Dosch H M, Gelfand E W
J Immunol. 1978 Nov;121(5):2097-105.
The addition of fresh peripheral blood mononuclear cells (PBL) from four of seven patients with agammaglobulinemia to generated hemolytic plaque-forming cells (PFC) resulted in a dose-dependent suppression of PFC. This spontaneous suppressor cell activity (SSA) was restricted to the four patients who could generate a PFC response in vitro. SSA was mediated by a small subset of E-rosetting T lymphocytes characterized by theophylline-sensitive E-receptors and surface receptors for Fc-IgG. The effects of SSA were temperature dependent and reversible, and pokeweed mitogen could prevent the rapid decline of SSA observed during culture. Augmentation of SSA was achieved by agents known to increase intracellular levels of cyclic AMP, whereas lithium chloride abrogated SSA, including the drug-induced effects. Cells mediating SSA may play a role in preventing the normal transition of pre-B cells to B cells in patients with agammaglobulinemia without B lymphocytes.
将7例无丙种球蛋白血症患者中4例的新鲜外周血单个核细胞(PBL)加入到生成的溶血空斑形成细胞(PFC)中,导致PFC呈剂量依赖性抑制。这种自发抑制细胞活性(SSA)仅限于4例能够在体外产生PFC反应的患者。SSA由一小部分E花环形成T淋巴细胞介导,其特征为对茶碱敏感的E受体和Fc-IgG表面受体。SSA的作用是温度依赖性且可逆的,商陆有丝分裂原可防止培养过程中观察到的SSA快速下降。已知增加细胞内环磷酸腺苷水平的药物可增强SSA,而氯化锂可消除SSA,包括药物诱导的效应。介导SSA的细胞可能在无B淋巴细胞的无丙种球蛋白血症患者中,阻止前B细胞向B细胞的正常转变中发挥作用。