Department of Health Sciences, University "Magna Græcia" of Catanzaro, Catanzaro, Italy.
Department of Medicine, Surgery and Dentistry, University of Salerno, Salerno, Italy.
Drug Des Devel Ther. 2021 Mar 23;15:1275-1284. doi: 10.2147/DDDT.S300988. eCollection 2021.
Among the various members of the mitogen-activated protein kinase (MAPK) family, p38 MAPK subgroup is the most involved in airway and lung inflammation underlying asthma and chronic obstructive pulmonary disease (COPD). In particular, several environmental agents including aeroallergens, cigarette smoke, airborne pollutants, viral and bacterial pathogens activate the p38α isoform which in turn up-regulates the expression of multiple proinflammatory cytokines and chemokines, as well as the production of some fibrogenic factors. Therefore, p38 MAPK-induced bronchial inflammation and remodelling significantly contribute to the development, persistence and amplification of airflow limitation, which is the hallmark of asthma and COPD. Such advances in our understanding of p38 role in the pathobiology of the above widespread, chronic obstructive respiratory diseases, have led to consider p38 MAPK as a suitable molecular target for novel treatment strategies. Indeed, many studies have been carried out in both animal and clinical settings, with the aim of evaluating the potential therapeutic effects of p38 MAPK inhibitors in both asthma and COPD.
在丝裂原活化蛋白激酶(MAPK)家族的众多成员中,p38 MAPK 亚组与哮喘和慢性阻塞性肺疾病(COPD)相关的气道和肺部炎症关系最为密切。特别是,包括气传过敏原、香烟烟雾、空气污染物、病毒和细菌病原体在内的几种环境因子激活了 p38α 同工型,进而上调了多种促炎细胞因子和趋化因子的表达,以及一些成纤维因子的产生。因此,p38 MAPK 诱导的支气管炎症和重塑显著促进了气流受限的发展、持续和放大,这是哮喘和 COPD 的标志。我们对 p38 在上述广泛的慢性阻塞性呼吸道疾病的病理生物学中的作用的理解的进展,使得 p38 MAPK 被认为是新型治疗策略的合适分子靶标。事实上,已经在动物和临床环境中进行了许多研究,目的是评估 p38 MAPK 抑制剂在哮喘和 COPD 中的潜在治疗效果。