Laucho-Contreras Maria E, Polverino Francesca, Tesfaigzi Yohannes, Pilon Aprile, Celli Bartolome R, Owen Caroline A
a Division of Pulmonary and Critical Care Medicine , Brigham and Women's Hospital/Harvard Medical School , Boston , MA , USA.
b COPD Program , Lovelace Respiratory Research Institute , Albuquerque , NM , USA.
Expert Opin Ther Targets. 2016 Jul;20(7):869-83. doi: 10.1517/14728222.2016.1139084. Epub 2016 Feb 11.
Club cell protein 16 (CC16) is the most abundant protein in bronchoalveolar lavage fluid. CC16 has anti-inflammatory properties in smoke-exposed lungs, and chronic obstructive pulmonary disease (COPD) is associated with CC16 deficiency. Herein, we explored whether CC16 is a therapeutic target for COPD.
We reviewed the literature on the factors that regulate airway CC16 expression, its biologic functions and its protective activities in smoke-exposed lungs using PUBMED searches. We generated hypotheses on the mechanisms by which CC16 limits COPD development, and discuss its potential as a new therapeutic approach for COPD.
CC16 plasma and lung levels are reduced in smokers without airflow obstruction and COPD patients. In COPD patients, airway CC16 expression is inversely correlated with severity of airflow obstruction. CC16 deficiency increases smoke-induced lung pathologies in mice by its effects on epithelial cells, leukocytes, and fibroblasts. Experimental augmentation of CC16 levels using recombinant CC16 in cell culture systems, plasmid and adenoviral-mediated over-expression of CC16 in epithelial cells or smoke-exposed murine airways reduces inflammation and cellular injury. Additional studies are necessary to assess the efficacy of therapies aimed at restoring airway CC16 levels as a new disease-modifying therapy for COPD patients.
克拉拉细胞蛋白16(CC16)是支气管肺泡灌洗液中含量最丰富的蛋白质。CC16在暴露于烟雾的肺中具有抗炎特性,而慢性阻塞性肺疾病(COPD)与CC16缺乏有关。在此,我们探讨了CC16是否为COPD的治疗靶点。
我们使用PUBMED检索,回顾了关于调节气道CC16表达的因素、其生物学功能及其在暴露于烟雾的肺中的保护活性的文献。我们提出了关于CC16限制COPD发展机制的假设,并讨论了其作为COPD新治疗方法的潜力。
在无气流受限的吸烟者和COPD患者中,CC16的血浆和肺水平降低。在COPD患者中,气道CC16表达与气流受限的严重程度呈负相关。CC16缺乏通过其对上皮细胞、白细胞和成纤维细胞的影响增加了小鼠烟雾诱导的肺部病变。在细胞培养系统中使用重组CC16、在上皮细胞或暴露于烟雾的小鼠气道中通过质粒和腺病毒介导的CC16过表达来实验性提高CC16水平,可减轻炎症和细胞损伤。需要进一步研究来评估旨在恢复气道CC16水平作为COPD患者新的疾病改善疗法的疗效。