Evidence map›Paper›PMID 41950802›Full record

ReviewPharmacological reviews2026

Emerging mechanistic trends and clinical efficacy for methotrexate: Applications to inflammatory bowel disease.

Jeehyun Karen You, Theresa T Pizarro, Tommaso L Parigi

Abstract readReview
In one paragraph

Review in Pharmacological reviews, 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

3 authors.

Jeehyun Karen YouDepartments of Pathology and Biochemistry, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Theresa T PizarroDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio. Electronic address: theresa.pizarro@case.edu.
Tommaso L ParigiDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio; Università Vita-Salute and Department of Gastroenterology, IRCCS Ospedale San Raffaele, Milan, Italy.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
Molecular mechanisms of gasdermin recognition by proteases and autophagy proteins in cytokine releaseP01AI141350 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI DUBYAK, GEORGE R · 2020 to 2024
$9.4M
Combined Training Program in Digestive Disease SciencesT32DK083251 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI COMINELLI, FABIO, FIOCCHI, CLAUDIO · 2010 to 2025
$3.6M
The pathogenic roles of GSDMD-dependent gut epithelium extracellular vesicles in IBDR01DK125293 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI Theresa Torres Pizarro · 2021 to 2026
$3.3M
NIAID NIH HHS P01 AI141350NIDDK NIH HHS R01 DK125293NIDDK NIH HHS T32 DK083251NIGMS NIH HHS T32 GM007250
6 · The paper itself

Abstract

Methotrexate (MTX) was among the first steroid-sparing agents introduced for the treatment of inflammatory bowel disease (IBD). Its efficacy is well established for Crohn's disease, though studies of its use in ulcerative colitis have largely reported negative results, with only some, although inconsistent, findings suggesting limited benefit. In this review, we provide a comprehensive and up-to-date evaluation of MTX's use in IBD, including its key mechanisms of action(s), therapeutic value, as well as emerging targets that underscore the complexity of this drug and the biological landscape it alters. Despite its longstanding use, the full spectrum of MTX's effects contributing to its efficacy in IBD remains incompletely understood. Although multiple pathways have been implicated, the relative importance of each remains nebulous, and additional, unidentified functions may play a role, particularly in contexts not pertaining to immunomodulation. We highlight recent findings that poise MTX as an unexpected but promising agent for mucosal healing. We also provide a detailed evaluation of clinical studies, encompassing randomized controlled trials and observational data, highlighting MTX's effectiveness, differences in route of administration, safety profile, and limitations as they pertain to the management of IBD. As therapeutic targets for IBD evolve, we discuss MTX's future positioning by exploring clinical perspectives regarding its utility and examine the latest evidence that indicates there may be novel, previously unexplored, therapeutic potential. By bridging mechanistic insights with clinical evidence, this review underscores MTX's enduring, albeit niche, position in IBD therapy and highlights key areas for future investigation to optimize its use. SIGNIFICANCE STATEMENT: Methotrexate remains a valuable, though underutilized, therapeutic option for the management of inflammatory bowel disease. This review provides a comprehensive overview of methotrexate's pharmacology, integrating emerging mechanistic insights and clinical data to reframe its role beyond immunomodulation, particularly at the gastrointestinal mucosal interface, thereby identifying novel avenues for future research that may expand its clinical utility in inflammatory bowel disease.

Indexed as

Immunosuppressive AgentsInflammatory Bowel DiseasesMethotrexateAnimalsHumansTreatment OutcomeImmunosuppressive AgentsMethotrexate

Identifiers

PMID41950802
PMCPMC13197917

What Socratic holds

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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 Socratic graph.