Dong X, Wang J, Kabir F N, Shaw M, Reed A M, Stein L, Andrade L E, Trevisani V F, Miller M L, Fujii T, Akizuki M, Pachman L M, Satoh M, Reeves W H
Thurston Arthritis Research Center and Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, USA.
Arthritis Rheum. 2000 Jan;43(1):85-93. doi: 10.1002/1529-0131(200001)43:1<85::AID-ANR11>3.0.CO;2-D.
To evaluate the specificity of anti-DEK antibodies for juvenile rheumatoid arthritis (JRA).
Anti-DEK autoantibodies were measured by enzyme-linked immunosorbent assay (ELISA) using affinity-purified his6-DEK fusion protein. Sera from 639 subjects (417 patients with systemic autoimmune disease, 13 with sarcoidosis, 44 with pulmonary tuberculosis, 125 with uveitis, and 6 with scleritis, and 34 healthy control subjects) were screened. Reactivity was verified by immunoblotting and immunoprecipitation studies using baculovirus-expressed human DEK.
Anti-DEK activity was found at the following frequencies: JRA 39.4% (n = 71), systemic lupus erythematosus (SLE) 25.1% (n = 216), sarcoidosis 46.2% (n = 13), rheumatoid arthritis 15.5% (n = 71), systemic sclerosis 36.0% (n = 22), polymyositis 6.2% (n = 16), and adult Still's disease 0% (n = 21). Autoantibodies also were detected in 9.1% of tuberculosis sera (n = 44), but were undetectable in sera from the 34 healthy controls. Western blot and immunoprecipitation assay results correlated well with the ELISA findings. In general, levels of anti-DEK autoantibodies were higher in SLE than in other patient subsets, including JRA.
Anti-DEK autoantibodies are less specific for JRA than previously believed. They are produced in association with a variety of inflammatory conditions, many of which are associated with granuloma formation and/or predominant Thl cytokine production. Anti-DEK antibodies may be a marker for a subset of autoimmunity associated with interferon-gamma production rather than a particular disease subset.
评估抗DEK抗体对青少年类风湿性关节炎(JRA)的特异性。
使用亲和纯化的his6-DEK融合蛋白,通过酶联免疫吸附测定(ELISA)检测抗DEK自身抗体。对639名受试者(417名系统性自身免疫性疾病患者、13名结节病患者、44名肺结核患者、125名葡萄膜炎患者、6名巩膜炎患者以及34名健康对照者)的血清进行筛查。通过使用杆状病毒表达的人DEK进行免疫印迹和免疫沉淀研究来验证反应性。
抗DEK活性出现的频率如下:JRA为39.4%(n = 71),系统性红斑狼疮(SLE)为25.1%(n = 216),结节病为46.2%(n = 13),类风湿性关节炎为15.5%(n = 71),系统性硬化症为36.0%(n = 22),多发性肌炎为6.2%(n = 16),成人斯蒂尔病为0%(n = 21)。在9.1%的肺结核血清(n = 44)中也检测到自身抗体,但在34名健康对照者的血清中未检测到。蛋白质印迹和免疫沉淀试验结果与ELISA结果高度相关。总体而言,SLE中抗DEK自身抗体水平高于包括JRA在内的其他患者亚组。
抗DEK自身抗体对JRA的特异性低于先前认为的程度。它们与多种炎症性疾病相关产生,其中许多与肉芽肿形成和/或主要的Th1细胞因子产生有关。抗DEK抗体可能是与干扰素-γ产生相关的自身免疫亚组的标志物,而非特定疾病亚组的标志物。