Vincent C, de Keyser F, Masson-Bessière C, Sebbag M, Veys E M, Serre G
Department of Biology and Pathology of the Cell, INSERM CJF 96-02, IFR 30, Purpan Medical School, University of Toulouse III, France.
Ann Rheum Dis. 1999 Jan;58(1):42-8. doi: 10.1136/ard.58.1.42.
Antiperinuclear factor (APF), "antikeratin antibodies" ("AKA"), and antibodies to human epidermis filaggrin (AFA), are highly specific serological markers of rheumatoid arthritis (RA), which recognise epitopes on various isoforms of (pro)filaggrin. It was proposed that these antibodies are globally named antifilaggrin autoantibodies. Here the diagnostic value of the detection of each one is compared and the overlap between the three tests evaluated.
492 serum samples were tested, including 279 RA serum samples, taken from patients in France and Belgium. APF and "AKA" titres were estimated by indirect immunofluorescence, and AFA titres by immunoblotting on filaggrin enriched human epidermis extracts.
By a convenient choice of the positivity thresholds, the diagnostic sensitivity and specificity of the tests were shown to be similar (0.52 and 0.97, respectively). Although the antibody titres were strongly correlated, the associations APF-AFA or AFA-"AKA" permitted more than 52% or 55% of RA to be diagnosed, with a specificity of 0.99.
APF, "AKA", and AFA detection have a similar diagnostic value. However, because the three tests do not totally overlap, associating APF with "AKA" or AFA with "AKA" can improve diagnostic sensitivity. None of the three antigens used bear all the epitopes recognised by antifilaggrin autoantibodies.
抗核周因子(APF)、“抗角蛋白抗体”(“AKA”)和抗人表皮聚角蛋白微丝蛋白抗体(AFA)是类风湿关节炎(RA)高度特异的血清学标志物,它们识别(前)聚角蛋白微丝蛋白各种异构体上的表位。有人提议将这些抗体统称为抗聚角蛋白微丝蛋白自身抗体。本文比较了检测每种抗体的诊断价值,并评估了这三项检测之间的重叠情况。
检测了492份血清样本,其中包括取自法国和比利时患者的279份RA血清样本。通过间接免疫荧光法测定APF和“AKA”滴度,通过对富含聚角蛋白微丝蛋白的人表皮提取物进行免疫印迹法测定AFA滴度。
通过合理选择阳性阈值,显示这些检测的诊断敏感性和特异性相似(分别为0.52和0.97)。虽然抗体滴度高度相关,但APF与AFA或AFA与“AKA”的联合检测可诊断超过52%或55%的RA患者,特异性为0.99。
APF、“AKA”和AFA检测具有相似的诊断价值。然而,由于这三项检测并不完全重叠,将APF与“AKA”或AFA与“AKA”联合使用可提高诊断敏感性。所使用的三种抗原均未包含抗聚角蛋白微丝蛋白自身抗体识别的所有表位。