Pignata C, Vajro P, Monaco G, Fontanella A
J Pediatr Gastroenterol Nutr. 1986 Jul-Aug;5(4):537-41. doi: 10.1097/00005176-198607000-00005.
Suppressor cell function was evaluated in children affected by HBsAg-positive chronic active hepatitis. Circulating concanavalin A- (ConA) precultured lymphocytes failed to suppress the proliferative response of autologous responder cells to a mitogen. In four of eight patients with a failure of ConA-induced suppressor activity, indomethacin added during the induction phase of T suppressor cells abolished the defect, indicating that prostaglandin-producing adherent cells may influence ConA-induced suppressor activity. An inverse relationship between suppressor cell activity and the number of suppressor/cytotoxic subsets defined by the OK T8 monoclonal antibody was found. Our findings strongly support the hypothesis that an abnormality in the immunoregulatory system plays a role in the pathogenesis of HBsAg-related chronic active hepatitis. It is also suggested that non-T regulatory cells are implicated in the immunological abnormality in chronic active hepatitis.
对受乙肝表面抗原阳性慢性活动性肝炎影响的儿童的抑制细胞功能进行了评估。循环中的伴刀豆球蛋白A(ConA)预培养淋巴细胞未能抑制自体反应细胞对有丝分裂原的增殖反应。在8例ConA诱导的抑制活性失败的患者中,有4例在T抑制细胞诱导期添加消炎痛后消除了缺陷,这表明产生前列腺素的黏附细胞可能影响ConA诱导的抑制活性。发现抑制细胞活性与由OK T8单克隆抗体定义的抑制/细胞毒性亚群数量之间呈负相关。我们的研究结果有力地支持了免疫调节系统异常在乙肝表面抗原相关慢性活动性肝炎发病机制中起作用的假说。还提示非T调节细胞与慢性活动性肝炎的免疫异常有关。