Evidence map›Paper›PMID 40581887›Full record

ArticleGut microbes2025

Intestinal host-microbe interactions fuel pulmonary inflammation in cigarette smoke exposed mice.

Sune K Yang-Jensen, Nora Näegele, Si Brask Sonne, Louis Koeninger, Marie Pineault, Félix Tremblay, Nanna Ny Kristensen, Lene Bay, Sophie Aubin, Mathieu C Morissette and 1 more

Abstract read
In one paragraph

Article in Gut microbes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Observational
  7. Review
  8. 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

11 authors.

Sune K Yang-JensenDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-8157-6516
Nora NäegeleDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Si Brask SonneDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-3194-3805
Louis KoeningerDepartment of Human Health, Novonesis A/S, Lyngby, Denmark.ORCID 0000-0001-9868-0670
Marie PineaultDepartment of Medicine, Quebec Heart and Lung Institute, Université Laval, Quebec, Canada.
Félix TremblayDepartment of Medicine, Quebec Heart and Lung Institute, Université Laval, Quebec, Canada.
Nanna Ny KristensenDepartment of Human Health, Novonesis A/S, Lyngby, Denmark.
Lene BayCosterton Biofilm Center, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Sophie AubinDepartment of Medicine, Quebec Heart and Lung Institute, Université Laval, Quebec, Canada.
Mathieu C MorissetteDepartment of Medicine, Quebec Heart and Lung Institute, Université Laval, Quebec, Canada.
Benjamin A H JensenDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0001-6991-0828

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiota has been implicated in numerous aspects of host health and immune regulation. Specifically, recent studies have linked gut microbes to the pathogenesis of chronic obstructive pulmonary disease (COPD), primarily induced by excessive cigarette smoke, although the underlying mechanisms remain elusive. Here, we investigated the role of gastrointestinal (GI) host-microbe interactions on pulmonary health. Using two distinct means of modulating GI host-microbe relations, we dissected how gut microbes fuel pulmonary inflammation in mouse models of cigarette smoke (CS)-induced lung disease. We found that CS caused profound changes to the colonic mucosa, with reduced mucus and increased bacterial encroachment. Modulating host-microbe interactions using antibiotics and recombinant human β-defensin 2 restricted colonic bacterial encroachment, limiting interactions between host and microbe. These strategies resulted in substantial ~50% decrease in pulmonary neutrophil infiltration following both acute and chronic exposure to CS. The reported findings provide additional evidence of a gut-lung axis, offering novel insight into the role of the gut microbiota in pulmonary immune activation, which could represent a novel avenue for future therapeutic strategies.

Indexed as

Gastrointestinal MicrobiomeHost Microbial InteractionsPneumoniaSmokeSmokingAnimalsBacteriabeta-DefensinsColonDisease Models, AnimalHumansIntestinal MucosaLungMaleMiceMice, Inbred C57BLbeta-DefensinsSmokebacterial encroachmentcigarette smokeCOPDgutgut–lung axislungMicrobiotamucus

Identifiers

PMID40581887
PMCPMC12218480

What Socratic holds

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LicenceCC BY
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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 Socratic graph.