Paediatric section, Department of Surgery, Dentistry, Paediatrics, and Gynaecology, University of Verona, Verona, Italy.
Pediatr Allergy Immunol. 2020 Feb;31 Suppl 24:37-39. doi: 10.1111/pai.13162.
Asthmatic children usually reach good control of symptoms with a low-medium dose of inhaled corticosteroids (ICS), but approximately 5% has severe asthma. In this group of patients, when the diagnosis of severe asthma is confirmed, biologic agents have to be considered when there is no control of the symptoms despite conventional treatment with controllers according to guidelines. At present, the only biologic agent available in clinical practice for severe asthma treatment in children (6-18 years) is omalizumab. Mepolizumab has been recently approved by EMA for pediatric use. Reslizumab is a monoclonal antibody anti-IL-5 that has been approved for severe eosinophilic asthma treatment only in patients >12 years. Because of their action on specific molecular targets of the asthma pathophysiology, biologic agents are very promising therapeutic options for severe asthmatic patients based on individual endotypes.
哮喘儿童通常通过低-中剂量吸入皮质类固醇(ICS)就能很好地控制症状,但仍有约 5%的哮喘儿童为重症哮喘。对于这部分患者,当确诊为重症哮喘时,如果按照指南常规使用控制药物仍无法控制症状,则应考虑使用生物制剂。目前,在临床实践中,唯一可用于儿童(6-18 岁)重症哮喘治疗的生物制剂是奥马珠单抗。美泊利珠单抗最近已被欧洲药品管理局批准用于儿科使用。雷索利珠单抗是一种抗白细胞介素-5 的单克隆抗体,仅批准用于 12 岁以上的重度嗜酸性粒细胞性哮喘患者。由于它们针对哮喘病理生理学的特定分子靶点发挥作用,生物制剂为重症哮喘患者提供了非常有前途的治疗选择,基于个体化的表型。