Successful Use of Anakinra in a Patient with IL-10R Beta Deficiency: A Case Report.

IF 1.1 4区 医学 Q4 ALLERGY Pediatric Allergy Immunology and Pulmonology Pub Date : 2025-02-14 DOI:10.1089/ped.2024.0116
Selcuk Dogan, Ridvan Selen, Ferda Ozbay Hosnut, Semanur Ozdel, Figen Dogu, Aydan Ikinciogullari, Caner Aytekin
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Abstract

Background: Interleukin-10 (IL-10) is a crucial anti-inflammatory cytokine essential for maintaining immune homeostasis, particularly in the gastrointestinal system. Defects in the IL-10 signaling pathway, including mutations in interlaukin-10 receptor (IL-10R) beta, have been implicated in early-onset inflammatory bowel disease (IBD), often resistant to conventional treatments. Case Presentation: We report a 1.5-month-old male patient with IL-10R beta deficiency presenting with fever, vomiting, malnutrition, and sepsis. Despite normal initial evaluations, persistent fever and elevated inflammatory markers prompted the initiation of anakinra, an interleukin-1 receptor antagonist. Genetic testing confirmed a homozygous deletion in the IL10RB gene. Anakinra led to significant clinical improvement, including weight gain and symptom resolution. The patient was enrolled in an allogeneic hematopoietic stem cell transplantation (HSCT) program and successfully received HSCT from an HLA-matched related donor. Discussion: IL-10R beta deficiency presents with severe and early-onset symptoms, often unresponsive to standard IBD therapies. Anakinra has shown promise in bridging to HSCT by reducing inflammation and improving clinical outcomes in patients with IL-10 pathway defects. This case highlights the effectiveness of anakinra as a treatment strategy in severe, refractory IBD associated with IL-10R beta deficiency and underscores the importance of genetic testing for accurate diagnosis and treatment planning. Conclusion: Anakinra may provide significant clinical benefits in patients with IL-10R beta deficiency, serving as a bridge to definitive treatment with HSCT. Early genetic diagnosis and targeted therapy are crucial for managing this challenging condition.

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背景:白细胞介素-10(IL-10)是一种重要的抗炎细胞因子,对维持免疫平衡至关重要,尤其是在胃肠系统中。IL-10信号通路的缺陷,包括白介素-10受体(IL-10R)β的突变,与早发性炎症性肠病(IBD)有关,这种疾病通常对常规治疗具有抗药性。病例介绍:我们报告了一名 1.5 个月大的 IL-10R beta 缺乏症男性患者,患者表现为发热、呕吐、营养不良和败血症。尽管初步评估结果正常,但持续发热和炎症指标升高促使患者开始使用白介素-1受体拮抗剂阿那金拉(anakinra)。基因检测证实患者的 IL10RB 基因存在同基因缺失。Anakinra 带来了显著的临床改善,包括体重增加和症状缓解。患者加入了异基因造血干细胞移植(HSCT)计划,并成功接受了HLA匹配的亲缘供体的造血干细胞移植。讨论IL-10R beta缺乏症会出现严重的早发症状,通常对标准IBD疗法无反应。Anakinra 可减轻 IL-10 通路缺陷患者的炎症反应并改善其临床疗效,因此有望成为造血干细胞移植的桥接药物。本病例强调了 Anakinra 作为一种治疗策略对伴有 IL-10R beta 缺乏症的重症难治性 IBD 的有效性,并强调了基因检测对准确诊断和治疗计划的重要性。结论Anakinra 可为 IL-10R beta 缺乏症患者带来显著的临床疗效,成为造血干细胞移植明确治疗的桥梁。早期基因诊断和靶向治疗对于治疗这种具有挑战性的疾病至关重要。
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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
23
审稿时长
>12 weeks
期刊介绍: Pediatric Allergy, Immunology, and Pulmonology is a peer-reviewed journal designed to promote understanding and advance the treatment of respiratory, allergic, and immunologic diseases in children. The Journal delivers original translational, clinical, and epidemiologic research on the most common chronic illnesses of children—asthma and allergies—as well as many less common and rare diseases. It emphasizes the developmental implications of the morphological, physiological, pharmacological, and sociological components of these problems, as well as the impact of disease processes on families. Pediatric Allergy, Immunology, and Pulmonology coverage includes: -Functional and genetic immune deficiencies- Interstitial lung diseases- Both common and rare respiratory, allergic, and immunologic diseases- Patient care- Patient education research- Public health policy- International health studies
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