Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka, 589-8511, Japan.
Clinical Research Center, Kindai University Hospital, Osaka-Sayama, Osaka, Japan.
Sci Rep. 2020 Sep 16;10(1):14879. doi: 10.1038/s41598-020-71848-4.
IgG4-related disease (IgG4-RD) is a multi-organ autoimmune disease characterized by elevated serum IgG4 concentration. Although serum IgG4 concentration is widely used as a biomarker for IgG4-RD and type 1 autoimmune pancreatitis (AIP), a pancreatic manifestation of IgG4-RD, a significant number of patients have normal serum IgG4 levels, even in the active phase of the disease. Recently, we reported that the development of experimental AIP and human type 1 AIP is associated with increased expression of IFN-α and IL-33 in the pancreas. In this study, we assessed the utility of serum IFN-α and IL-33 levels as biomarkers for type 1 AIP and IgG4-RD. Serum IFN-α and IL-33 concentrations in patients who met the diagnostic criteria for definite type 1 AIP and/or IgG4-RD were significantly higher than in those with chronic pancreatitis or in healthy controls. Strong correlations between serum IFN-α, IL-33, and IgG4 concentrations were observed. Diagnostic performance of serum IFN-α and IL-33 concentrations as markers of type 1 AIP and/or IgG4-RD was comparable to that of serum IgG4 concentration, as calculated by the receiver operating characteristic curve analysis. Induction of remission by prednisolone treatment markedly decreased the serum concentration of these cytokines. We conclude that serum IFN-α and IL-33 concentrations can be useful as biomarkers for type 1 AIP and IgG4-RD.
IgG4 相关疾病(IgG4-RD)是一种多器官自身免疫性疾病,其特征是血清 IgG4 浓度升高。虽然血清 IgG4 浓度被广泛用作 IgG4-RD 和 1 型自身免疫性胰腺炎(AIP)的生物标志物,AIP 是 IgG4-RD 的胰腺表现,但相当数量的患者的血清 IgG4 水平正常,即使在疾病的活动期也是如此。最近,我们报道了实验性 AIP 和人类 1 型 AIP 的发展与胰腺中 IFN-α和 IL-33 的表达增加有关。在这项研究中,我们评估了血清 IFN-α和 IL-33 水平作为 1 型 AIP 和 IgG4-RD 生物标志物的效用。符合明确 1 型 AIP 和/或 IgG4-RD 诊断标准的患者的血清 IFN-α和 IL-33 浓度明显高于慢性胰腺炎患者或健康对照者。血清 IFN-α、IL-33 和 IgG4 浓度之间存在强烈相关性。通过受试者工作特征曲线分析,血清 IFN-α 和 IL-33 浓度作为 1 型 AIP 和/或 IgG4-RD 标志物的诊断性能与血清 IgG4 浓度相当。泼尼松龙治疗诱导缓解显著降低了这些细胞因子的血清浓度。我们得出结论,血清 IFN-α 和 IL-33 浓度可以作为 1 型 AIP 和 IgG4-RD 的有用生物标志物。