Evidence map›Paper›PMID 30611306›Full record

ArticleArthritis research & therapy2019

Altered composition and phenotype of mucosal-associated invariant T cells in early untreated rheumatoid arthritis.

Hester Koppejan, Diahann T S L Jansen, Marjolijn Hameetman, Ranjeny Thomas, Rene E M Toes, Floris A van Gaalen

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

39 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Mucosal-Associated Invariant T Cells in Rheumatic Diseases.Arthritis & rheumatology (Hoboken, N.J.) · 2026
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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

6 authors at 2 institutions in 2 countries.

Hester KoppejanDepartment of Rheumatology, Leiden University Medical Center, PO Box 9600 (Zone C1-R), Albinusdreef 2, 2233 ZA, Leiden, the Netherlands. h.j.koppejan@lumc.nl.ORCID 0000-0002-6046-9113
Diahann T S L JansenDiamantina Institute, Translational Research Institute, University of Queensland, Woolloongabba, QLD, Australia.
Marjolijn HameetmanDepartment of Rheumatology, Leiden University Medical Center, PO Box 9600 (Zone C1-R), Albinusdreef 2, 2233 ZA, Leiden, the Netherlands.
Ranjeny ThomasDiamantina Institute, Translational Research Institute, University of Queensland, Woolloongabba, QLD, Australia.
Rene E M ToesDepartment of Rheumatology, Leiden University Medical Center, PO Box 9600 (Zone C1-R), Albinusdreef 2, 2233 ZA, Leiden, the Netherlands.
Floris A van GaalenDepartment of Rheumatology, Leiden University Medical Center, PO Box 9600 (Zone C1-R), Albinusdreef 2, 2233 ZA, Leiden, the Netherlands.
Leiden University Medical Center · NLTranslational Research Institute · AU

Funding

European Federation of Pharmaceutical Industries and Associations NAReumafonds 15-2-401Seventh Framework Programme FP7/2007-2013The Innovative Medicines Initiative Joint Undertaking 115142
6 · The paper itself

Abstract

backgroundMucosal-associated invariant T (MAIT) cells are innate-like T cells that recognise bacterial metabolites presented by MHC class I-related protein 1 (MR1). Bacterial dysbiosis has been implicated in auto-inflammatory disease development. We investigated MAIT cells in early, untreated rheumatoid arthritis (RA) and spondyloarthritis (SpA) patients.

methodsBlood and synovial fluid mononuclear cells obtained from patients (SpA/RA) and controls were stimulated with fixed Escherichia coli to provide MAIT ligand. Cells were analysed by flow cytometry and MAIT cells were identified by MR1-5-OP-RU tetramers. Synovial biopsies were studied by confocal microscopy.

resultsPeripheral and synovial CD3

conclusionIn early untreated RA patients, the peripheral MAIT cell composition was altered, with reduced levels of CD161 expression, and cells were hyporesponsive to stimulation. MAIT cell dysfunction may provide a link between the microbiome and development of RA.

Indexed as

PhenotypeArthritis, RheumatoidCohort StudiesFemaleHumansMaleMucosal-Associated Invariant T CellsSynovial FluidCD161Mucosal-associated invariant T cellsRheumatoid arthritisSpondyloarthritis

Identifiers

PMID30611306
PMCPMC6321723
OpenAlexW2907681427

What OpenQuestion holds

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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.