Penning C A, Wright J K, Ashby J C, Cunningham J, Rowell N R, Hughes P
J Clin Lab Immunol. 1983 Oct;12(2):77-81.
Sera from 7 of 37 patients with systemic sclerosis (SS) were found to markedly enhance cytotoxicity in several established human target cell lines when co-cultured with normal human peripheral blood mononuclear cells (PBM). Fractionation studies indicated that the cytotoxicity-inducing activity resided in the IgG-containing fractions of serum and that the effector cells were Fc-receptor positive. By contrast, sera from 27 normal controls produced little or no cytotoxicity when co-cultured with the same target cell lines and normal PBM. Any slight enhancement of cytotoxicity that occurred with a single target cell line was, on fractionation, either labile or associated with albumin containing fractions. These findings raise the possibility that antibody-dependent cellular cytotoxicity (ADCC) could provide a pathogenetic mechanism in some patients with SS.
在37例系统性硬化症(SS)患者中,发现7例患者的血清在与正常人外周血单个核细胞(PBM)共培养时,能显著增强几种已建立的人靶细胞系的细胞毒性。分级分离研究表明,细胞毒性诱导活性存在于血清中含IgG的组分中,效应细胞为Fc受体阳性。相比之下,27例正常对照的血清在与相同靶细胞系和正常PBM共培养时,产生的细胞毒性很小或没有。对于单个靶细胞系出现的任何轻微细胞毒性增强,经分级分离后,要么不稳定,要么与含白蛋白的组分有关。这些发现增加了抗体依赖性细胞毒性(ADCC)可能为某些SS患者提供发病机制的可能性。