Pijnenburg Mariëlle W, Frey Urs, De Jongste Johan C, Saglani Sejal
Dept of Paediatrics, Division of Respiratory Medicine and Allergology, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands
University Children's Hospital Basel (UKBB), Basel, Switzerland.
Eur Respir J. 2022 Jun 9;59(6). doi: 10.1183/13993003.00731-2021. Print 2022 Jun.
In the pathogenesis of asthma in children there is a pivotal role for a type 2 inflammatory response to early life exposures or events. Interactions between infections, atopy, genetic susceptibility and environmental exposures (such as farmyard environment, air pollution and tobacco smoke exposure) influence the development of wheezing illness and the risk of progression to asthma. The immune system, lung function and the microbiome in gut and airways develop in parallel, and dysbiosis of the microbiome may be a critical factor in asthma development. Increased infant weight gain and preterm birth are other risk factors for development of asthma and reduced lung function. The complex interplay between these factors explains the heterogeneity of asthma in children. Subgroups of patients can be identified as phenotypes, based on clinical parameters, or endotypes, based on a specific pathophysiological mechanism. Paediatric asthma phenotypes and endotypes may ultimately help to improve diagnosis of asthma, prediction of asthma development and treatment of individual children, based on clinical, temporal, developmental or inflammatory characteristics. Unbiased, data-driven clustering, using a multidimensional or systems biology approach may be needed to better define phenotypes. The present knowledge on inflammatory phenotypes of childhood asthma has now been successfully applied in the treatment with biologicals of children with severe therapy-resistant asthma, and it is to be expected that more personalised treatment options may become available.
在儿童哮喘的发病机制中,对早期生活暴露或事件的2型炎症反应起着关键作用。感染、特应性、遗传易感性和环境暴露(如农场环境、空气污染和接触烟草烟雾)之间的相互作用会影响喘息性疾病的发展以及进展为哮喘的风险。免疫系统、肺功能以及肠道和气道中的微生物群是并行发育的,微生物群失调可能是哮喘发展的关键因素。婴儿体重增加和早产是哮喘发展和肺功能降低的其他危险因素。这些因素之间复杂的相互作用解释了儿童哮喘的异质性。根据临床参数可将患者亚组确定为表型,或根据特定的病理生理机制确定为内型。儿童哮喘的表型和内型最终可能有助于基于临床、时间、发育或炎症特征改善哮喘的诊断、哮喘发展的预测以及对个体儿童的治疗。可能需要采用多维或系统生物学方法进行无偏倚的数据驱动聚类,以更好地定义表型。目前关于儿童哮喘炎症表型的知识现已成功应用于重度难治性哮喘儿童的生物制剂治疗中,预计会有更多个性化的治疗选择出现。