McClean Nathaniel, Hasday Jeffery D, Shapiro Paul
Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, MD, United States.
Department of Medicine, Division of Pulmonary Medicine, University of Maryland School of Medicine, Baltimore, MD, United States.
Adv Pharmacol. 2023;98:145-178. doi: 10.1016/bs.apha.2023.04.004. Epub 2023 May 3.
Current therapies to mitigate inflammatory responses involved in airway remodeling and associated pathological features of asthma and chronic obstructive pulmonary disease (COPD) are limited and largely ineffective. Inflammation and the release of cytokines and growth factors activate kinase signaling pathways that mediate changes in airway mesenchymal cells such as airway smooth muscle cells and lung fibroblasts. Proliferative and secretory changes in mesenchymal cells exacerbate the inflammatory response and promote airway remodeling, which is often characterized by increased airway smooth muscle mass, airway hyperreactivity, increased mucus secretion, and lung fibrosis. Thus, inhibition of relevant kinases has been viewed as a potential therapeutic approach to mitigate the debilitating and, thus far, irreversible airway remodeling that occurs in asthma and COPD. Despite FDA approval of several kinase inhibitors for the treatment of proliferative disorders, such as cancer and inflammation associated with rheumatoid arthritis and ulcerative colitis, none of these drugs have been approved to treat asthma or COPD. This review will provide a brief overview of the role kinases play in the pathology of asthma and COPD and an update on the status of kinase inhibitors currently in clinical trials for the treatment of obstructive pulmonary disease. In addition, potential issues associated with the current kinase inhibitors, which have limited their success as therapeutic agents in treating asthma or COPD, and alternative approaches to target kinase functions will be discussed.
目前用于减轻气道重塑以及哮喘和慢性阻塞性肺疾病(COPD)相关病理特征中炎症反应的疗法有限,且大多无效。炎症以及细胞因子和生长因子的释放会激活激酶信号通路,这些通路介导气道间充质细胞(如气道平滑肌细胞和肺成纤维细胞)的变化。间充质细胞的增殖和分泌变化会加剧炎症反应并促进气道重塑,其特征通常为气道平滑肌质量增加、气道高反应性、黏液分泌增加和肺纤维化。因此,抑制相关激酶被视为一种潜在的治疗方法,以减轻哮喘和COPD中出现的使人衰弱且迄今为止不可逆的气道重塑。尽管美国食品药品监督管理局(FDA)已批准多种激酶抑制剂用于治疗增殖性疾病,如癌症以及与类风湿性关节炎和溃疡性结肠炎相关的炎症,但这些药物均未被批准用于治疗哮喘或COPD。本综述将简要概述激酶在哮喘和COPD病理过程中的作用,以及目前用于治疗阻塞性肺疾病的激酶抑制剂的临床试验现状。此外,还将讨论当前激酶抑制剂存在的、限制其在治疗哮喘或COPD中取得成功的潜在问题,以及靶向激酶功能的替代方法。