医学
哮喘
加药
封锁
炎症
临床试验
免疫学
气道高反应性
重症监护医学
生物信息学
精密医学
个性化医疗
哮喘管理
选择(遗传算法)
试验药物
过敏性哮喘
支气管收缩
奥马佐单抗
临床实习
气道
适应性反应
临床研究阶段
作者
Maral Ranjbar,Christiane E. Whetstone,Ravneet K. Hansi,Fatemeh Sadeghi,Gail M. Gauvreau
标识
DOI:10.1080/13543784.2026.2619605
摘要
Early-phase studies confirm that alarmin blockade is safe, biologically relevant, and efficacious for improving airway inflammation across multiple asthma phenotypes. TSLP inhibition is an approved and clinically available therapy, while IL-33 and IL-25 remain in earlier development. Future progress will rely on optimized airway-focused dosing strategies such as biomarker-guided patient selection and genetic profiling, to achieve optimal personalized therapy. Anti-alarmin biologics are poised to redefine asthma management by addressing inflammation at the epithelial origin of common asthma triggers and advancing clinical care toward precision medicine.
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