Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Division of Allergy and Immunology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Ann Allergy Asthma Immunol. 2024 Jan;132(1):13-20. doi: 10.1016/j.anai.2023.08.597. Epub 2023 Aug 29.
To evaluate the current evidence, its limitations, and future research directions for the use of biologics in pediatric asthma, with a particular focus on the potential use of biologics to prevent pediatric asthma and equity issues in access to biologic treatment and research participation.
PubMed articles about the use of biologics in pediatric asthma were searched up to May 2023.
Recent (2019-2023) original research articles and reviews were prioritized.
Although there are now 5 U.S. Food and Drug Administration-approved biologics for use in pediatric asthma, there are important knowledge gaps that ongoing research seeks to address, which include (1) the long-term efficacy and safety of using biologics in children, (2) the comparative efficacy of different biologics, (3) multi-omics-based classification of asthma endotypes and phenotypes in children to find potential new therapeutic targets and enable identification and validation of new biomarkers that may predict and help monitor response to treatment, and (4) whether starting biologics in early childhood can modify the natural history of asthma and potentially prevent asthma development.
To promote equitable access to biologics and optimize asthma outcomes, future research should recruit patients across the full spectrum of socioeconomic and racial/ethnic backgrounds. Large-scale national and international collaborations between asthma researchers and clinicians are also necessary to fully understand the role of biologics in pediatric asthma.
评估生物制剂在儿科哮喘中的应用的现有证据、其局限性以及未来的研究方向,特别关注生物制剂预防儿科哮喘的潜在用途以及在获得生物治疗和参与研究方面的公平问题。
截至 2023 年 5 月,在 PubMed 上搜索了关于生物制剂在儿科哮喘中应用的文章。
优先考虑了最近(2019-2023 年)的原始研究文章和综述。
尽管现在有 5 种美国食品和药物管理局批准的生物制剂可用于儿科哮喘,但仍存在重要的知识空白,正在进行的研究旨在解决这些问题,包括:(1)在儿童中使用生物制剂的长期疗效和安全性;(2)不同生物制剂的比较疗效;(3)基于多组学的儿童哮喘表型和表型分类,以寻找潜在的新治疗靶点,并能够识别和验证可能预测和有助于监测治疗反应的新生物标志物;(4)在儿童早期开始使用生物制剂是否可以改变哮喘的自然史并可能预防哮喘的发生。
为了促进公平获得生物制剂并优化哮喘结局,未来的研究应招募来自各种社会经济和种族/民族背景的患者。哮喘研究人员和临床医生之间还需要进行大规模的国家和国际合作,以充分了解生物制剂在儿科哮喘中的作用。