Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Harvard Medical School, Boston, Massachusetts.
Arthritis Rheumatol. 2021 Jul;73(7):1334-1340. doi: 10.1002/art.41640. Epub 2021 May 31.
Canakinumab is a human anti-interleukin-1β (anti-IL-1β) blocking agent that effectively neutralizes IL-1β-mediated signaling for treatment of systemic juvenile idiopathic arthritis (JIA). While many patients have dramatic clinical response to IL-1 blockade, approximately one-third fail to respond, but there are currently no validated clinical or immunologic predictors of response. We undertook this study to characterize distinct gene signatures for treatment response and nonresponse to canakinumab in systemic JIA patients.
We performed a secondary analysis of whole-blood gene expression microarrays using blood samples obtained from healthy controls and systemic JIA patients at baseline and on day 3 after canakinumab treatment (GEO accession no. GSE80060). Patients were considered strong clinical responders if they met the ACR90 response (exhibited ≥90% improvement in the American College of Rheumatology [ACR] JIA response criteria; nonresponders were those who met ACR30 [exhibiting ≤30% improvement in the ACR JIA response criteria]). A random-effects model with patient identity as the random variable was used for differential expression analysis.
We identified a distinct gene expression signature in patients with a strong clinical response to canakinumab treatment as compared to nonresponders, mediated by up-regulation of neutrophil- and IL-1-associated genes and characterized by increasing divergence from control transcriptomes with increasing clinical response. We also identified a signature including up-regulated CD163 expression that was associated with canakinumab nonresponse. Intriguingly, canakinumab treatment induced either up- or down-regulation of type I interferon (IFN) genes, independent of clinical response.
Here, we identify a gene signature in systemic JIA patients prior to receiving treatment that distinguishes strong responders to canakinumab from nonresponders. Further prospective studies are needed to assess the utility of these insights for treatment decisions in systemic JIA and to track the association of up-regulated type I IFN signatures with systemic JIA complications.
卡那单抗是一种人源抗白细胞介素-1β(抗-IL-1β)阻断剂,可有效中和白细胞介素-1β介导的信号通路,用于治疗全身型幼年特发性关节炎(sJIA)。虽然许多患者对 IL-1 阻断治疗有明显的临床反应,但约有三分之一的患者反应不佳,但目前尚无有效的临床或免疫预测反应的指标。我们进行了这项研究,以确定全身型 JIA 患者对卡那单抗治疗有反应和无反应的独特基因特征。
我们对健康对照者和全身型 JIA 患者的全血基因表达微阵列进行了二次分析,这些患者在基线和卡那单抗治疗后第 3 天(GEO 注册号:GSE80060)采集了血液样本。如果患者符合 ACR90 反应(美国风湿病学会 [ACR] JIA 反应标准的改善≥90%;无反应者为 ACR30 反应[ACR JIA 反应标准的改善≤30%]),则被认为是强临床反应者。采用具有患者身份为随机变量的随机效应模型进行差异表达分析。
与无反应者相比,我们在对卡那单抗治疗有强临床反应的患者中发现了一个独特的基因表达特征,该特征是由中性粒细胞和白细胞介素-1 相关基因的上调介导的,并且随着临床反应的增加,与对照转录组的差异逐渐增大。我们还发现了一个包括上调 CD163 表达的特征,该特征与卡那单抗无反应有关。有趣的是,卡那单抗治疗诱导了 I 型干扰素(IFN)基因的上调或下调,与临床反应无关。
在这里,我们在接受治疗前的全身型 JIA 患者中确定了一个基因特征,该特征可将对卡那单抗的强反应者与无反应者区分开来。需要进一步的前瞻性研究来评估这些发现对全身型 JIA 治疗决策的效用,并跟踪上调的 I 型 IFN 特征与全身型 JIA 并发症的关联。