Evidence map›Paper›PMID 41704697›Full record

ArticleFrontiers in medicine2026

Voclosporin shows protective effect and intestinal barrier enforcement in experimental colitis.

M Gabel, A Knauss, Y Liu, M Mohamed Abdou, C Kaufmann, L Loges, M Stürzl, S Schürmann, M J Waldner, M F Neurath and 1 more

Abstract read
In one paragraph

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

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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

11 authors.

M Gabel *Department of Medicine 1, University Hospital Erlangen, Erlangen, Germany.
A Knauss *Department of Medicine 1, University Hospital Erlangen, Erlangen, Germany.
Y LiuDepartment of Medicine 1, University Hospital Erlangen, Erlangen, Germany.
M Mohamed AbdouDivision of Molecular and Experimental Surgery, Department of Surgery, Translational Research Center, Friedrich-Alexander University Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany.
C KaufmannDepartment of Medicine 1, University Hospital Erlangen, Erlangen, Germany.
L LogesDepartment of Medicine 1, University Hospital Erlangen, Erlangen, Germany.
M StürzlDivision of Molecular and Experimental Surgery, Department of Surgery, Translational Research Center, Friedrich-Alexander University Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany.
S SchürmannInstitute of Medical Biotechnology, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
M J WaldnerDepartment of Medicine 1, University Hospital Erlangen, Erlangen, Germany.
M F NeurathDepartment of Medicine 1, University Hospital Erlangen, Erlangen, Germany.
B WeigmannDepartment of Medicine 1, University Hospital Erlangen, Erlangen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment of inflammatory bowel disease (IBD) is still challenging. Therefore, it is crucial not only to develop new drugs specifically targeting IBD but also to evaluate the application and efficacy of already established pharmaceuticals used for related disorders. A promising new candidate is Voclosporin (Voc), a recently approved drug for lupus nephritis. In this study, we aimed to further elucidate the efficiency and the molecular mechanism of action of Voclosporin in comparison with its analogon cyclosporine A (CsA). Using an experimental colitis model and human PBMCs, we performed a comprehensive analysis including mini-endoscopy, histopathology, multi-photon endomicroscopy (MPEM), immunofluorescence staining, flow cytometry, and cytokine secretion profiling of murine lamina propria mononuclear cells (LPMCs). Treatment with Voc or CsA improved colitis-associated weight loss and reduced intestinal inflammation as assessed by endoscopy and histopathological stainings. Treatment with Voclosporin led to a significant increase of the barrier-strengthening protein claudin 3 in the colon of mice with experimentally induced colitis. Furthermore, treatment of stimulated human-derived PBMCs from healthy controls with Voclosporin and CsA inhibited the activation of IL2-inducible tyrosine kinase ITK, a known trigger of inflammation in IBD. These results further support the potential of Voclosporin as a promising therapeutic strategy for the treatment of acute intestinal inflammation.

Indexed as

calcineurin inhibitorexperimental colitisIBDtreatmentVoclosporin

Identifiers

PMID41704697
PMCPMC12908035

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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.