van Venrooij W J, Wodzig K W, Habets W J, de Rooij D J, van de Putte L B
Department of Biochemistry, University of Nijmegen, The Netherlands.
Clin Exp Rheumatol. 1989 May-Jun;7(3):277-82.
A novel frequently occurring autoantibody specificity in serum from connective tissue disease patients is described. The autoantibodies as detected by immunoblotting are directed against a 56,000 Dalton (56K) antigen, that after biochemical fractionation predominantly is found in the cytoplasmic fraction of various cell types and tissues. Attempts to localize the antigen more precisely were unsuccessful primarily because these antibodies do not produce a positive immunofluorescence pattern. The antigen in its native form is not associated with DNA or one of the common cytoplasmic or nuclear RNAs in the cell. Immunoprecipitation studies also showed that the protein is not closely associated with other proteins in a multi-component complex. Anti-56K antibodies are found in about 8% of patients with connective tissue disease, most commonly in patients with Sjögren's syndrome (14%). It is not found in patients with mixed connective tissue disease, polymyositis/dermatomyositis or scleroderma and rarely (less than 1%) in healthy control subjects. The fact that 22% of the anti-56K sera also contain La/SS-B antibodies support the idea that this antibody specificity might be characteristic for a subclass of Sjögren's syndrome patients.
本文描述了结缔组织病患者血清中一种新的常见自身抗体特异性。通过免疫印迹检测到的自身抗体针对一种56,000道尔顿(56K)的抗原,该抗原在生化分级分离后主要存在于各种细胞类型和组织的细胞质部分。更精确地定位该抗原的尝试未成功,主要原因是这些抗体未产生阳性免疫荧光模式。天然形式的抗原与细胞中的DNA或常见的细胞质或核RNA之一无关。免疫沉淀研究还表明,该蛋白在多组分复合物中与其他蛋白没有紧密关联。约8%的结缔组织病患者体内可检测到抗56K抗体,最常见于干燥综合征患者(14%)。混合性结缔组织病、多发性肌炎/皮肌炎或硬皮病患者体内未发现该抗体,健康对照者中也很少见(不到1%)。22%的抗56K血清中还含有La/SS - B抗体,这一事实支持了这种抗体特异性可能是干燥综合征患者亚类特征的观点。