4.5 Review

Club Cell Protein 16 (CC16) Augmentation: A Potential Disease-modifying Approach for Chronic Obstructive Pulmonary Disease (COPD)

Journal

EXPERT OPINION ON THERAPEUTIC TARGETS
Volume 20, Issue 7, Pages 869-883

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/14728222.2016.1139084

Keywords

Bronchoalveolar lavage fluid; CC10; CC16; chronic bronchitis; Club cells; COPD; emphysema; formyl peptide receptor-2; lipoxin A(4); lung inflammation; nuclear factor kappa B; phospholipase A(2); recombinant therapy; serum amyloid A; secretoglobin 1A1; small airway remodeling; toll-like receptor; uteroglobin

Funding

  1. United States Public Health Service
  2. National Institutes of Health under National Heart, Lung, and Blood Institute [HL063137, HL086814, HL111835, PO1 HL105339, P01 HL114501, AI111475-01]
  3. Flight Attendants Medical Research Institute [CIA123046, YFEL141004]
  4. Brigham and Women's Hospital-Lovelace Respiratory Research Institute Consortium
  5. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [P01HL114501, P01HL105339, R01HL063137, R21HL111835, R01HL086814] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI111475] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [R21ES025379] Funding Source: NIH RePORTER

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Introduction: 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. Areas Covered: 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. Expert Opinion: 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.

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