Sy M S, Bach B A, Brown A, Nisonoff A, Benacerraf B, Greene M I
J Exp Med. 1979 Nov 1;150(5):1229-40. doi: 10.1084/jem.150.5.1229.
Anti-p-azobenzenearsonate (ABA) antibodies, coupled covalently to normal syngeneic spleen cells and then given intravenously to normal animals, were found to be potent tolerogens for delayed-type hypersensitivity (DTH) to ABA. The ability of the antibody-coupled cells to induce tolerance was determined to be a result of the cross-reactive idiotype (CRI+) fraction of the antibodies, because anti-ABA antibodies lacking the CRI+ components when coupled to spleen cells were unable to cause any significant inhibition. Furthermore, genetic analysis revealed that the ability of CRI-coupled cells to inhibit ABA-specific DTH is linked to Igh-1 heavy chain allotype, in as much animals which possess heavy chain allotypes similar to that of A/J were sensitive to this inhibition. Adoptive transfer experiments provided evidence that CRI-coupled cells induce suppressor cells, and spleen cells or thymocytes from animals received CRI-coupled cells were able to transfer suppression to naive recipients. In addition, treatment with anti-Thy1.2 serum plus complement completely abrogated their ability to transfer suppression. Thus, this active suppression is a T-cell-dependent phenomenon. In investigating the specificity of these suppressor T cells, it was found that they functioned in an antigen-specific manner and were unable to suppress the development of DTH to an unrelated hapten 2,4-dinitro-1-fluorobenzene.
将抗对氨基苯砷酸盐(ABA)抗体与同基因正常脾细胞共价偶联,然后静脉注射给正常动物,发现其是诱导对ABA迟发型超敏反应(DTH)的有效耐受原。抗体偶联细胞诱导耐受的能力被确定是抗体的交叉反应独特型(CRI+)部分的结果,因为与脾细胞偶联时缺乏CRI+成分的抗ABA抗体不能引起任何显著抑制。此外,遗传分析表明,CRI偶联细胞抑制ABA特异性DTH的能力与Igh-1重链同种异型相关,因为具有与A/J相似重链同种异型的动物对这种抑制敏感。过继转移实验提供了证据,证明CRI偶联细胞诱导抑制细胞,接受CRI偶联细胞的动物的脾细胞或胸腺细胞能够将抑制作用转移给未接触过抗原的受体。此外,用抗Thy1.2血清加补体处理完全消除了它们转移抑制的能力。因此,这种主动抑制是一种T细胞依赖性现象。在研究这些抑制性T细胞的特异性时,发现它们以抗原特异性方式发挥作用,并且不能抑制对无关半抗原2,4-二硝基-1-氟苯的DTH反应的发展。