Evidence map›Paper›PMID 36688525›Full record

ArticleeLife2023

Compartmentalization and persistence of dominant (regulatory) T cell clones indicates antigen skewing in juvenile idiopathic arthritis.

Gerdien Mijnheer, Nila Hendrika Servaas, Jing Yao Leong, Arjan Boltjes, Eric Spierings, Phyllis Chen, Liyun Lai, Alessandra Petrelli, Sebastiaan Vastert, Rob J de Boer and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The 'TNature reviews. Rheumatology · 2025
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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

13 authors at 2 institutions in 2 countries.

Gerdien Mijnheer *Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Nila Hendrika Servaas *Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.ORCID 0000-0002-9825-7554
Jing Yao LeongTranslational Immunology Institute, Singhealth/Duke-NUS Academic Medical Centre, the Academia, Singapore, Singapore.
Arjan BoltjesCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Eric SpieringsCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.ORCID 0000-0001-9441-1019
Phyllis ChenTranslational Immunology Institute, Singhealth/Duke-NUS Academic Medical Centre, the Academia, Singapore, Singapore.
Liyun LaiTranslational Immunology Institute, Singhealth/Duke-NUS Academic Medical Centre, the Academia, Singapore, Singapore.
Alessandra PetrelliCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Sebastiaan VastertCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Rob J de BoerTheoretical Biology, Utrecht University, Utrecht, Netherlands.ORCID 0000-0002-2130-691X
Salvatore AlbaniTranslational Immunology Institute, Singhealth/Duke-NUS Academic Medical Centre, the Academia, Singapore, Singapore.
Aridaman Pandit *Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.ORCID 0000-0003-2057-9737
Femke van Wijk *Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.ORCID 0000-0001-8343-1356
Utrecht University · NLSingHealth Duke-NUS Academic Medical Centre · SG

Funding

ZonMw 91714332
6 · The paper itself

Abstract

Autoimmune inflammation is characterized by tissue infiltration and expansion of antigen-specific T cells. Although this inflammation is often limited to specific target tissues, it remains yet to be explored whether distinct affected sites are infiltrated with the same, persistent T cell clones. Here, we performed CyTOF analysis and T cell receptor (TCR) sequencing to study immune cell composition and (hyper-)expansion of circulating and joint-derived Tregs and non-Tregs in juvenile idiopathic arthritis (JIA). We studied different joints affected at the same time, as well as over the course of relapsing-remitting disease. We found that the composition and functional characteristics of immune infiltrates are strikingly similar between joints within one patient, and observed a strong overlap between dominant T cell clones, especially Treg, of which some could also be detected in circulation and persisted over the course of relapsing-remitting disease. Moreover, these T cell clones were characterized by a high degree of sequence similarity, indicating the presence of TCR clusters responding to the same antigens. These data suggest that in localized autoimmune disease, there is autoantigen-driven expansion of both Teffector and Treg clones that are highly persistent and are (re)circulating. These dominant clones might represent interesting therapeutic targets.

Indexed as

Arthritis, JuvenileClone CellsHumansInflammationReceptors, Antigen, T-CellT-Lymphocytes, RegulatoryReceptors, Antigen, T-CellCyTOFhumanimmunologyinflammationjuvenile idiopathic arthritisregulatory T cellt cell receptortissue inflammation

Identifiers

PMID36688525
PMCPMC9995115
OpenAlexW4317749668

What OpenQuestion 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 OpenQuestion graph.