Literature DB >> 28222269

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

Katherine B Hisert1, Sonya L Heltshe2, Christopher Pope2, Peter Jorth3, Xia Wu4, Rachael M Edwards5, Matthew Radey6, Frank J Accurso7, Daniel J Wolter2, Gordon Cooke8, Ryan J Adam9, Suzanne Carter8, Brenda Grogan8, Janice L Launspach9, Seamas C Donnelly10, Charles G Gallagher8, James E Bruce4, David A Stoltz9, Michael J Welsh9, Lucas R Hoffman2,6, Edward F McKone8, Pradeep K Singh1,6.   

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.

Entities:  

Keywords:  Pseudomonas aeruginosa; cystic fibrosis; inflammation; ivacaftor

Mesh:

Substances:

Year:  2017        PMID: 28222269      PMCID: PMC5476912          DOI: 10.1164/rccm.201609-1954OC

Source DB:  PubMed          Journal:  Am J Respir Crit Care Med        ISSN: 1073-449X            Impact factor:   21.405


  23 in total

1.  Ivacaftor-Induced Proteomic Changes Suggest Monocyte Defects May Contribute to the Pathogenesis of Cystic Fibrosis.

Authors:  Katherine B Hisert; Kelly Q Schoenfelt; Gordon Cooke; Brenda Grogan; Jan L Launspach; Charles G Gallagher; Seamas C Donnelly; Michael J Welsh; Pradeep K Singh; Edward F McKone; Lev Becker
Journal:  Am J Respir Cell Mol Biol       Date:  2016-04       Impact factor: 6.914

2.  Antibacterial properties of the CFTR potentiator ivacaftor.

Authors:  Leah R Reznikov; Mahmoud H Abou Alaiwa; Cassie L Dohrn; Nick D Gansemer; Daniel J Diekema; David A Stoltz; Michael J Welsh
Journal:  J Cyst Fibros       Date:  2014-03-05       Impact factor: 5.482

Review 3.  The normal human anaerobic microflora.

Authors:  G Evaldson; A Heimdahl; L Kager; C E Nord
Journal:  Scand J Infect Dis Suppl       Date:  1982

4.  Random-effects models for longitudinal data.

Authors:  N M Laird; J H Ware
Journal:  Biometrics       Date:  1982-12       Impact factor: 2.571

5.  Pseudomonas aeruginosa in cystic fibrosis patients with G551D-CFTR treated with ivacaftor.

Authors:  Sonya L Heltshe; Nicole Mayer-Hamblett; Jane L Burns; Umer Khan; Arthur Baines; Bonnie W Ramsey; Steven M Rowe
Journal:  Clin Infect Dis       Date:  2014-11-25       Impact factor: 9.079

6.  Computed tomography correlates with pulmonary exacerbations in children with cystic fibrosis.

Authors:  Alan S Brody; Heidi Sucharew; Jonathan D Campbell; Steven P Millard; Paul L Molina; Jeffrey S Klein; Joanne Quan
Journal:  Am J Respir Crit Care Med       Date:  2005-08-11       Impact factor: 21.405

7.  Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation.

Authors:  Frank J Accurso; Steven M Rowe; J P Clancy; Michael P Boyle; Jordan M Dunitz; Peter R Durie; Scott D Sagel; Douglas B Hornick; Michael W Konstan; Scott H Donaldson; Richard B Moss; Joseph M Pilewski; Ronald C Rubenstein; Ahmet Z Uluer; Moira L Aitken; Steven D Freedman; Lynn M Rose; Nicole Mayer-Hamblett; Qunming Dong; Jiuhong Zha; Anne J Stone; Eric R Olson; Claudia L Ordoñez; Preston W Campbell; Melissa A Ashlock; Bonnie W Ramsey
Journal:  N Engl J Med       Date:  2010-11-18       Impact factor: 176.079

8.  BIGSdb: Scalable analysis of bacterial genome variation at the population level.

Authors:  Keith A Jolley; Martin C J Maiden
Journal:  BMC Bioinformatics       Date:  2010-12-10       Impact factor: 3.169

9.  Impact of the CFTR-potentiator ivacaftor on airway microbiota in cystic fibrosis patients carrying a G551D mutation.

Authors:  Cédric Bernarde; Marlène Keravec; Jérôme Mounier; Stéphanie Gouriou; Gilles Rault; Claude Férec; Georges Barbier; Geneviève Héry-Arnaud
Journal:  PLoS One       Date:  2015-04-08       Impact factor: 3.240

10.  Extensive diversification is a common feature of Pseudomonas aeruginosa populations during respiratory infections in cystic fibrosis.

