Wright J K, Hughes P, Rowell N R, Sneddon I B
Clin Exp Immunol. 1979 Apr;36(1):175-82.
Cell-mediated cytotoxicity was examined in thirty-seven patients with systemic sclerosis using both whole blood and purified peripheral blood mononuclear cells (PBM) to measure antibody-dependent (ADCC) and phytohaemagglutinin (PHA) induced lymphocyte cytotoxicity to 51Cr-labelled Chang liver cells. In twenty-three mildly affected patients, ADCC and PHA-induced cytotoxicity did not differ from that found in control populations. By contrast, fourteen patients severely affected by extensive visceral disease showed reductions in both ADCC and PHA-induced cytotoxicity which were more marked in whole blood assays (P less than 0.001) than in those performed with PBM (P less than 0.05). The addition of patient's sera to control cytotoxicity assays suggested that blocking or suppressive serum factors could only account for some of the disproportionate reduction in whole blood cytotoxicity which, in the main, must be due to a lack of circulating effector cells. These results are in agreement with previous findings of reduced numbers of circulating thymus-dependent lymphocytes in patients with severe disease, a defect of cell-mediated immunity that may result from the chronic antigenic stimulation of an autoimmune disease process.
采用全血和纯化的外周血单个核细胞(PBM)检测了37例系统性硬化症患者的细胞介导细胞毒性,以测定抗体依赖性(ADCC)和植物血凝素(PHA)诱导的淋巴细胞对51Cr标记的Chang肝细胞的细胞毒性。在23例轻度受累患者中,ADCC和PHA诱导的细胞毒性与对照组人群无差异。相比之下,14例受广泛内脏疾病严重影响的患者显示ADCC和PHA诱导的细胞毒性均降低,全血检测中的降低更为明显(P<0.001),而PBM检测中的降低则较轻(P<0.05)。将患者血清添加到对照细胞毒性检测中表明,阻断或抑制性血清因子只能解释全血细胞毒性不成比例降低的部分原因,主要原因一定是循环效应细胞的缺乏。这些结果与先前在重症患者中循环胸腺依赖性淋巴细胞数量减少的发现一致,这种细胞介导免疫缺陷可能是自身免疫疾病过程中慢性抗原刺激的结果。