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重度小儿哮喘治疗:度普利尤单抗。

Severe pediatric asthma therapy: Dupilumab.

作者信息

Ferrante Giuliana, Tenero Laura, Piazza Michele, Piacentini Giorgio

机构信息

Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, Pediatric Division, University of Verona, Verona, Italy.

Pediatric Division, University Hospital of Verona, Verona, Italy.

出版信息

Front Pediatr. 2022 Nov 22;10:963610. doi: 10.3389/fped.2022.963610. eCollection 2022.

Abstract

Severe asthma is a rare disease affecting <5% of children with asthma. This group of patients account for about 50% of the costs of healthcare for children with asthma. Nowadays, several biological agents are available for pediatric severe asthma. One of these is dupilumab, a monoclonal antibody against the Interleukin (IL)-4 receptor α-subunit that acts as an antagonist against both IL-4 and IL-13. Dupilumab binds the subunit of the IL-4 receptor, at the level of the subunit shared by the IL-13 receptor, blocking the inflammatory cascade of these two cytokines and the progression of the Th2-inflammatory pathway. The efficacy and safety of dupilumab have been investigated in recently published randomized controlled trials including pediatric patients with asthma. Currently, its use in asthma is approved in adults, adolescents, and children with severe asthma with type 2 inflammation, that are not controlled in spite of high-dose inhaled corticosteroids plus another maintenance drug. Studies are warranted for the evaluation of long-term treatment with dupilumab, including steroid sparing effect and discontinuation of treatment. Further research should also be planned in order to investigate dupilumab potential ability to interfere with the natural history of atopy since early childhood.

摘要

重度哮喘是一种罕见疾病,影响不到5%的哮喘儿童。这组患者约占哮喘儿童医疗保健费用的50%。如今,有几种生物制剂可用于治疗儿童重度哮喘。其中之一是度普利尤单抗,一种抗白细胞介素(IL)-4受体α亚基的单克隆抗体,它对IL-4和IL-13均起拮抗剂作用。度普利尤单抗在IL-13受体共享的亚基水平上结合IL-4受体的亚基,阻断这两种细胞因子的炎症级联反应以及Th2炎症途径的进展。度普利尤单抗的疗效和安全性已在最近发表的包括哮喘儿童患者在内的随机对照试验中进行了研究。目前,它被批准用于患有2型炎症的重度哮喘成人、青少年和儿童,这些患者尽管使用了高剂量吸入性糖皮质激素加另一种维持药物,但病情仍未得到控制。有必要开展研究以评估度普利尤单抗的长期治疗效果,包括其节省类固醇的作用和停药情况。还应计划进一步的研究,以调查度普利尤单抗从幼儿期开始干扰特应性自然病程的潜在能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64a1/9723147/9100b2536462/fped-10-963610-g001.jpg

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