Arthritis Care Res (Hoboken). 2014 Jun;66(6):949-55. doi: 10.1002/acr.22248.
The myeloid-related proteins 8 and 14 (MRP-8/MRP-14) and neutrophil-derived S100A12 are biomarkers of inflammation. They can be used to determine the relapse risk in patients with juvenile idiopathic arthritis (JIA) after stopping antiinflammatory treatment. In this study, we tested the performance of different enzyme-linked immunosorbent assays (ELISAs) in order to validate systems available for routine use.
MRP-8/MRP-14 and S100A12 serum concentrations of 188 JIA patients in remission were analyzed. Commercially available test systems were compared to experimental ELISAs established in house. The ability of the assays to identify JIA patients at risk for relapse was analyzed.
For MRP-8/MRP-14, the PhiCal Calprotectin and Buhlmann MRP8/14 Calprotectin ELISAs revealed hazard ratios of 2.3 and 2.1, respectively. For S100A12, the CircuLex S100A12/EN-RAGE ELISA revealed a hazard ratio of 3.1. The commercial assays allowed a JIA relapse prediction that was at least comparable to the experimental ELISAs.
For the prediction of JIA relapse after stopping medication, the biomarkers MRP-8/MRP-14 and S100A12 can be determined by using assays that are available for routine use. The tested commercial MRP-8/MRP-14 and S100A12 ELISAs showed a performance comparable to well-established experimental ELISA protocols when assay-specific cutoffs for the indication of relapse prediction are thoroughly applied.
髓系相关蛋白 8 和 14(MRP-8/MRP-14)和中性粒细胞衍生的 S100A12 是炎症的生物标志物。它们可用于确定接受抗炎治疗的幼年特发性关节炎(JIA)患者停药后的复发风险。在这项研究中,我们测试了不同酶联免疫吸附测定(ELISA)的性能,以验证可用于常规使用的系统。
分析了 188 名处于缓解期的 JIA 患者的 MRP-8/MRP-14 和 S100A12 血清浓度。比较了市售的测试系统和内部建立的实验 ELISA。分析了测定法识别有复发风险的 JIA 患者的能力。
对于 MRP-8/MRP-14,PhiCal Calprotectin 和 Buhlmann MRP8/14 Calprotectin ELISA 分别显示出 2.3 和 2.1 的风险比。对于 S100A12,CircuLex S100A12/EN-RAGE ELISA 显示出 3.1 的风险比。商业检测可用于预测 JIA 复发,其预测结果至少与实验 ELISA 相当。
对于停止用药后 JIA 复发的预测,可以使用市售的用于常规使用的检测方法来确定生物标志物 MRP-8/MRP-14 和 S100A12。在应用特定于检测的复发预测指标时,所测试的商业 MRP-8/MRP-14 和 S100A12 ELISA 显示出与成熟的实验 ELISA 方案相当的性能。