哮喘
医学
粘液
气道高反应性
临床试验
气道
囊性纤维化
疾病
免疫学
重症监护医学
内科学
生物
外科
生态学
作者
Samantha K. Hamrick,Michael A. Thompson,Vincent M. Rotello,Y. S. Prakash,Christina M. Pabelick
出处
期刊:American Journal of Physiology-lung Cellular and Molecular Physiology
[American Physical Society]
日期:2024-10-29
卷期号:327 (6): L964-L971
标识
DOI:10.1152/ajplung.00248.2024
摘要
Asthma is a heterogeneous chronic lung disease that affects nearly 340 million people globally. Airway hyperresponsiveness, remodeling (thickening and fibrosis), and mucus hypersecretion are some hallmarks of asthma. With several current treatments having serious side effects from long-term use and a proportion of patients with uncontrolled asthma, there is an urgent need for new therapies. With an increasing understanding of asthma pathophysiology, there is a recognized need to target therapies to specific cell types of the airway, which necessitates the identification of delivery systems that can overcome increased mucus and thickened airways. Nanoparticles (NPs) that are highly customizable (material, size, charge, and surface modification) are a potential solution for delivery systems of a wide variety of cargoes (nucleic acids, proteins, and/or small molecules), as well as sole therapeutics for asthma. However, there is a need to consider the safety of the NPs in terms of potential for inflammation, toxicity, nonspecific targets, and accumulation in organs. Ongoing clinical trials using NPs, some FDA-approved for therapeutics in other diseases, provide confidence regarding the potential safety and efficacy of NPs in asthma treatment. This review highlights the current state of the use of NPs in asthma, identifying opportunities for further improvements in NP design and utilization for targeting this chronic lung disease.
科研通智能强力驱动
Strongly Powered by AbleSci AI