性在很大程度上涉及蛋白质载体的作用。例如,载体的作用使得对豚鼠白蛋白 - 间 - 偶氮苯磺酸盐致敏不会导致与相同半抗原与无关蛋白质(如卵清蛋白或人γ球蛋白)的结合物发生交叉反应,在用相同半抗原与相同蛋白质偶联但通过两种不同化学途径制备的结合物之间也未观察到交叉反应,使得半抗原与蛋白质的连接点不同。因此,在这个系统中,半抗原和载体蛋白似乎都是必需的,但通常单独任何一个都不足以刺激迟发型敏感细胞。用交叉反应性半抗原 - 蛋白质结合物进行的脱敏实验表明,存在多种抗原决定簇参与迟发型损伤的引发,并且在致敏动物的迟发型敏感细胞群体中伴随着特异性异质性的发展。根据迟发型敏感机制对比与循环抗体相互作用所需的更大功能抗原决定簇的明显需求来讨论这些数据。讨论了这种差异的一些可能解释及其一些后果。