Evidence map›Paper›PMID 29258183›Full record

ReviewInternational journal of molecular sciences2017

The Lung Microbiome in Idiopathic Pulmonary Fibrosis: A Promising Approach for Targeted Therapies.

Aline Fastrès, Florence Felice, Elodie Roels, Catherine Moermans, Jean-Louis Corhay, Fabrice Bureau, Renaud Louis, Cécile Clercx, Julien Guiot

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Persistent microbial infections and idiopathic pulmonary fibrosis - an insight intoFrontiers in cellular and infection microbiology · 2024
    Review
  9. Article
  10. Article
  11. Sensitive cluster-free differential expression testing.bioRxiv : the preprint server for biology · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Microbiota and IPF: hidden and detected relationships.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2021
    Article
  17. Review
  18. Agonist-specific desensitization of PGENaunyn-Schmiedeberg's archives of pharmacology · 2020
    Article
  19. Article
  20. Review
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 1 institution in 1 country.

Aline FastrèsDepartment of Clinical Sciences, FARAH, Faculty of Veterinary Medicine, University of Liège, 4000 Liège, Belgium. afastres@uliege.be.ORCID 0000-0002-7327-3478
Florence FeliceRespiratory department, CHU Liège. Domaine universitaire du Sart Tilman, B35, 4000 Liège, Belgium. Florence.Felice@student.uliege.be.
Elodie RoelsDepartment of Clinical Sciences, FARAH, Faculty of Veterinary Medicine, University of Liège, 4000 Liège, Belgium. eroels@uliege.be.
Catherine MoermansRespiratory department, CHU Liège. Domaine universitaire du Sart Tilman, B35, 4000 Liège, Belgium. c.moermans@chu.ulg.ac.be.
Jean-Louis CorhayRespiratory department, CHU Liège. Domaine universitaire du Sart Tilman, B35, 4000 Liège, Belgium. jlcorhay@ulg.ac.be.
Fabrice BureauLaboratory of Cellular and Molecular Immunology, GIGA Research, University of Liège, 4000 Liège, Belgium. fabrice.bureau@uliege.be.
Renaud LouisRespiratory department, CHU Liège. Domaine universitaire du Sart Tilman, B35, 4000 Liège, Belgium. R.Louis@uliege.be.
Cécile ClercxDepartment of Clinical Sciences, FARAH, Faculty of Veterinary Medicine, University of Liège, 4000 Liège, Belgium. cclercx@uliege.be.
Julien GuiotRespiratory department, CHU Liège. Domaine universitaire du Sart Tilman, B35, 4000 Liège, Belgium. j.guiot@chu.ulg.ac.be.
University of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review focuses on the role of the lung microbiome in idiopathic pulmonary fibrosis. Although historically considered sterile, bacterial communities have now been well documented in lungs both in healthy and pathological conditions. Studies in idiopathic pulmonary fibrosis (IPF) suggest that increased bacterial burden and/or abundance of potentially pathogenic bacteria may drive disease progression, acute exacerbations, and mortality. More recent work has highlighted the interaction between the lung microbiome and the innate immune system in IPF, strengthening the argument for the role of both host and environment interaction in disease pathogenesis. Existing published data suggesting that the lung microbiome may represent a therapeutic target, via antibiotic administration, immunization against pathogenic organisms, or treatment directed at gastroesophageal reflux. Taken altogether, published literature suggests that the lung microbiome might serve in the future as a prognostic biomarker, a therapeutic target, and/or provide an explanation for disease pathogenesis in IPF.

Indexed as

Disease ProgressionHumansIdiopathic Pulmonary FibrosisLungLung Diseases, InterstitialMicrobiotaidiopathic pulmonary fibrosisinterstitial lung diseasesIPFmicrobiomemicrobiota

Identifiers

PMID29258183
PMCPMC5751336
OpenAlexW2781396506

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.