Martin Alonso Aldara, Saglani Sejal
Inflammation, Repair and Development Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Respiratory Pediatrics, The Royal Brompton Hospital, London, United Kingdom.
Front Pediatr. 2017 Jul 5;5:154. doi: 10.3389/fped.2017.00154. eCollection 2017.
Although a rare disease, severe therapy-resistant asthma in children is a cause of significant morbidity and results in utilization of approximately 50% of health-care resources for asthma. Improving control for children with severe asthma is, therefore, an urgent unmet clinical need. As a group, children with severe asthma have severe and multiple allergies, steroid resistant airway eosinophilia, and significant structural changes of the airway wall (airway remodeling). Omalizumab is currently the only add-on therapy that is licensed for use in children with severe asthma. However, limitations of its use include ineligibility for approximately one-third of patients because of serum IgE levels outside the recommended range and lack of clinical efficacy in a further one-third. Pediatric severe asthma is thus markedly heterogeneous, but our current understanding of the different mechanisms underpinning various phenotypes is very limited. We know that there are distinctions between the factors that drive pediatric and adult disease since pediatric disease develops in the context of a maturing immune system and during lung growth and development. This review summarizes the current data that give insight into the pathophysiology of pediatric severe asthma and will highlight potential targets for novel therapies. It is apparent that in order to identify novel treatments for pediatric severe asthma, the challenge of undertaking mechanistic studies using age appropriate experimental models and airway samples from children needs to be accepted to allow a targeted approach of personalized medicine to be achieved.
尽管儿童重度难治性哮喘是一种罕见疾病,但它会导致严重的发病情况,并消耗约50%的哮喘医疗资源。因此,改善重度哮喘儿童的病情控制是一项迫切未得到满足的临床需求。重度哮喘儿童群体存在严重且多种过敏、类固醇抵抗性气道嗜酸性粒细胞增多以及气道壁显著的结构改变(气道重塑)。奥马珠单抗是目前唯一被批准用于重度哮喘儿童的附加治疗药物。然而,其使用存在局限性,约三分之一的患者因血清IgE水平超出推荐范围而不适用,另有三分之一的患者缺乏临床疗效。因此,儿童重度哮喘具有明显的异质性,但我们目前对支撑各种表型的不同机制的理解非常有限。我们知道,驱动儿童和成人疾病的因素存在差异,因为儿童疾病是在免疫系统成熟以及肺部生长发育的背景下发生的。本综述总结了当前有助于深入了解儿童重度哮喘病理生理学的数据,并将突出新型疗法的潜在靶点。显然,为了确定儿童重度哮喘的新型治疗方法,需要接受使用适合年龄的实验模型和儿童气道样本进行机制研究的挑战,以便实现个性化医疗的靶向方法。