Evidence map›Paper›PMID 40671830›Full record

ReviewJHEP reports : innovation in hepatology2025

Regulatory T cell therapy in autoimmune liver disease and transplantation.

Maegen Fleming, Alberto Sanchez-Fueyo, Niloufar Safinia

Abstract readReview
In one paragraph

Review in JHEP reports : innovation in hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

3 authors.

Maegen FlemingRoger Williams Institute of Liver Studies, Department of Inflammation Biology, School of Immunology and Microbial Sciences, James Black Centre, King's College London, London, SE5 9NU, United Kingdom.
Alberto Sanchez-FueyoRoger Williams Institute of Liver Studies, Department of Inflammation Biology, School of Immunology and Microbial Sciences, James Black Centre, King's College London, London, SE5 9NU, United Kingdom.
Niloufar SafiniaRoger Williams Institute of Liver Studies, Department of Inflammation Biology, School of Immunology and Microbial Sciences, James Black Centre, King's College London, London, SE5 9NU, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this review, we explore the application of regulatory T cells (Tregs) as cellular therapies in the setting of autoimmune liver diseases and liver transplantation. At present, there are limited treatment options for end-stage liver disease, which in many cases requires transplantation. Following liver transplantation, immunosuppressive drugs are administered, often throughout the course of the patient's life, to prevent organ rejection. When used for a prolonged period, immunosuppressive drugs can have detrimental effects on the patient's health and quality of life. Tregs are an attractive target for cellular therapy in this context because of their innate ability to control inflammatory immune responses. In this review, we cover the different generations of Treg-based therapies, their potential roles in the treatment of autoimmune liver diseases and transplantation, and the future outlook for Tregs as cellular therapies.

Indexed as

Adoptive cell therapyAntigen specific TregsAutoimmune liver disease (AILD)Chimeric antigen receptor (CAR)Clinical TrialsIn vivo modulationLiver transplantationLow-dose IL-2Regulatory T cells (Tregs)

Identifiers

PMID40671830
PMCPMC12266500

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.