Evidence map›Paper›PMID 35090380›Full record

ArticleGut microbes

AhR/IL-22 pathway as new target for the treatment of post-infectious irritable bowel syndrome symptoms.

Maëva Meynier, Elodie Baudu, Nathalie Rolhion, Manon Defaye, Marjolène Straube, Valentine Daugey, Morgane Modoux, Ivan Wawrzyniak, Frédéric Delbac, Roamin Villéger and 12 more

Open access · goldAbstract 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 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

48 citing papers in PubMed, 77 citations in OpenAlex.

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  9. EngineeredAnimal nutrition (Zhongguo xu mu shou yi xue hui) · 2026
    Article
  10. Frontiers in microbiology · 2026
    Review
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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

22 authors at 4 institutions in 3 countries.

Maëva MeynierM2iSH, UMR 1071 INSERM, University of Clermont Auvergne, INRAE USC 2018, Clermont-Ferrand 63001, France.
Elodie BauduM2iSH, UMR 1071 INSERM, University of Clermont Auvergne, INRAE USC 2018, Clermont-Ferrand 63001, France.
Nathalie RolhionSorbonne University, INSERM, Centre de Recherche Saint-Antoine, CRSA, AP-HP, Saint Antoine Hospital, Gastroenterology Department, F-75012 Paris, France.
Manon DefayeNeuroDol, UMR 1107 INSERM, University of Clermont Auvergne, Clermont-Ferrand 63001, France.
Marjolène StraubeSorbonne University, INSERM, Centre de Recherche Saint-Antoine, CRSA, AP-HP, Saint Antoine Hospital, Gastroenterology Department, F-75012 Paris, France.
Valentine DaugeyNeuroDol, UMR 1107 INSERM, University of Clermont Auvergne, Clermont-Ferrand 63001, France.
Morgane ModouxSorbonne University, INSERM, Centre de Recherche Saint-Antoine, CRSA, AP-HP, Saint Antoine Hospital, Gastroenterology Department, F-75012 Paris, France.
Ivan WawrzyniakLMGE, CNRS 6023, University of Clermont Auvergne, Clermont-Ferrand 63001, France.
Frédéric DelbacLMGE, CNRS 6023, University of Clermont Auvergne, Clermont-Ferrand 63001, France.
Roamin VillégerM2iSH, UMR 1071 INSERM, University of Clermont Auvergne, INRAE USC 2018, Clermont-Ferrand 63001, France.
Mathieu MéleineNeuroDol, UMR 1107 INSERM, University of Clermont Auvergne, Clermont-Ferrand 63001, France.
Esther Borras NoguesUniversité Paris-Saclay, Institut National de la Recherche Agronomique et Environnementale (INRAE), AgroParisTech UMR 1319 MICALIS, Jouy-en-Josas, France.
Catherine GodfraindM2iSH, UMR 1071 INSERM, University of Clermont Auvergne, INRAE USC 2018, Clermont-Ferrand 63001, France.
Nicolas BarnichM2iSH, UMR 1071 INSERM, University of Clermont Auvergne, INRAE USC 2018, Clermont-Ferrand 63001, France.
Denis ArdidNeuroDol, UMR 1107 INSERM, University of Clermont Auvergne, Clermont-Ferrand 63001, France.
Philippe PoirierM2iSH, UMR 1071 INSERM, University of Clermont Auvergne, INRAE USC 2018, Clermont-Ferrand 63001, France.
Harry SokolSorbonne University, INSERM, Centre de Recherche Saint-Antoine, CRSA, AP-HP, Saint Antoine Hospital, Gastroenterology Department, F-75012 Paris, France.ORCID 0000-0002-2914-1822
Jean-Marc ChatelUniversité Paris-Saclay, Institut National de la Recherche Agronomique et Environnementale (INRAE), AgroParisTech UMR 1319 MICALIS, Jouy-en-Josas, France.
Philippe LangellaUniversité Paris-Saclay, Institut National de la Recherche Agronomique et Environnementale (INRAE), AgroParisTech UMR 1319 MICALIS, Jouy-en-Josas, France.
Valérie LivrelliM2iSH, UMR 1071 INSERM, University of Clermont Auvergne, INRAE USC 2018, Clermont-Ferrand 63001, France.
Mathilde BonnetM2iSH, UMR 1071 INSERM, University of Clermont Auvergne, INRAE USC 2018, Clermont-Ferrand 63001, France.ORCID 0000-0003-3629-7267
Frédéric Antonio CarvalhoNeuroDol, UMR 1107 INSERM, University of Clermont Auvergne, Clermont-Ferrand 63001, France.ORCID 0000-0003-1592-2369
Inserm · FRAgroParisTech · FRCentre National de la Recherche Scientifique · FRMicrobe, Intestine, Inflammation and Host Susceptibility · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alterations in brain/gut/microbiota axis are linked to Irritable Bowel Syndrome (IBS) physiopathology. Upon gastrointestinal infection, chronic abdominal pain and anxio-depressive comorbidities may persist despite pathogen clearance leading to Post-Infectious IBS (PI-IBS). This study assesses the influence of tryptophan metabolism, and particularly the microbiota-induced AhR expression, on intestinal homeostasis disturbance following gastroenteritis resolution, and evaluates the efficacy of IL-22 cytokine vectorization on PI-IBS symptoms. The

Indexed as

AnimalsBacteriaCognitionDepressionFatty Acids, VolatileGastrointestinal MicrobiomeHumansInterleukin-22InterleukinsIntestinesIrritable Bowel SyndromeMiceMice, Inbred C57BLReceptors, Aryl HydrocarbonFatty Acids, VolatileInterleukin-22InterleukinsReceptors, Aryl Hydrocarbonahrcitrobacter rodentiumcolonic-associated microbiotail-22lactococcus lactisPost-infectious ibstryptophanwell-being disorders

Identifiers

PMID35090380
PMCPMC8803069
OpenAlexW4210789669

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.