Authors:  Abdul Ashish; Steve Paterson; Eilidh Mowat; Joanne L Fothergill; Martin J Walshaw; Craig Winstanley
Journal:  J Cyst Fibros       Date:  2013-05-01       Impact factor: 5.482

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  109 in total

1.  Answering the call to address cystic fibrosis treatment burden in the era of highly effective CFTR modulator therapy.

Authors:  Alex H Gifford; Nicole Mayer-Hamblett; Kelsie Pearson; David P Nichols
Journal:  J Cyst Fibros       Date:  2019-11-21       Impact factor: 5.482

Review 2.  Building global development strategies for cf therapeutics during a transitional cftr modulator era.

Authors:  N Mayer-Hamblett; S van Koningsbruggen-Rietschel; D P Nichols; D R VanDevanter; J C Davies; T Lee; A G Durmowicz; F Ratjen; M W Konstan; K Pearson; S C Bell; J P Clancy; J L Taylor-Cousar; K De Boeck; S H Donaldson; D G Downey; P A Flume; P Drevinek; C H Goss; I Fajac; A S Magaret; B S Quon; S M Singleton; J M VanDalfsen; G Z Retsch-Bogart
Journal:  J Cyst Fibros       Date:  2020-06-07       Impact factor: 5.482

3.  Losartan Rescues Inflammation-related Mucociliary Dysfunction in Relevant Models of Cystic Fibrosis.

Authors:  Michael D Kim; Nathalie Baumlin; Makoto Yoshida; Deepika Polineni; Sebastian F Salathe; Joseph K David; Charles A Peloquin; Adam Wanner; John S Dennis; Juliette Sailland; Philip Whitney; Frank T Horrigan; Juan R Sabater; William M Abraham; Matthias Salathe
Journal:  Am J Respir Crit Care Med       Date:  2020-02-01       Impact factor: 21.405

4.  Islet Hormone and Incretin Secretion in Cystic Fibrosis after Four Months of Ivacaftor Therapy.

Authors:  Andrea Kelly; Diva D De Leon; Saba Sheikh; Devaney Camburn; Christina Kubrak; Amy J Peleckis; Darko Stefanovski; Denis Hadjiliadis; Michael R Rickels; Ronald C Rubenstein
Journal:  Am J Respir Crit Care Med       Date:  2019-02-01       Impact factor: 21.405

5.  Lumacaftor (VX-809) restores the ability of CF macrophages to phagocytose and kill Pseudomonas aeruginosa.

Authors:  Roxanna Barnaby; Katja Koeppen; Amanda Nymon; Thomas H Hampton; Brent Berwin; Alix Ashare; Bruce A Stanton
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2017-11-16       Impact factor: 5.464

6.  Whole-blood transcriptomic responses to lumacaftor/ivacaftor therapy in cystic fibrosis.

Authors:  Benjamin T Kopp; James Fitch; Lisa Jaramillo; Chandra L Shrestha; Frank Robledo-Avila; Shuzhong Zhang; Sabrina Palacios; Fred Woodley; Don Hayes; Santiago Partida-Sanchez; Octavio Ramilo; Peter White; Asuncion Mejias
Journal:  J Cyst Fibros       Date:  2019-08-29       Impact factor: 5.482

Review 7.  Cystic Fibrosis Airway Microbiome: Overturning the Old, Opening the Way for the New.

Authors:  George A O'Toole
Journal:  J Bacteriol       Date:  2018-01-24       Impact factor: 3.490

Review 8.  Germline genetic variants with implications for disease risk and therapeutic outcomes.

Authors:  Amy L Pasternak; Kristen M Ward; Jasmine A Luzum; Vicki L Ellingrod; Daniel L Hertz
Journal:  Physiol Genomics       Date:  2017-09-08       Impact factor: 3.107

Review 9.  Ion Channel Modulators in Cystic Fibrosis.

Authors:  Martina Gentzsch; Marcus A Mall
Journal:  Chest       Date:  2018-05-08       Impact factor: 9.410

10.  The cystic fibrosis airway milieu enhances rescue of F508del in a pre-clinical model.

Authors:  Martina Gentzsch; Deborah M Cholon; Nancy L Quinney; Susan E Boyles; Mary E B Martino; Carla M P Ribeiro
Journal:  Eur Respir J       Date:  2018-12-20       Impact factor: 16.671

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