Lu Rufei, Munroe Melissa E, Guthridge Joel M, Bean Krista M, Fife Dustin A, Chen Hua, Slight-Webb Samantha R, Keith Michael P, Harley John B, James Judith A
Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104.
Departments of Medicine and Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104.
J Autoimmun. 2016 Nov;74:182-193. doi: 10.1016/j.jaut.2016.06.001. Epub 2016 Jun 20.
Systemic lupus erythematosus (SLE) is a complex autoimmune disease with a poorly understood preclinical stage of immune dysregulation and symptom accrual. Accumulation of antinuclear autoantibody (ANA) specificities is a hallmark of impending clinical disease. Yet, many ANA-positive individuals remain healthy, suggesting that additional immune dysregulation underlies SLE pathogenesis. Indeed, we have recently demonstrated that interferon (IFN) pathways are dysregulated in preclinical SLE. To determine if other forms of immune dysregulation contribute to preclinical SLE pathogenesis, we measured SLE-associated autoantibodies and soluble mediators in samples from 84 individuals collected prior to SLE classification (average timespan = 5.98 years), compared to unaffected, healthy control samples matched by race, gender, age (±5 years), and time of sample procurement. We found that multiple soluble mediators, including interleukin (IL)-5, IL-6, and IFN-γ, were significantly elevated in cases compared to controls more than 3.5 years pre-classification, prior to or concurrent with autoantibody positivity. Additional mediators, including innate cytokines, IFN-associated chemokines, and soluble tumor necrosis factor (TNF) superfamily mediators increased longitudinally in cases approaching SLE classification, but not in controls. In particular, levels of B lymphocyte stimulator (BLyS) and a proliferation-inducing ligand (APRIL) were comparable in cases and controls until less than 10 months pre-classification. Over the entire pre-classification period, random forest models incorporating ANA and anti-Ro/SSA positivity with levels of IL-5, IL-6, and the IFN-γ-induced chemokine, MIG, distinguished future SLE patients with 92% (±1.8%) accuracy, compared to 78% accuracy utilizing ANA positivity alone. These data suggest that immune dysregulation involving multiple pathways contributes to SLE pathogenesis. Importantly, distinct immunological profiles are predictive for individuals who will develop clinical SLE and may be useful for delineating early pathogenesis, discovering therapeutic targets, and designing prevention trials.
系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,其临床前免疫失调和症状累积阶段尚不清楚。抗核自身抗体(ANA)特异性的积累是即将发生临床疾病的标志。然而,许多ANA阳性个体仍保持健康,这表明SLE发病机制还存在其他免疫失调。事实上,我们最近证明,在临床前SLE中,干扰素(IFN)通路存在失调。为了确定其他形式的免疫失调是否有助于临床前SLE发病机制,我们测量了84名个体在SLE分类之前(平均时间跨度=5.98年)采集的样本中的SLE相关自身抗体和可溶性介质,并与按种族、性别、年龄(±5岁)和样本采集时间匹配的未受影响的健康对照样本进行比较。我们发现,与对照组相比,在分类前3.5年以上、自身抗体阳性之前或同时,包括白细胞介素(IL)-5、IL-6和IFN-γ在内的多种可溶性介质在病例中显著升高。包括先天细胞因子、IFN相关趋化因子和可溶性肿瘤坏死因子(TNF)超家族介质在内的其他介质在接近SLE分类的病例中纵向增加,但在对照组中没有增加。特别是,在分类前不到10个月时,病例组和对照组中的B淋巴细胞刺激因子(BLyS)和增殖诱导配体(APRIL)水平相当。在整个分类前期,将ANA和抗Ro/SSA阳性与IL-5、IL-6和IFN-γ诱导的趋化因子MIG水平纳入的随机森林模型,区分未来SLE患者的准确率为92%(±1.8%),而仅使用ANA阳性的准确率为78%。这些数据表明,涉及多种途径的免疫失调有助于SLE发病机制。重要的是,不同的免疫特征可预测哪些个体将发展为临床SLE,这可能有助于描绘早期发病机制、发现治疗靶点和设计预防试验。