Evidence map›Paper›PMID 42882476›Full record

ArticleCells2026

Differential Enteric Glial and Mast Cell Characteristics Distinguish Microscopic Colitis Subtypes Relative to Healthy and Disease Controls, with Treatment-Associated Reductions in Glial Reactivity and Mast Cell Degranulation in Collagenous Colitis.

Julie Beaudeau, Celia Escudero-Hernández, Vittorio Abruzzese, Georgios Katinios, Gustav Orell, Nawroz Barazanji, Susanna Walter, Henrik Hjortswang, Vytautas Kiudelis, Juozas Kupčinskas and 2 more

Abstract read
In one paragraph

Article in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Julie BeaudeauDepartment of Biomedical and Clinical Sciences, Linköping University, 58185 Linköping, Sweden.ORCID 0000-0002-3952-5926
Celia Escudero-HernándezInstitute of Clinical Molecular Biology, Christian-Albrechts-University and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.ORCID 0000-0001-8906-3101
Vittorio AbruzzeseDepartment of Biomedical and Clinical Sciences, Linköping University, 58185 Linköping, Sweden.
Georgios KatiniosDepartment of Gastroenterology and Hepatology, Linköping University Hospital, 58185 Linköping, Sweden.ORCID 0009-0001-5476-6082
Gustav OrellDepartment of Gastroenterology and Hepatology, Linköping University Hospital, 58185 Linköping, Sweden.ORCID 0009-0003-1447-9382
Nawroz BarazanjiDepartment of Gastroenterology and Hepatology, Linköping University Hospital, 58185 Linköping, Sweden.
Susanna WalterDepartment of Gastroenterology and Hepatology, Linköping University Hospital, 58185 Linköping, Sweden.ORCID 0000-0002-3463-9705
Henrik HjortswangDepartment of Gastroenterology and Hepatology, Linköping University Hospital, 58185 Linköping, Sweden.
Vytautas KiudelisDepartment of Gastroenterology, Institute for Digestive Research, Lithuanian University of Health Sciences, 50009 Kaunas, Lithuania.
Juozas KupčinskasDepartment of Gastroenterology, Institute for Digestive Research, Lithuanian University of Health Sciences, 50009 Kaunas, Lithuania.ORCID 0000-0002-8760-7416
Andreas MünchDepartment of Gastroenterology and Hepatology, Linköping University Hospital, 58185 Linköping, Sweden.
Åsa V KeitaDepartment of Biomedical and Clinical Sciences, Linköping University, 58185 Linköping, Sweden.ORCID 0000-0002-6820-0215

Funding

European Crohn's and Colitis Organisation PROP-2550Linköping UniversityMedical Infection and Inflammation Center-MIICResearch Council of Lithuania S-MIP-24-133Ruth and Richard Julin FoundationSpanish Ministry of Science, Innovation and Universities BG24/00107Stiftelsen Apotekare Hedbergs Fund for Medical Research
6 · The paper itself

Abstract

Microscopic colitis (MC) is an inflammatory bowel disease characterized by chronic watery diarrhea. Although barrier dysfunction and immune activation are implicated, underlying mechanisms remain unclear. The aim of this study was to characterize enteric glial cells (EGC) and mast cell distribution across MC subtypes, assess treatment effects, and explore EGC-related gene expression and barrier markers. Colonic biopsies from patients with active collagenous colitis (aCC), budesonide-refractory CC (rCC), and active lymphocytic colitis (LC) were compared to irritable bowel syndrome (IBS), ulcerative colitis (UC), and healthy controls (HC). A subset of CC patients was studied during active disease (aCC) and in clinical remission due to budesonide treatment (tCC). Immunofluorescence quantified EGC positive for glial fibrillary acidic protein (EGC

Indexed as

Cell DegranulationColitis, CollagenousColitis, MicroscopicMast CellsNeurogliaAdultBudesonideCase-Control StudiesFemaleHumansMaleMiddle AgedBudesonidebudesonidecollagenous colitisgastrointestinal pathophysiologyimmune cellsimmune regulationimmunofluorescenceinflammationlymphocytic colitisrefractory colitisRNA-sequencingtight junctions

Identifiers

PMID42882476
PMCPMC13664090

What OpenQuestion holds

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Registered trials

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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.