Holding Stephen, Fisher Victoria J, Abuzakouk Mohamed
Immunology Department, Hull Royal Infirmary, Hull, UK
Hull York Medical School, Hull, UK.
Ann Clin Biochem. 2015 Mar;52(Pt 2):297-301. doi: 10.1177/0004563214533668. Epub 2014 Apr 10.
Monitoring of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) in remission usually includes indirect immunofluorescence (IIF), proteinase 3 (PR3)-ANCA and myeloperoxidase (MPO)-ANCA. Typically, PR3 and MPO-ANCA are both performed because patients sometimes switch specificity during follow up. Published data are limited to case reports and incidence of change is not reported. The aim of this study was to quantify the incidence of antibody switching.
Hull and East Yorkshire Hospitals National Health Service Trust serves a population of 720,000 for ANCA testing. We reviewed all ANCA results from January 2000 to August 2012 to quantify incidence of antibody switching. A total of 22,002 IIF screens (14,518 patients) were performed. A total of 9838 (45%) also had PR3- and MPO-ANCA (6439, 44% of patients). Patients that changed specificity from PR3- to MPO-ANCA and vice versa were identified and case notes reviewed.
A total of 218 patients with confirmed AAV positive for PR3/MPO-ANCA were followed for a mean of 2.6 years (range <0.1 to 12.4 years; with 113 (52%) patients followed for >1 year). Five patients (2%) changed specificity during follow up (3 GPA, 1 MPA & 1 EGPA). In two patients this was associated with relapse. Incidence of specificity change was 1 per 82 years (including two reversions to presenting specificity) and one per 286 years for changes associated with relapse. Monitoring using only the initial antibody specificity would have resulted in missed relapse in one patient.
Antibody specificity changes in AAV are rare. Monitoring only the initial antibody specificity would have missed clinical events but rising C-reactive protein presaged relapse in these cases.
在缓解期监测抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)通常包括间接免疫荧光法(IIF)、蛋白酶3(PR3)-ANCA和髓过氧化物酶(MPO)-ANCA检测。通常会同时检测PR3和MPO-ANCA,因为患者在随访过程中有时会出现特异性改变。已发表的数据仅限于病例报告,且未报道改变的发生率。本研究的目的是量化抗体转换的发生率。
赫尔和东约克郡医院国民保健服务信托基金为72万人提供ANCA检测服务。我们回顾了2000年1月至2012年8月期间所有的ANCA检测结果,以量化抗体转换的发生率。共进行了22,002次IIF筛查(14,518例患者)。其中9838例(45%)还进行了PR3-和MPO-ANCA检测(6439例患者,占44%)。确定了从PR3-ANCA转换为MPO-ANCA以及反之亦然的患者,并查阅了病历。
共有218例确诊为AAV且PR3/MPO-ANCA阳性的患者接受了平均2.6年的随访(范围为<0.1至12.4年;113例(52%)患者随访时间>1年)。5例患者(2%)在随访期间出现特异性改变(3例肉芽肿性多血管炎(GPA),1例显微镜下多血管炎(MPA)和1例嗜酸性肉芽肿性多血管炎(EGPA))。其中2例患者的特异性改变与病情复发相关。特异性改变的发生率为每82年1例(包括2例恢复至初始特异性),与复发相关的改变发生率为每286年1例。仅根据初始抗体特异性进行监测会导致1例患者的复发被漏诊。
AAV中的抗体特异性改变很少见。仅监测初始抗体特异性会遗漏临床事件,但在这些病例中,C反应蛋白升高预示着病情复发。