Perikleous Evanthia P, Steiropoulos Paschalis, Nena Evangelia, Paraskakis Emmanouil
Medical School, Democritus University of Thrace, 68100 Alexandroupoli, Greece.
Department of Pneumonology, University General Hospital of Alexandroupolis, Democritus University of Thrace, 68100 Alexandroupoli, Greece.
J Pers Med. 2022 Jun 18;12(6):999. doi: 10.3390/jpm12060999.
Undeniably, childhood asthma is a multifactorial and heterogeneous chronic condition widespread in children. Its management, especially of the severe form refractory to standard therapy remains challenging. Over the past decades, the development of biologic agents and their subsequent approval has provided an advanced and very promising treatment alternative, eventually directing toward a successful precision medicine approach. The application of currently approved add-on treatments for severe asthma in children, namely omalizumab, mepolizumab, benralizumab, dupilumab, and tezepelumab have been shown to be effective in terms of asthma control and exacerbation rate. However, to date, information is still lacking regarding its long-term use. As a result, data are frequently extrapolated from adult studies. Thus, the selection of the appropriate biologic agent, the potential predictors of good asthma response, and the long-term outcome in the pediatric population are still to be further investigated. The aim of the present study was to provide an overview of the current status of the latest evidence about all licensed monoclonal antibodies (mAbs) that have emerged and been applied to the field of asthma management. The innovative future targets are also briefly discussed.
不可否认,儿童哮喘是一种多因素且异质性的慢性疾病,在儿童中广泛存在。其管理,尤其是对标准治疗难治的严重形式,仍然具有挑战性。在过去几十年中,生物制剂的开发及其随后的获批提供了一种先进且非常有前景的治疗选择,最终朝着成功的精准医学方法发展。目前批准用于儿童重度哮喘的附加治疗药物,即奥马珠单抗、美泊利单抗、贝那利珠单抗、度普利尤单抗和tezepelumab,在哮喘控制和加重率方面已显示出有效性。然而,迄今为止,关于其长期使用的信息仍然缺乏。因此,数据经常从成人研究中推断得出。因此,合适生物制剂的选择、哮喘良好反应的潜在预测因素以及儿科人群中的长期结局仍有待进一步研究。本研究的目的是概述已出现并应用于哮喘管理领域的所有许可单克隆抗体(mAb)的最新证据的现状。还简要讨论了创新的未来靶点。