Dejaco Christian, Oppl Bastian, Monach Paul, Cuthbertson David, Carette Simon, Hoffman Gary, Khalidi Nader, Koening Curry, Langford Carol, McKinnon-Maksimowicz Kathleen, Seo Philip, Specks Ulrich, Ytterberg Steven, Merkel Peter A, Zwerina Jochen
Department of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.
1st Medical Department and Ludwig Boltzmann Institute of Osteology, Hanusch Hospital, Vienna, Austria.
PLoS One. 2015 Mar 26;10(3):e0121737. doi: 10.1371/journal.pone.0121737. eCollection 2015.
Previous studies suggest a role for eotaxin-3, TARC/CCL17 and IgG4 in newly-diagnosed patients with eosinophilic granulomatosis with polyangiitis (EGPA, Churg-Strauss) with highly active disease. The role of these biomarkers in relapsing disease is unclear.
Serum levels of TARC/CCL17, eotaxin-3, IgG4, and IgG4/IgG ratio were determined in serum samples from a longitudinal cohort of patients with EGPA (105 visits of 25 patients). Epidemiological, clinical and laboratory data were available for all visits.
At the first visit, 80% of patients were using glucocorticoids and 68% additional immunosuppressive drugs. Disease flares were seen at 18 visits. The median BVAS and BVAS/WG scores at time of relapse were 4 and 2, respectively. None of the biomarkers tested were useful to discriminate between active disease and remission. Patients treated with prednisone had lower eotaxin-3 and eosinophil levels compared to patients not taking glucocorticoids irrespective of disease activity. Use of immunosuppressive agents was not associated with biomarker levels.
Serum levels of TARC/CCL17, eotaxin-3, IgG4, and IgG4/IgG ratio do not clearly differentiate active and inactive disease in established EGPA. Defining biomarkers in EGPA remains a challenge especially during times of glucocorticoid use.
先前的研究表明,嗜酸性粒细胞趋化因子-3、胸腺和活化调节趋化因子/TARC/CCL17及IgG4在新诊断的高活动度嗜酸性肉芽肿性多血管炎(EGPA,Churg-Strauss综合征)患者中发挥作用。这些生物标志物在疾病复发中的作用尚不清楚。
测定了EGPA患者纵向队列血清样本中TARC/CCL17、嗜酸性粒细胞趋化因子-3、IgG4及IgG4/IgG比值(25例患者共105次就诊)。所有就诊的流行病学、临床和实验室数据均可得。
首次就诊时,80%的患者正在使用糖皮质激素,68%的患者还使用了其他免疫抑制剂。在18次就诊时出现疾病复发。复发时BVAS和BVAS/WG评分中位数分别为4分和2分。所检测的生物标志物均无助于区分疾病活动期和缓解期。无论疾病活动状态如何,与未服用糖皮质激素的患者相比,接受泼尼松治疗的患者嗜酸性粒细胞趋化因子-3和嗜酸性粒细胞水平较低。免疫抑制剂的使用与生物标志物水平无关。
在确诊的EGPA中,TARC/CCL17、嗜酸性粒细胞趋化因子-3、IgG4及IgG4/IgG比值的血清水平并不能明确区分疾病的活动期和非活动期。在EGPA中定义生物标志物仍然是一项挑战,尤其是在使用糖皮质激素期间。