JAK inhibitors in refractory juvenile rheumatic diseases: Efficacy, tolerance and type-I interferon profiling, a single center retrospective study

IF 7.9 1区 医学 Q1 IMMUNOLOGY Journal of autoimmunity Pub Date : 2024-05-25 DOI:10.1016/j.jaut.2024.103248
Marie Solignac , Natalia Cabrera , Marine Fouillet-Desjonqueres , Agnes Duquesne , Audrey Laurent , Anne-Perrine Foray , Sebastien Viel , Franck Zekre , Alexandre Belot
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Abstract

Objectives

Janus Kinase inhibitors (JAKi) are a new class of drugs available for pediatric rheumatic diseases.

This study aimed to describe the safety and effectiveness of JAKi in these diseases, with a focus on longitudinal interferon-stimulated genes (ISG) assessment.

Methods

We present a single-center retrospective study of children with refractory pediatric rheumatic diseases including connective tissue diseases, monogenic type I interferonopathies or juvenile idiopathic arthritis, receiving JAKi. According to physicians’ assessment, treatment effectiveness was classified at 12 months as a complete response in the total absence of disease activity, partial response in case of significant (>50%) but incomplete improvement or no response in the case of non-response or improvement of less than 50% of the clinical and biological parameters. ISG were monitored longitudinally using Nanostring technology.

Results

- 22 children were retrospectively included in this study, treated either by baricitinib or ruxolitinib. Complete response was achieved at 12 months in 9/22 (41%) patients. 6/22 (27%) patients were non-responders and treatment had been discontinued in five of them. Within the interferon (IFN)-related diseases group, ISG-score was significantly reduced 12 months after JAKi onset (p = 0.0068). At 12 months, daily glucocorticoid doses had been reduced with a median dose of 0.16 mg/kg/day (IQR 0.11; 0.33) (p = 0.0425). 7/22 (32%) patients had experienced side effects, infections being the most common. Increase of the body mass index was also recorded in children in the first 6 months of treatment.

Conclusion

JAKi represent a promising treatment of immune-mediated pediatric diseases, enabling to decrease type-I IFN transcriptomic signature in responding patients, especially in the context of juvenile dermatomyositis. JAKi represent steroid-sparing drugs but they induce metabolic changes linked to weight gain, posing a concern in the treatment of young patients and teenagers. More data are required to define the efficacy and safety of JAKi in the management of refractory pediatric rheumatic diseases.

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JAK 抑制剂治疗难治性幼年风湿病:单中心回顾性研究:疗效、耐受性和I型干扰素分析
本研究旨在描述JAKi治疗这些疾病的安全性和有效性,重点关注干扰素刺激基因(ISG)的纵向评估。方法--我们对接受JAKi治疗的难治性小儿风湿病(包括结缔组织病、单基因I型干扰素病或幼年特发性关节炎)患儿进行了一项单中心回顾性研究。根据医生的评估,12 个月后的治疗效果分为完全应答(完全没有疾病活动)、部分应答(有明显改善(50%)但不完全)或无应答(无应答或临床和生物学参数改善不足 50%)。本研究回顾性纳入了22名儿童,他们接受了巴利昔尼或鲁希替尼治疗。9/22(41%)名患者在12个月后获得完全应答。6/22(27%)名患者无应答,其中5名患者已停止治疗。在干扰素(IFN)相关疾病组中,ISG评分在JAKi开始治疗12个月后显著降低(p = 0.0068)。12 个月时,糖皮质激素的日剂量有所减少,中位剂量为 0.16 毫克/千克/天(IQR 0.11; 0.33)(p = 0.0425)。7/22(32%)名患者出现了副作用,其中最常见的是感染。结论--JAKi是一种治疗免疫介导的儿科疾病的有效药物,能减少应答患者的I型IFN转录组特征,尤其是在幼年皮肌炎的治疗中。JAKi 是一种节省类固醇的药物,但它会诱发与体重增加有关的代谢变化,在治疗年轻患者和青少年时令人担忧。在治疗难治性小儿风湿病时,还需要更多数据来确定JAKi的疗效和安全性。
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来源期刊
Journal of autoimmunity
Journal of autoimmunity 医学-免疫学
CiteScore
27.90
自引率
1.60%
发文量
117
审稿时长
17 days
期刊介绍: The Journal of Autoimmunity serves as the primary publication for research on various facets of autoimmunity. These include topics such as the mechanism of self-recognition, regulation of autoimmune responses, experimental autoimmune diseases, diagnostic tests for autoantibodies, as well as the epidemiology, pathophysiology, and treatment of autoimmune diseases. While the journal covers a wide range of subjects, it emphasizes papers exploring the genetic, molecular biology, and cellular aspects of the field. The Journal of Translational Autoimmunity, on the other hand, is a subsidiary journal of the Journal of Autoimmunity. It focuses specifically on translating scientific discoveries in autoimmunity into clinical applications and practical solutions. By highlighting research that bridges the gap between basic science and clinical practice, the Journal of Translational Autoimmunity aims to advance the understanding and treatment of autoimmune diseases.
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