de Galocsy C, Jenkins P J, Mieli-Vergani G, Eddleston A L, Williams R
Clin Exp Immunol. 1981 Mar;43(3):486-90.
Suppressor T cell activity was studied serially in 11 patients with HBsAg-negative chronic active hepatitis when the disease was clinically and histologically inactive and during relapse using a short-lived suppressor cell assay. With a concentration of concanavalin A which gave a suboptimal proliferative response in normal subjects, the expected increase in thymidine incorporation was seen when the addition of the mitogen was delayed for 24 hr after the start of the lymphocyte culture period, a finding consistent with the disappearance of functional suppressor cells during the initial incubation. This effect was seen both in normal subjects and in patients with inactive disease, but was not observed at times of relapse. Further studies revealed a marked increase in lymphocyte sensitivity to concanavalin A at these times, a finding which might explain the apparent decrease in suppressor cell activity. When lower concentrations of mitogen were used in the assay, however, a significant reduction in suppressor cell activity was observed in the patients with chronic active hepatitis which was almost equal in magnitude in both the active and inactive groups, suggesting the presence of a true suppressor cell defect in this disease.
采用短期抑制细胞检测法,对11例HBsAg阴性慢性活动性肝炎患者在疾病临床和组织学静止期以及复发期进行了系列抑制性T细胞活性研究。在正常受试者中使用能产生次优增殖反应的刀豆蛋白A浓度,当淋巴细胞培养期开始24小时后延迟添加促有丝分裂原时,观察到胸苷掺入预期增加,这一发现与初始孵育期间功能性抑制细胞的消失一致。在正常受试者和疾病静止期患者中均观察到这种效应,但在复发期未观察到。进一步研究显示,此时淋巴细胞对刀豆蛋白A的敏感性显著增加,这一发现可能解释了抑制细胞活性的明显降低。然而,当检测中使用较低浓度的促有丝分裂原时,慢性活动性肝炎患者的抑制细胞活性显著降低,在活动组和静止组中降低幅度几乎相同,提示该疾病存在真正的抑制细胞缺陷。