Evidence map›Paper›PMID 24018177›Full record

ArticleJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2014

Impact of azithromycin treatment on macrophage gene expression in subjects with cystic fibrosis.

Theodore J Cory, Susan E Birket, Brian S Murphy, Don Hayes, Michael I Anstead, Jamshed F Kanga, Robert J Kuhn, Heather M Bush, David J Feola

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The Effect of CFTR Modulators on Airway Infection in Cystic Fibrosis.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Observational
  9. Macrolides and viral infections: focus on azithromycin in COVID-19 pathology.International journal of antimicrobial agents · 2020
    Review
  10. Article
  11. A Flow Cytometric Method for Isolating Cystic Fibrosis Airway Macrophages from Expectorated Sputum.American journal of respiratory cell and molecular biology · 2019
    Article
  12. Transcriptional and functional diversity of human macrophage repolarization.The Journal of allergy and clinical immunology · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Role of IRE1α/XBP-1 in Cystic Fibrosis Airway Inflammation.International journal of molecular sciences · 2017
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Theodore J CoryDepartment of Pharmacy Practice and Science, University of Kentucky College of Pharmacy, 789 S. Limestone, Lexington, KY 40536, United States; Department of Pharmacy Practice, University of Nebraska College of Pharmacy, 986000 Nebraska Medical Center, Omaha, NE 68198, United States.
Susan E BirketDepartment of Pharmacy Practice and Science, University of Kentucky College of Pharmacy, 789 S. Limestone, Lexington, KY 40536, United States; Department of Medicine, University of Alabama at Birmingham, 1918 University Blvd., Birmingham, AL 35294, United States.
Brian S MurphyDepartment of Internal Medicine, University of Kentucky College of Medicine, 138 Leader Avenue, Lexington, KY 40506, United States.
Don HayesSection of Pulmonary Medicine, Department of Pediatrics, The Ohio State University, Nationwide Children's Hospital, 700 Children's Dr., Columbus, OH 43205, United States.
Michael I AnsteadDepartment of Pediatrics, University of Kentucky, 138 Leader Avenue, Lexington, KY 40506, United States.
Jamshed F KangaDepartment of Pediatrics, University of Kentucky, 138 Leader Avenue, Lexington, KY 40506, United States.
Robert J KuhnDepartment of Pharmacy Practice and Science, University of Kentucky College of Pharmacy, 789 S. Limestone, Lexington, KY 40536, United States.
Heather M BushDepartment of Biostatistics, University of Kentucky College of Medicine, 725 Rose Street, Lexington, KY 40536, United States.
David J FeolaDepartment of Pharmacy Practice and Science, University of Kentucky College of Pharmacy, 789 S. Limestone, Lexington, KY 40536, United States. Electronic address: david.feola@uky.edu.
University of Kentucky · USNationwide Children's Hospital · USNebraska Medical Center · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
Alternative macrophage activation in acute Pseudomonas pneumoniaR01AI095307 · NIAID · UNIVERSITY OF KENTUCKY · PI FEOLA, DAVID · 2012 to 2016
$1.8M
Kentucky Center for Clinical and Translational ScienceTL1TR000115 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$518k
Kentucky Center for Clinical and Translational ScienceTL1RR033172 · NCRR · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2011 to 2011
$161k
NCATS NIH HHS TL1 TR000115NCATS NIH HHS UL1 TR000117NCRR NIH HHS TL1 RR033172NIAID NIH HHS R01 AI095307
6 · The paper itself

Abstract

backgroundAzithromycin treatment improves clinical parameters in patients with CF, and alters macrophage activation from a pro-inflammatory (M1) phenotype to a pro-fibrotic, alternatively activated (M2) phenotype. The transcriptional profile of cells from patients receiving azithromycin is unknown.

methodsGene expression in association with macrophage polarization, inflammation, and tissue remodeling was assessed from sputum samples collected from patients with CF. Transcriptional profiles and clinical characteristics, including azithromycin therapy, were compared.

resultsExpression of NOS2 and TNFα was decreased in subjects receiving azithromycin, whereas expression of M2-associated genes was unaffected. Principal component analysis revealed gene expression profiles consistent with M1- (MMP9, NOS2, and TLR4) or M2-polarization (CCL18, fibronectin, and MR1) in select subject groups. These expression signatures did not significantly correlate with clinical characteristics.

conclusionsPro-inflammatory gene expression was low in subjects receiving AZM. Genes were stratified into groupings characteristic of M1- or M2-polarization, suggesting that overall polarization status is distinct among patient groups.

Indexed as

AzithromycinCystic FibrosisInflammationMacrophages, AlveolarAdultAnti-Bacterial AgentsChildFemaleGene ExpressionGene Expression ProfilingGenome-Wide Association StudyHumansInflammation MediatorsMacrophage ActivationMalePhenotypeAnti-Bacterial AgentsAzithromycinInflammation MediatorsReceptors, ImmunologicAzithromycinCystic fibrosisMacrophage phenotype

Identifiers

PMID24018177
PMCPMC4376357
OpenAlexW2027249720

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.