School of Pharmacy and Pharmacology, University of Tasmania, Hobart, Australia.
Department of Molecular and Translational Science, Monash University, Clayton, Australia.
Inflammopharmacology. 2021 Feb;29(1):15-33. doi: 10.1007/s10787-020-00770-y. Epub 2020 Nov 5.
Asthma is a common, heterogeneous and serious disease, its prevalence has steadily risen in most parts of the world, and the condition is often inadequately controlled in many patients. Hence, there is a major need for new therapeutic approaches. Mild-to-moderate asthma is considered a T-helper cell type-2-mediated inflammatory disorder that develops due to abnormal immune responses to otherwise innocuous allergens. Prolonged exposure to allergens and persistent inflammation results in myofibroblast infiltration and airway remodelling with mucus hypersecretion, airway smooth muscle hypertrophy, and excess collagen deposition. The airways become hyper-responsive to provocation resulting in the characteristic wheezing and obstructed airflow experienced by patients. Extensive research has progressed the understanding of the underlying mechanisms and the development of new treatments for the management of asthma. Here, we review the basis of the disease, covering new areas such as the role of vascularisation and microRNAs, as well as associated potential therapeutic interventions utilising reports from animal and human studies. We also cover novel drug delivery strategies that are being developed to enhance therapeutic efficacy and patient compliance. Potential avenues to explore to improve the future of asthma management are highlighted.
哮喘是一种常见的、异质性的严重疾病,其在世界大多数地区的患病率稳步上升,许多患者的病情往往得不到充分控制。因此,人们迫切需要新的治疗方法。轻度至中度哮喘被认为是一种辅助性 T 细胞 2 型介导的炎症性疾病,是由于对原本无害的过敏原产生异常免疫反应而发展起来的。长时间暴露于过敏原和持续的炎症导致肌成纤维细胞浸润和气道重塑,伴有黏液过度分泌、气道平滑肌肥大和胶原过度沉积。气道对激发变得过度敏感,导致患者出现典型的喘息和气流受限。大量研究进展加深了对哮喘发病机制的理解,并为哮喘的治疗开发了新的治疗方法。在这里,我们回顾了疾病的基础,涵盖了血管生成和 microRNAs 的作用等新领域,以及利用动物和人类研究报告的相关潜在治疗干预措施。我们还介绍了正在开发的新型药物输送策略,以提高治疗效果和患者依从性。强调了探索改善哮喘管理未来的潜在途径。