Successful Treatment of Pediatric Generalized Pustular Psoriasis (GPP) with Spesolimab: 5 Case Reports and Evaluations of Circulating IL-36 Levels.

IF 4.2 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI:10.2147/JIR.S485077
Yunliu Chen, Zhaoyang Wang, Yuan Liang, Chunping Shen, Lei Jiao, Xin Xiang, Chaoyang Miao, Zigang Xu
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引用次数: 0

Abstract

Background: Generalized pustular psoriasis (GPP) is a rare, severe, and potentially life-threatening inflammatory cutaneous disease. IL-36 is a key treatment target in GPP. Spesolimab, a humanized monoclonal antibody of the IL-36 receptor, has demonstrated a good efficacy and a favorable safety profile in adults with GPP. However, data on its use in children are scarce.

Methods: We treated patients aged 4-12 years with GPP with a single dose of spesolimab. The Generalized Pustular Psoriasis Physician Global Assessment (GPPGA) total score, GPPGA pustulation sub-score, Generalized Pustular Psoriasis Area and Severity Index (GPPASI), and the Japanese Dermatological Association severity index for GPP were evaluated. The levels of IL-36α, IL-36β, and IL-36γ were detected by the magnetic bead-based immunoassays, and the levels of IL-17A, IL-17C, IFN-γ, TNF, IL-6, and IL-8 were measured by the Olink proximity extension assay technology.

Results: We included five patients (four boys and one girl) with a median age was 6.9 years old (range: 4.8 to 10.6 years), and a median age of onset of 1.7 years (range: 3 months-10 years and 5 months). After 1 week of spesolimab administration, all patients had a total GPPGA score of 0/1 and pustulation subscore of 0, all patients had a GPPASI of 50, and four patients had a GPPASI of 75. Meanwhile, plasma levels of IL-36α, IL-36β, IL-36γ, IL-17A, IL-17C, IFN-γ, TNF, IL-6, IL-8 all decreased, and those of IL-36α, IL-36β, IL-17A, IL-17C, and IL-6 were statistically significant. There was no recurrence after 2 to 8 months of treatment. No other adverse event was recorded apart from one patient who experienced an upper respiratory infection in the first week.

Conclusion: Spesolimab might be a prospective option for children aged 4 to 12 years.

斯派索利单抗成功治疗小儿泛发性脓疱型银屑病(GPP):5例病例报告和循环IL-36水平评估。
背景:泛发性脓疱型银屑病(GPP)是一种罕见、严重且可能危及生命的炎症性皮肤病。IL-36 是 GPP 的关键治疗靶点。Spesolimab是一种IL-36受体的人源化单克隆抗体,在成人GPP患者中表现出良好的疗效和安全性。然而,有关其在儿童中应用的数据却很少:我们对 4-12 岁的 GPP 患者进行了单剂量斯派索利单抗治疗。方法:我们对 4-12 岁的脓疱型银屑病患者进行了单剂量斯贝单抗治疗,评估了脓疱型银屑病医生总体评估(GPPGA)总分、脓疱型银屑病医生总体评估分值、脓疱型银屑病面积和严重程度指数(GPPASI)以及日本皮肤病协会的脓疱型银屑病严重程度指数。IL-36α、IL-36β和IL-36γ的水平由磁珠式免疫测定法检测,IL-17A、IL-17C、IFN-γ、TNF、IL-6和IL-8的水平由Olink近距离延伸检测技术测定:我们共收治了五名患者(四名男孩和一名女孩),中位年龄为 6.9 岁(范围:4.8 至 10.6 岁),中位发病年龄为 1.7 岁(范围:3 个月至 10 岁零 5 个月)。使用斯派索利单抗 1 周后,所有患者的 GPPGA 总分均为 0/1,脓疱亚分均为 0,所有患者的 GPPASI 均为 50,4 名患者的 GPPASI 均为 75。同时,血浆中的 IL-36α、IL-36β、IL-36γ、IL-17A、IL-17C、IFN-γ、TNF、IL-6、IL-8 水平均有所下降,其中 IL-36α、IL-36β、IL-17A、IL-17C 和 IL-6 的水平有统计学意义。治疗 2 至 8 个月后没有复发。除了一名患者在第一周出现上呼吸道感染外,没有其他不良反应记录:斯派索利单抗可能是4至12岁儿童的前瞻性选择。
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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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