Evidence map›Paper›PMID 42674109›Full record

ReviewCellular and molecular gastroenterology and hepatology2026

Mapping the Impact of Janus Kinase Inhibitors at a Cellular Resolution in Inflammatory Bowel Disease.

Jonas Louwers, Evelien Floor, Femke van Wijk, Yvonne Vercoulen, Bas Oldenburg

Abstract readReview
In one paragraph

Review in Cellular and molecular gastroenterology and hepatology, 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

5 authors.

Jonas LouwersDepartment of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands; Center for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Evelien FloorDepartment of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Femke van WijkCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
Yvonne VercoulenCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Bas OldenburgDepartment of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands. Electronic address: boldenbu@umcutrecht.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The advent of biologics and targeted oral small molecules has transformed the management of patients with inflammatory bowel disease (IBD), leading to increased rates of mucosal healing, fewer hospital admissions, and reduced need for surgery. In contrast to biologics that specifically target a receptor or its substrate, Janus kinase inhibitors (JAKis) interfere with several shared signaling pathways and therefore exert broader effects. Janus kinase-signal transducer and activator of transcription signaling (JAK-STAT) occupies a central position in multiple pro-inflammatory pathways and plays a pivotal role in the pathophysiology of autoimmune and inflammatory diseases. However, the pleiotropic effects of JAKis have greatly complicated the identification of cellular mediators of beneficial, adverse, or off-target effects, and this remains a challenge to date. This review summarizes current knowledge on the mechanisms of action of JAKis for the treatment of IBD, outlined by major cell types implicated in the pathophysiology of the disease. A deeper understanding of their effects on the diverse mucosal cell types is crucial to elucidate therapeutic mechanisms and explain treatment nonresponse.

Indexed as

Cytokine SignalingInflammatory Bowel DiseaseIntestinal Epithelial CellsJAK-STAT SignalingMacrophagesMonocytesMucosal ImmunologyT CellsTofacitinib

Identifiers

PMID42674109
PMCPMC13683868

What OpenQuestion holds

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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.