Muratori P, Muratori L, Cassani F, Terlizzi P, Lenzi M, Rodrigo L, Bianchi F B
Department of Internal Medicine, Cardioangiology, Hepatology, Alma Mater Studiorum-University of Bologna, Bologna, Italy.
Clin Exp Immunol. 2002 Jan;127(1):172-5. doi: 10.1046/j.1365-2249.2002.01719.x.
Multiple nuclear dots pattern has been described in primary biliary cirrhosis and, less often, in rheumatological disorders. Sp100 is the major antigen of multiple nuclear dots. We evaluated prevalence and diagnostic significance of multiple nuclear dots and anti-Sp100 reactivity both in hepatic and rheumatological diseases. A series of 283 consecutive liver patients (89 primary biliary cirrhosis, 12 primary sclerosing cholangitis, 85 autoimmune hepatitis, 97 hepatitis C virus-related chronic liver disease) and of 89 consecutive rheumatological cases were evaluated. Presence of multiple nuclear dots was assessed by indirect immunofluorescence on HEp-2 cells, anti-Sp100 reactivity by ELISA with recombinant protein. Multiple nuclear dots were detected in 20 patients (7%) with liver disease (of whom 15 with primary biliary cirrhosis), and in eight patients (9%) with rheumatological disorders. Anti-Sp100 was detected in 45 liver patients (16%), of whom 30 with primary biliary cirrhosis, but in only two with rheumatological disorders (2%) (P =0.0004). The concordance between multiple nuclear dots and anti-Sp100 in liver and rheumatological patients was 90% and 25% (P=0.0018), respectively. Among 89 consecutive patients with primary biliary cirrhosis, multiple nuclear dots and anti-Sp100 were present in 17% and 34%, respectively (P=0.0152). Anti-Sp100 positivity was associated with older age and higher gamma-globulin levels. Multiple nuclear dots are similarly observed in liver and rheumatological patients. In contrast, anti-Sp100 is more frequent in liver patients and is significantly more often detected in primary biliary cirrhosis, of which it can be regarded as a highly specific serological marker. The antigenic target of multiple nuclear dots in most rheumatological patients is other than Sp100.
多核点模式已在原发性胆汁性肝硬化中被描述,在风湿性疾病中较少见。Sp100是多核点的主要抗原。我们评估了多核点和抗Sp100反应性在肝脏疾病和风湿性疾病中的患病率及诊断意义。对连续的283例肝病患者(89例原发性胆汁性肝硬化、12例原发性硬化性胆管炎、85例自身免疫性肝炎、97例丙型肝炎病毒相关慢性肝病)和89例连续的风湿性疾病病例进行了评估。通过在HEp-2细胞上进行间接免疫荧光评估多核点的存在,通过使用重组蛋白的ELISA评估抗Sp100反应性。在20例(7%)肝病患者(其中15例为原发性胆汁性肝硬化)和8例(9%)风湿性疾病患者中检测到多核点。在45例(16%)肝病患者中检测到抗Sp100,其中30例为原发性胆汁性肝硬化,但在风湿性疾病患者中仅2例(2%)检测到(P = 0.0004)。肝病和风湿性疾病患者中多核点与抗Sp100之间的一致性分别为90%和25%(P = 0.0018)。在连续的89例原发性胆汁性肝硬化患者中,多核点和抗Sp100的存在率分别为17%和34%(P = 0.0152)。抗Sp100阳性与年龄较大和γ-球蛋白水平较高相关。在肝病和风湿性疾病患者中均类似地观察到多核点。相比之下,抗Sp100在肝病患者中更常见,在原发性胆汁性肝硬化中显著更常检测到,可将其视为一种高度特异性的血清学标志物。大多数风湿性疾病患者中多核点的抗原靶点不是Sp100。