Evidence map›Paper›PMID 39244776›Full record

ArticleGut microbes

Inflammation promotes stomach epithelial defense by stimulating the secretion of antimicrobial peptides in the mucus.

Megi Vllahu, Antonia Voli, Valerio Licursi, Claudia Zagami, Antonella D'Amore, Jan Traulsen, Sara Woelffling, Monika Schmid, Robbie Crickley, Richard Lisle and 4 more

Abstract read
In one paragraph

Article in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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. Review
  2. Physical, chemical, and structural properties of human gastric organoid-derived mucus.American journal of physiology. Gastrointestinal and liver physiology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Post-burn Lung Inflammation Is Associated With Induction of Pulmonary Cathelicidin-related Antimicrobial Peptide and S100a8 in Mice.Journal of burn care & research : official publication of the American Burn Association · 2025
    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

14 authors.

Megi VllahuDepartment of Pharmacy, University of Salerno, Fisciano, Salerno, Italy.
Antonia VoliDepartment of Pharmacy, University of Salerno, Fisciano, Salerno, Italy.ORCID 0009-0000-2410-8081
Valerio LicursiInstitute of Molecular Biology and Pathology (IBPM), National Research Council (CNR) of Italy c/o Department of Biology and Biotechnology ''C. Darwin'', Sapienza University, Rome, Italy.ORCID 0000-0002-8172-1437
Claudia ZagamiLudwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.ORCID 0000-0001-5280-8261
Antonella D'AmoreLudwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.ORCID 0000-0002-3441-4397
Jan TraulsenLudwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.ORCID 0000-0001-9340-9232
Sara WoelfflingDepartment of Molecular Biology, Max Planck Institute for Infection Biology, Berlin, Germany.
Monika SchmidDepartment of Molecular Biology, Max Planck Institute for Infection Biology, Berlin, Germany.
Robbie CrickleyLudwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Richard LisleLudwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Alexander LinkDepartment of Gastroenterology, Hepatology and Infectious Diseases, Otto-von-Guericke University Hospital, Magdeburg, Germany.ORCID 0000-0002-9514-4562
Alessandra ToscoDepartment of Pharmacy, University of Salerno, Fisciano, Salerno, Italy.
Thomas F MeyerDepartment of Molecular Biology, Max Planck Institute for Infection Biology, Berlin, Germany.ORCID 0000-0002-6120-8679
Francesco BoccellatoDepartment of Molecular Biology, Max Planck Institute for Infection Biology, Berlin, Germany.ORCID 0000-0001-6013-7154

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mucus serves as a protective barrier in the gastrointestinal tract against microbial attacks. While its role extends beyond merely being a physical barrier, the extent of its active bactericidal properties remains unclear, and the mechanisms regulating these properties are not yet understood. We propose that inflammation induces epithelial cells to secrete antimicrobial peptides, transforming mucus into an active bactericidal agent. To investigate the properties of mucus, we previously developed mucosoid culture models that mimic the healthy human stomach epithelium. Similar to organoids, mucosoids are stem cell-driven cultures; however, the cells are cultivated on transwells at air-liquid interface. The epithelial cells of mucosoids form a polarized monolayer, allowing differentiation into all stomach lineages, including mucus-secreting cells. This setup facilitates the secretion and accumulation of mucus on the apical side of the mucosoids, enabling analysis of its bactericidal effects and protein composition, including antimicrobial peptides. Our findings show that TNFα, IL1β, and IFNγ induce the secretion of antimicrobials such as lactotransferrin, lipocalin2, complement component 3, and CXCL9 into the mucus. This antimicrobial-enriched mucus can partially eliminate

Indexed as

Antimicrobial PeptidesGastric MucosaHelicobacter pyloriInflammationMucusEpithelial CellsHelicobacter InfectionsHumansOrganoidsStomachAntimicrobial PeptidesAntimicrobial peptidesEpithelial defenceHelicobacter pyloriInflammationInnate immunityMucusStomach

Identifiers

PMID39244776
PMCPMC11382725

What OpenQuestion 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 OpenQuestion graph.