Evidence map›Paper›PMID 33526927›Full record

ReviewNature reviews. Rheumatology2021

Location, location, location: how the tissue microenvironment affects inflammation in RA.

Christopher D Buckley, Caroline Ospelt, Steffen Gay, Kim S Midwood

Erratum issuedOpen access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Rheumatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
18.7field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 152 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
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  11. Biocatalytic Nanoregulators Restore Joint Redox-Immune Homeostasis in Rheumatoid Arthritis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
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  20. Review

14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 3 countries.

Christopher D BuckleyKennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Caroline OspeltCentre of Experimental Rheumatology, Department of Rheumatology, University Hospital of Zurich, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-9151-4650
Steffen GayCentre of Experimental Rheumatology, Department of Rheumatology, University Hospital of Zurich, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-2920-9268
Kim S MidwoodKennedy Institute of Rheumatology, University of Oxford, Oxford, UK. kim.midwood@kennedy.ox.ac.uk.ORCID http://orcid.org/0000-0002-8813-2977
University of Zurich · CHQueen Elizabeth Hospital Birmingham · GBUniversity of Oxford · GB

Funding

Department of HealthMedical Research Council MR/S025308/1Medical Research Council MR/S035850/1Versus Arthritis 19791Versus Arthritis 20003Versus Arthritis 20298Versus Arthritis 22253Wellcome Trust
6 · The paper itself

Abstract

Current treatments for rheumatoid arthritis (RA) do not work well for a large proportion of patients, or at all in some individuals, and cannot cure or prevent this disease. One major obstacle to developing better drugs is a lack of complete understanding of how inflammatory joint disease arises and progresses. Emerging evidence indicates an important role for the tissue microenvironment in the pathogenesis of RA. Each tissue is made up of cells surrounded and supported by a unique extracellular matrix (ECM). These complex molecular networks define tissue architecture and provide environmental signals that programme site-specific cell behaviour. In the synovium, a main site of disease activity in RA, positional and disease stage-specific cellular diversity exist. Improved understanding of the architecture of the synovium from gross anatomy to the single-cell level, in parallel with evidence demonstrating how the synovial ECM is vital for synovial homeostasis and how dysregulated signals from the ECM promote chronic inflammation and tissue destruction in the RA joint, has opened up new ways of thinking about the pathogenesis of RA. These new ideas provide novel therapeutic approaches for patients with difficult-to-treat disease and could also be used in disease prevention.

Indexed as

Arthritis, RheumatoidCellular MicroenvironmentExtracellular MatrixFibroblastsHomeostasisHumansInflammationMacrophagesMolecular Targeted TherapySeverity of Illness IndexSynovial Membrane

Identifiers

PMID33526927
OpenAlexW3128437194

What OpenQuestion holds

Textmetadata
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.