Chmiel James F, Konstan Michael W
Division of Pediatric Pulmonology, Department of Pediatrics, Case Western Reserve University School of Medicine, 11100 Euclid Avenue, Cleveland, OH 44106, USA.
Clin Chest Med. 2007 Jun;28(2):331-46. doi: 10.1016/j.ccm.2007.02.002.
Cystic fibrosis lung disease is characterized by a self-propagating cycle of obstruction, infection, and inflammation. The inflammatory response, which accounts for the majority of the morbidity and mortality of the disease, begins early in life, becomes persistent, and is excessive relative to the bacterial burden. Therapies aimed at decreasing the inflammatory response represent a relatively new strategy for treatment. This article reviews the current state of the art of anti-inflammatory therapy in cystic fibrosis and introduces clinical trials that are underway.
囊性纤维化肺病的特征是梗阻、感染和炎症的自我传播循环。炎症反应是该疾病发病和死亡的主要原因,在生命早期就开始,持续存在,且相对于细菌负荷而言过度。旨在减少炎症反应的治疗方法是一种相对较新的治疗策略。本文综述了囊性纤维化抗炎治疗的当前技术水平,并介绍了正在进行的临床试验。