Evidence map›Paper›PMID 15743476›Full record

ArticleArthritis research & therapy2005

The role of regulatory T cells in antigen-induced arthritis: aggravation of arthritis after depletion and amelioration after transfer of CD4+CD25+ T cells.

Oliver Frey, Peter K Petrow, Mieczyslaw Gajda, Kerstin Siegmund, Jochen Huehn, Alexander Scheffold, Alf Hamann, Andreas Radbruch, Rolf Bräuer

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

57 citing papers in PubMed, 125 citations in OpenAlex.

  1. Review
  2. The 'TNature reviews. Rheumatology · 2025
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  7. Angiotensin ATFrontiers in immunology · 2022
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  9. Characterization, biology, and expansion of regulatory T cells in the Cynomolgus macaque for preclinical studies.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2019
    Article
  10. Foxp3Frontiers in endocrinology · 2019
    Review
  11. Article
  12. Review
  13. Article
  14. High Interleukin-37 (IL-37) Expression and Increased Mucin-Domain Containing-3 (TIM-3) on Peripheral T Cells in Patients with Rheumatoid Arthritis.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  15. Annexin A1 and Autoimmunity: From Basic Science to Clinical Applications.International journal of molecular sciences · 2018
    Review
  16. Platforms for Single-Cell Collection and Analysis.International journal of molecular sciences · 2018
    Review
  17. Arthritis models: usefulness and interpretation.Seminars in immunopathology · 2017
    Review
  18. Article
  19. Article
  20. Article
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

9 authors at 4 institutions in 1 country.

Oliver FreyInstitut fur Pathologie, Friedrich-Schiller-Universität, Jena, Germany. oliver.frey@med.uni-jena.de
Peter K Petrow
Mieczyslaw Gajda
Kerstin Siegmund
Jochen Huehn
Alexander Scheffold
Alf Hamann
Andreas Radbruch
Rolf Bräuer
Friedrich Schiller University Jena · DEGerman Rheumatism Research Centre · DECharité - Universitätsmedizin Berlin · DEHumboldt-Universität zu Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is now generally accepted that CD4+CD25+ Treg cells play a major role in the prevention of autoimmunity and pathological immune responses. Their involvement in the pathogenesis of chronic arthritis is controversial, however, and so we examined their role in experimental antigen-induced arthritis in mice. Depletion of CD25-expressing cells in immunized animals before arthritis induction led to increased cellular and humoral immune responses to the inducing antigen (methylated bovine serum albumin; mBSA) and autoantigens, and to an exacerbation of arthritis, as indicated by clinical (knee joint swelling) and histological scores. Transfer of CD4+CD25+ cells into immunized mice at the time of induction of antigen-induced arthritis decreased the severity of disease but was not able to cure established arthritis. No significant changes in mBSA-specific immune responses were detected. In vivo migration studies showed a preferential accumulation of CD4+CD25+ cells in the inflamed joint as compared with CD4+CD25- cells. These data imply a significant role for CD4+CD25+ Treg cells in the control of chronic arthritis. However, transferred Treg cells appear to be unable to counteract established acute or chronic inflammation. This is of considerable importance for the timing of Treg cell transfer in potential therapeutic applications.

Indexed as

Immunotherapy, AdoptiveAnimalsArthritis, ExperimentalCD4-Positive T-LymphocytesChemotaxis, LeukocyteCytokinesDisease Models, AnimalFemaleHypersensitivity, DelayedLymphocyte DepletionMiceMice, Inbred C57BLReceptors, Interleukin-2Serum Albumin, BovineTh1 CellsTh2 CellsCytokinesmethylated bovine serum albuminReceptors, Interleukin-2Serum Albumin, Bovine

Identifiers

PMID15743476
PMCPMC1065322
OpenAlexW1555634619

What OpenQuestion holds

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LicenceCC BY
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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.