Kyriatsoulis A, Manns M, Gerken G, Lohse A W, Ballhausen W, Reske K, Meyer zum Büschenfelde K H
I. Medizinische Klinik und Poliklinik, Johannes Gutenberg-Universität Mainz, FRG.
Clin Exp Immunol. 1987 Oct;70(1):53-60.
Using one-dimensional and two-dimensional immunoblotting techniques the reactions of sera from 14 patients with liver-kidney microsomal (LKM) antibody positive chronic active hepatitis (CAH) with human liver microsomal preparations was compared with the reaction of sera from 12 healthy persons and from five patients with systemic lupus erythematosus (SLE). All sera displayed a multiplicity of reactions. This demonstrates the presence of many autoantibodies in normal human sera. It could be shown that all sera react with the cytoskeletal antigens cytokeratin, actin and actomyosin. These reactions were more marked in the autoimmune sera, i.e. LKM-positive CAH and SLE. Densitometric subtraction was found to be a reliable technique to distinguish the natural antigen/autoantibody reactions from pathological, disease-characteristic autoantibodies. It was shown that the pathological LKM autoantibodies recognize non species-specific microsomal proteins at 50 kD of pI 7.5-8.0 at high titres, which are only very weakly recognized by normal or SLE sera. We recommend sensitive immunoblotting techniques and densitometric subtraction as the currently most accurate method to distinguish natural from pathological autoantibodies.
运用一维和二维免疫印迹技术,将14例肝肾微粒体(LKM)抗体阳性的慢性活动性肝炎(CAH)患者血清与人肝微粒体制剂的反应,与12名健康人和5例系统性红斑狼疮(SLE)患者血清的反应进行了比较。所有血清均呈现多种反应。这表明正常人血清中存在多种自身抗体。结果显示,所有血清均与细胞骨架抗原细胞角蛋白、肌动蛋白和肌动球蛋白发生反应。这些反应在自身免疫性血清中更为明显,即LKM阳性的CAH和SLE血清。发现光密度减法是区分天然抗原/自身抗体反应与病理性、疾病特征性自身抗体的可靠技术。结果表明,病理性LKM自身抗体以高滴度识别pI 7.5 - 8.0、分子量50 kD的非种属特异性微粒体蛋白,而正常或SLE血清对这些蛋白的识别非常微弱。我们推荐灵敏的免疫印迹技术和光密度减法作为目前区分天然自身抗体与病理性自身抗体最准确的方法。