Dept of Medicine, University of Alabama at Birmingham, Birmingham, AL 35244, USA.
Eur Respir J. 2011 Sep;38(3):721-7. doi: 10.1183/09031936.00173210. Epub 2011 Jan 13.
Significant airway remodelling is a major component of the increased morbidity and mortality observed in cystic fibrosis (CF) patients. These airways feature ongoing leukocytic inflammation and unrelenting bacterial infection. In contrast to acute bacterial pneumonia, CF infection is not cleared efficiently and the ensuing inflammatory response causes tissue damage. This structural damage is mainly a result of free proteolytic activity released by infiltrated neutrophils and macrophages. Major proteases in this disease are serine and matrix metalloproteases (MMPs). While the role of serine proteases, such as elastase, has been characterised in detail, there is emerging evidence that MMPs could play a key role in the pathogenesis of CF lung disease. This review summarises studies linking MMPs with CF lung disease and discusses the potential value of MMPs as future therapeutic targets in CF and other chronic lung diseases.
气道重塑是囊性纤维化(CF)患者发病率和死亡率增加的主要原因。这些气道存在持续的白细胞炎症和持续的细菌感染。与急性细菌性肺炎不同,CF 感染不能被有效清除,随之而来的炎症反应会导致组织损伤。这种结构损伤主要是浸润的中性粒细胞和巨噬细胞释放的游离蛋白水解酶活性引起的。在这种疾病中,主要的蛋白酶是丝氨酸蛋白酶和基质金属蛋白酶(MMPs)。虽然弹性蛋白酶等丝氨酸蛋白酶的作用已经得到详细描述,但越来越多的证据表明 MMPs 可能在 CF 肺部疾病的发病机制中发挥关键作用。这篇综述总结了将 MMPs 与 CF 肺部疾病联系起来的研究,并讨论了 MMPs 作为 CF 和其他慢性肺部疾病未来治疗靶点的潜在价值。