Evidence map›Paper›PMID 42211685›Full record

ArticleDiscovery immunology2026

A pathogenic CD4 T cell phenotype in experimental uveitis shares common features with other immune mediated inflammatory diseases.

Amy Ward, Oliver H Bell, Luis Martinez-Robles, Phillipa J P Lait, Colin J Chu, David A Copland, Andrew D Dick, Lindsay B Nicholson

Abstract read
In one paragraph

Article in Discovery immunology, 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

8 authors.

Amy WardSchool of Cellular and Molecular Medicine, Faculty of Life Sciences, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-4731-3333
Oliver H BellAcademic Unit of Ophthalmology, Translational Health Sciences, University of Bristol, Bristol, UK.
Luis Martinez-RoblesSchool of Cellular and Molecular Medicine, Faculty of Life Sciences, University of Bristol, Bristol, UK.
Phillipa J P LaitAcademic Unit of Ophthalmology, Translational Health Sciences, University of Bristol, Bristol, UK.
Colin J ChuAcademic Unit of Ophthalmology, Translational Health Sciences, University of Bristol, Bristol, UK.
David A CoplandAcademic Unit of Ophthalmology, Translational Health Sciences, University of Bristol, Bristol, UK.
Andrew D DickSchool of Cellular and Molecular Medicine, Faculty of Life Sciences, University of Bristol, Bristol, UK.
Lindsay B NicholsonSchool of Cellular and Molecular Medicine, Faculty of Life Sciences, University of Bristol, Bristol, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Murine ocular autoimmunity develops through three stages; prodrome, primary peak, and secondary regulation. During the prodromal phase, leukocytes accumulate within the retina and vitreous. Methods: Using the adoptive transfer of ocular antigen reactive T cells to induce experimental autoimmune uveitis, we can analyse the disease course and track the transferred cells being recruited to the ocular environment from prodrome through peak of disease to secondary regulation. Results: During initiation (the prodrome) of disease 'pathogenic' transferred CD4 Conclusion: Due to the persistence of the original transferred population throughout clinical disease, in depth analysis of this population could suggest pathways contributing to persistent ocular autoimmunity.

Indexed as

adoptive transferautoantigen specificautoreactiveCD4+ T cellEAUuveitis

Identifiers

PMID42211685
PMCPMC13213613

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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.