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Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections.
Hisert, Katherine B; Heltshe, Sonya L; Pope, Christopher; Jorth, Peter; Wu, Xia; Edwards, Rachael M; Radey, Matthew; Accurso, Frank J; Wolter, Daniel J; Cooke, Gordon; Adam, Ryan J; Carter, Suzanne; Grogan, Brenda; Launspach, Janice L; Donnelly, Seamas C; Gallagher, Charles G; Bruce, James E; Stoltz, David A; Welsh, Michael J; Hoffman, Lucas R; McKone, Edward F; Singh, Pradeep K.
Affiliation
  • Hisert KB; 1 Department of Medicine.
  • Heltshe SL; 2 Department of Pediatrics.
  • Pope C; 2 Department of Pediatrics.
  • Jorth P; 3 Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, California.
  • Wu X; 4 Department of Genome Sciences.
  • Edwards RM; 5 Department of Radiology, and.
  • Radey M; 6 Department of Microbiology, University of Washington School of Medicine, Seattle, Washington.
  • Accurso FJ; 7 Department of Pediatrics, University of Colorado, Aurora, Colorado.
  • Wolter DJ; 2 Department of Pediatrics.
  • Cooke G; 8 St. Vincent's University Hospital, Dublin, Ireland.
  • Adam RJ; 9 Department of Internal Medicine, University of Iowa, Iowa City, Iowa; and.
  • Carter S; 8 St. Vincent's University Hospital, Dublin, Ireland.
  • Grogan B; 8 St. Vincent's University Hospital, Dublin, Ireland.
  • Launspach JL; 9 Department of Internal Medicine, University of Iowa, Iowa City, Iowa; and.
  • Donnelly SC; 10 Trinity College Dublin, Dublin, Ireland.
  • Gallagher CG; 8 St. Vincent's University Hospital, Dublin, Ireland.
  • Bruce JE; 4 Department of Genome Sciences.
  • Stoltz DA; 9 Department of Internal Medicine, University of Iowa, Iowa City, Iowa; and.
  • Welsh MJ; 9 Department of Internal Medicine, University of Iowa, Iowa City, Iowa; and.
  • Hoffman LR; 2 Department of Pediatrics.
  • McKone EF; 6 Department of Microbiology, University of Washington School of Medicine, Seattle, Washington.
  • Singh PK; 8 St. Vincent's University Hospital, Dublin, Ireland.
Am J Respir Crit Care Med ; 195(12): 1617-1628, 2017 06 15.
Article in En | MEDLINE | ID: mdl-28222269
ABSTRACT
RATIONALE Previous work indicates that ivacaftor improves cystic fibrosis transmembrane conductance regulator (CFTR) activity and lung function in people with cystic fibrosis and G551D-CFTR mutations but does not reduce density of bacteria or markers of inflammation in the airway. These findings raise the possibility that infection and inflammation may progress independently of CFTR activity once cystic fibrosis lung disease is established.

OBJECTIVES:

To better understand the relationship between CFTR activity, airway microbiology and inflammation, and lung function in subjects with cystic fibrosis and chronic airway infections.

METHODS:

We studied 12 subjects with G551D-CFTR mutations and chronic airway infections before and after ivacaftor. We measured lung function, sputum bacterial content, and inflammation, and obtained chest computed tomography scans. MEASUREMENTS AND MAIN

RESULTS:

Ivacaftor produced rapid decreases in sputum Pseudomonas aeruginosa density that began within 48 hours and continued in the first year of treatment. However, no subject eradicated their infecting P. aeruginosa strain, and after the first year P. aeruginosa densities rebounded. Sputum total bacterial concentrations also decreased, but less than P. aeruginosa. Sputum inflammatory measures decreased significantly in the first week of treatment and continued to decline over 2 years. Computed tomography scans obtained before and 1 year after ivacaftor treatment revealed that ivacaftor decreased airway mucous plugging.

CONCLUSIONS:

Ivacaftor caused marked reductions in sputum P. aeruginosa density and airway inflammation and produced modest improvements in radiographic lung disease in subjects with G551D-CFTR mutations. However, P. aeruginosa airway infection persisted. Thus, measures that control infection may be required to realize the full benefits of CFTR-targeting treatments.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Tract Infections / Quinolones / Cystic Fibrosis Transmembrane Conductance Regulator / Cystic Fibrosis / Aminophenols / Inflammation Limits: Adult / Female / Humans / Male Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Tract Infections / Quinolones / Cystic Fibrosis Transmembrane Conductance Regulator / Cystic Fibrosis / Aminophenols / Inflammation Limits: Adult / Female / Humans / Male Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2017 Document type: Article