Wright J K, Penning C A, Ashby J C, Cunningham J, Rowell N R, Hughes P
J Clin Lab Immunol. 1983 Jun;11(2):81-5.
Sera from 6 out of 18 patients with systemic lupus erythematosus (SLE) were found to be capable of producing marked increases of 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 IgG containing fractions and that the effector cells were Fc-receptor positive. By contrast, sera from 27 normal controls produced little or no cytotoxicity when similarly co-cultured with the same target cell lines and normal PBM. Any slight reactivity that occasionally occurred against a single cell line was, on serum fractionation, either labile or associated with albumen containing fractions. These findings raise the possibility that antibody-dependent cellular cytotoxicity could provide an additional pathogenetic mechanism in patients with SLE.
在系统性红斑狼疮(SLE)患者中,18例中有6例患者的血清在与正常人外周血单个核细胞(PBM)共同培养时,被发现能够在几种已建立的人类靶细胞系中显著增强细胞毒性。分级分离研究表明,细胞毒性诱导活性存在于含IgG的组分中,效应细胞为Fc受体阳性。相比之下,27名正常对照者的血清在与相同的靶细胞系和正常PBM进行类似的共同培养时,几乎没有产生细胞毒性或根本没有细胞毒性。偶尔对单个细胞系出现的任何轻微反应,经血清分级分离后,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可能为SLE患者提供额外发病机制的可能性。