Trent R J, Clancy R L, Danis V, Basten A
Clin Exp Immunol. 1981 Jul;45(1):9-17.
B co-culture system was used to test for the presence of disordered immune homeostasis in the autoimmune disease, chronic idiopathic thrombocytopenic purpura (ITP). Various numbers of T cells were added to a fixed number of B cells in the presence or absence of the polyclonal activator, pokeweed mitogen, and IgG production measured in the culture supernatants 6 days later. The results demonstrated a defect in T cell-dependent suppression and/or a state of B cell hyper-responsiveness in lymphocytes from patients compared to normal controls. The loss of T cell-dependent suppression could not be readily explained in terms of the therapy being used nor by the presence of circulating IgG containing immune complexes. The findings of a similar abnormality in some cases of non-immune thrombocytopenia suggested that the reduction in suppression observed in chronic ITP was unlikely to be a primary event in disease pathogenesis, although it could well contribute to the ongoing autoimmune response.
采用A T:B共培养系统来检测自身免疫性疾病慢性特发性血小板减少性紫癜(ITP)中免疫稳态紊乱的存在情况。在存在或不存在多克隆激活剂商陆有丝分裂原的情况下,将不同数量的T细胞添加到固定数量的B细胞中,并在6天后测量培养上清液中的IgG产量。结果表明,与正常对照相比,患者淋巴细胞中存在T细胞依赖性抑制缺陷和/或B细胞高反应性状态。T细胞依赖性抑制的丧失既不能通过所使用的治疗方法轻易解释,也不能通过含有循环免疫复合物的IgG的存在来解释。在一些非免疫性血小板减少症病例中发现了类似的异常情况,这表明在慢性ITP中观察到的抑制作用降低不太可能是疾病发病机制中的主要事件,尽管它很可能促成正在进行的自身免疫反应。