Linker-Israeli M, Bakke A C, Kitridou R C, Gendler S, Gillis S, Horwitz D A
J Immunol. 1983 Jun;130(6):2651-5.
The objective of this study was to define some causes of the immunologic impairment characteristic of systemic lupus erythematosus. Blood mononuclear cells from 19 patients were stimulated to produce interleukin 1 and interleukin 2 and compared with controls. A severe defect in both IL 1 and IL 2 activity was observed. The low cytokine levels did not correlate with clinical or serologic activity of disease. These defects could not be explained by concurrent corticosteroid therapy. There was no correlation between a lower number of OKT4+ cells observed in these patients and the levels of IL 2 production, nor did removal of monocytes bring IL 2 to normal. Impaired IL 2 production could not be restored to normal by IL 1. The observed deficiency in these regulatory cytokines may therefore be a primary defect that is important in the pathogenesis of this disorder.
本研究的目的是明确系统性红斑狼疮免疫损伤特征的一些病因。对19例患者的血液单核细胞进行刺激以产生白细胞介素1和白细胞介素2,并与对照组进行比较。观察到白细胞介素1和白细胞介素2活性均存在严重缺陷。细胞因子水平较低与疾病的临床或血清学活性无关。这些缺陷无法用同时进行的皮质类固醇治疗来解释。在这些患者中观察到的OKT4 +细胞数量减少与白细胞介素2的产生水平之间没有相关性,去除单核细胞也不能使白细胞介素2恢复正常。白细胞介素1不能将受损的白细胞介素2产生恢复至正常水平。因此,观察到的这些调节性细胞因子缺乏可能是一种原发性缺陷,在该疾病的发病机制中起重要作用。