Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections

被引:0
作者
Hisert, Katherine B. [1 ]
Heltshe, Sonya L. [2 ]
Pope, Christopher [2 ]
Jorth, Peter [6 ]
Wu, Xia [3 ]
Edwards, Rachael M. [4 ]
Radey, Matthew [5 ]
Accurso, Frank J. [7 ]
Wolter, Daniel J. [2 ]
Cooke, Gordon [8 ]
Adam, Ryan J. [9 ]
Carter, Suzanne [8 ]
Grogan, Brenda [8 ]
Launspach, Janice L. [9 ]
Donnelly, Seamas C. [10 ]
Gallagher, Charles G. [8 ]
Bruce, James E. [3 ]
Stoltz, David A. [9 ]
Welsh, Michael J.
Hoffman, Lucas R. [2 ,5 ]
McKone, Edward F. [8 ]
Singh, Pradeep K. [1 ,5 ]
机构
[1] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA USA
[4] Univ Washington, Sch Med, Dept Radiol, Seattle, WA 98195 USA
[5] Univ Washington, Sch Med, Dept Microbiol, Seattle, WA 98105 USA
[6] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[7] Univ Colorado, Dept Pediat, Aurora, CO USA
[8] St Vincents Univ Hosp, Dublin, Ireland
[9] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[10] Trinity Coll Dublin, Dublin, Ireland
基金
美国国家卫生研究院;
关键词
cystic fibrosis; Pseudomonas aeruginosa; ivacaftor; inflammation; PSEUDOMONAS-AERUGINOSA; POTENTIATOR IVACAFTOR; CFTR POTENTIATOR; DIVERSIFICATION; POPULATION; MUTATION;
D O I
10.1164/rccm.201609-1954OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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.
引用
收藏
页码:1617 / 1628
页数:12
相关论文
共 25 条
[1]   Effect of VX-770 in Persons with Cystic Fibrosis and the G551D-CFTR Mutation [J].
Accurso, Frank J. ;
Rowe, Steven M. ;
Clancy, J. P. ;
Boyle, Michael P. ;
Dunitz, Jordan M. ;
Durie, Peter R. ;
Sagel, Scott D. ;
Hornick, Douglas B. ;
Konstan, Michael W. ;
Donaldson, Scott H. ;
Moss, Richard B. ;
Pilewski, Joseph M. ;
Rubenstein, Ronald C. ;
Uluer, Ahmet Z. ;
Aitken, Moira L. ;
Freedman, Steven D. ;
Rose, Lynn M. ;
Mayer-Hamblett, Nicole ;
Dong, Qunming ;
Zha, Jiuhong ;
Stone, Anne J. ;
Olson, Eric R. ;
Ordonez, Claudia L. ;
Campbell, Preston W. ;
Ashlock, Melissa A. ;
Ramsey, Bonnie W. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (21) :1991-2003
[2]   Acute administration of ivacaftor to people with cystic fibrosis and a G551D-CFTR mutation reveals smooth muscle abnormalities [J].
Adam, Ryan J. ;
Hisert, Katherine B. ;
Dodd, Jonathan D. ;
Grogan, Brenda ;
Launspach, Janice L. ;
Barnes, Janel K. ;
Gallagher, Charles G. ;
Sieren, Jered P. ;
Gross, Thomas J. ;
Fischer, Anthony J. ;
Cavanaugh, Joseph E. ;
Hoffman, Eric A. ;
Singh, Pradeep K. ;
Welsh, Michael J. ;
McKone, Edward F. ;
Stoltz, David A. .
JCI INSIGHT, 2016, 1 (04)
[3]   Extensive diversification is a common feature of Pseudomonas aeruginosa populations during respiratory infections in cystic fibrosis [J].
Ashish, Abdul ;
Paterson, Steve ;
Mowat, Eilidh ;
Fothergill, Joanne L. ;
Walshaw, Martin J. ;
Winstanley, Craig .
JOURNAL OF CYSTIC FIBROSIS, 2013, 12 (06) :790-793
[4]   Impact of the CFTR-Potentiator Ivacaftor on Airway Microbiota in Cystic Fibrosis Patients Carrying A G551D Mutation [J].
Bernarde, Cedric ;
Keravec, Marlene ;
Mounier, Jerome ;
Gouriou, Stephanie ;
Rault, Gilles ;
Ferec, Claude ;
Barbier, Georges ;
Hery-Arnaud, Genevieve .
PLOS ONE, 2015, 10 (04)
[5]   Computed tomography correlates with pulmonary exacerbations in children with cystic fibrosis [J].
Brody, AS ;
Sucharew, H ;
Campbell, JD ;
Millard, SP ;
Molina, PL ;
Klein, JS ;
Quan, J .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 172 (09) :1128-1132
[6]   Recombination is a key driver of genomic and phenotypic diversity in a Pseudomonas aeruginosa population during cystic fibrosis infection [J].
Darch, Sophie E. ;
McNally, Alan ;
Harrison, Freya ;
Corander, Jukka ;
Barr, Helen L. ;
Paszkiewicz, Konrad ;
Holden, Stephen ;
Fogarty, Andrew ;
Crusz, Shanika A. ;
Diggle, Stephen P. .
SCIENTIFIC REPORTS, 2015, 5
[7]  
EVALDSON G, 1982, SCAND J INFECT DIS, P9
[8]   Pathophysiology and management of pulmonary infections in cystic fibrosis [J].
Gibson, RL ;
Burns, JL ;
Ramsey, BW .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (08) :918-951
[9]   Pseudomonas aeruginosa in Cystic Fibrosis Patients With G551D-CFTR Treated With Ivacaftor [J].
Heltshe, Sonya L. ;
Mayer-Hamblett, Nicole ;
Burns, Jane L. ;
Khan, Umer ;
Baines, Arthur ;
Ramsey, Bonnie W. ;
Rowe, Steven M. .
CLINICAL INFECTIOUS DISEASES, 2015, 60 (05) :703-712
[10]  
Hisert KB, 2016, PEDIATR PULM, V51, P299