Lassoued K, Guilly M N, Danon F, Andre C, Dhumeaux D, Clauvel J P, Brouet J C, Seligmann M, Courvalin J C
Laboratory of Immunochemistry and Immunopathology, INSERM U 108, University of Paris VII, France.
Ann Intern Med. 1988 Jun;108(6):829-33. doi: 10.7326/0003-4819-108-6-829.
In 11 patients, sera displaying a ringlike nuclear immunofluorescent staining on sections of rat liver tissue were shown by Western blotting to contain antibodies to lamins. Sera from 8 patients contained autoantibodies reacting with lamin B, whereas sera from the other 3 patients reacted with lamins A and C. All patients (9 women and 2 men) had a chronic autoimmune disorder, which rarely fulfilled the usual criteria for a diagnosis of systemic lupus erythematosus. The disorder was characterized by acute or chronic (active or granulomatous) hepatitis; steroid-responsive blood cytopenia, often associated with a circulating anticoagulant, or anticardiolipin antibodies, or both; and cutaneous leukocytoclastic angiitis or probable brain vasculitis. Eight patients had at least two of these three conditions. Antilamin autoantibodies may thus be a marker for an unusual subset of autoimmune diseases.
在11例患者中,通过蛋白质印迹法显示,在大鼠肝组织切片上呈现环状核免疫荧光染色的血清含有抗核纤层蛋白抗体。8例患者的血清含有与核纤层蛋白B反应的自身抗体,而另外3例患者的血清与核纤层蛋白A和C发生反应。所有患者(9名女性和2名男性)均患有慢性自身免疫性疾病,很少符合系统性红斑狼疮的常规诊断标准。该疾病的特征为急性或慢性(活动性或肉芽肿性)肝炎;类固醇反应性血细胞减少症,常伴有循环抗凝物质或抗心磷脂抗体,或两者兼有;以及皮肤白细胞破碎性血管炎或可能的脑血管炎。8例患者至少具备这三种情况中的两种。因此,抗核纤层蛋白自身抗体可能是自身免疫性疾病一个不寻常亚群的标志物。