Department of Medical, Stridon Clinical Research, Richmond Upon Thames, London, UK.
Department of Public Health, Policy & Systems, Institute of Population Health, University of Liverpool, Liverpool, Merseyside, UK.
Int J Chron Obstruct Pulmon Dis. 2023 Apr 3;18:447-457. doi: 10.2147/COPD.S393540. eCollection 2023.
COPD (chronic obstructive pulmonary disease) is a major public health concern associated with significant morbidity and mortality worldwide. Current therapeutic guidelines for this disease recommend starting with an inhaled bronchodilator, stepping up to combination therapy as necessary, and/or adding inhaled corticosteroids as symptoms and airflow obstruction progress. However, no drug therapy exists to stop disease progression. The mechanistic definition underlying COPD pathogenesis remains poorly understood, it is generally accepted that oxidative stress and the altered immune response of low-grade airway inflammation are major factors contributing to COPD development. There are several potential therapeutic targets that are currently under investigation, including immune regulatory pathways in inflammation and lung-associated steroid resistance induced by oxidative stress signaling cascades. Patients with COPD have increased levels of inflammatory mediators, including lipid and peptide mediators, as well as a network of cytokines and chemokines that maintain inflammatory immune response and recruit circulating cells into the lungs. Many of these pro-inflammatory mediators are regulated by nuclear factor-kappaB (NF-κB) and mitogen-activated protein kinases (MAPKs), such as p38 MAPK. Increased oxidative stress is a key driving mechanism in perpetuating inflammation and lung injury. Furthermore, many proteases that degrade elastin fibres are secreted by airway resident infiltrating immune cells in COPD patients. In this perspective, we discuss novel aspects of signaling pathway activation in the context of inflammation and oxidative stress, and the broad view of potential effective pharmacotherapies that target the underlying mechanistic disease process in COPD.
COPD(慢性阻塞性肺疾病)是一个全球性的重大公共卫生问题,与高发病率和高死亡率相关。目前针对这种疾病的治疗指南建议从吸入支气管扩张剂开始,如果有必要,可升级为联合治疗,或随着症状和气流阻塞的进展,加用吸入性皮质类固醇。然而,目前尚无药物疗法可阻止疾病进展。COPD 发病机制的机制定义仍了解甚少,人们普遍认为氧化应激和低水平气道炎症的免疫反应改变是导致 COPD 发展的主要因素。目前有几个潜在的治疗靶点正在研究中,包括炎症中的免疫调节途径和氧化应激信号级联诱导的肺相关类固醇耐药性。COPD 患者的炎症介质水平升高,包括脂质和肽介质,以及细胞因子和趋化因子网络,这些都维持着炎症免疫反应,并将循环细胞招募到肺部。许多这些促炎介质受核因子-κB(NF-κB)和丝裂原活化蛋白激酶(MAPKs),如 p38 MAPK 的调节。氧化应激增加是炎症和肺损伤持续存在的关键驱动机制。此外,许多在 COPD 患者气道驻留浸润免疫细胞中分泌的弹性纤维蛋白酶。在这方面,我们讨论了炎症和氧化应激背景下信号通路激活的新方面,以及针对 COPD 潜在机制疾病过程的广泛有效药物治疗的观点。