Evidence map›Paper›PMID 11709450›Full record

ArticleAnnals of the rheumatic diseases2001

Detection of immune deposits in skin lesions of patients with Wegener's granulomatosis.

R H Brons, M C de Jong, N K de Boer, C A Stegeman, C G Kallenberg, J W Tervaert

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Article in Annals of the rheumatic diseases, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Mechanisms of vascular damage in ANCA vasculitis.Seminars in immunopathology · 2022
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Pathogenesis of ANCA-associated vasculitis.Current rheumatology reports · 2012
    Review
  11. Review
  12. Article
  13. Article
  14. Pathogenesis of ANCA-associated vasculitis.Rheumatic diseases clinics of North America · 2010
    Review
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 3 institutions in 2 countries.

R H BronsDepartment of Clinical Immunology, University Hospital Groningen, Groningen, The Netherlands.
M C de Jong
N K de Boer
C A Stegeman
C G Kallenberg
J W Tervaert
Hanze University of Applied Sciences · NLKidney Centre · PKUniversity of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWegener's granulomatosis (WG) is considered a pauci-immune systemic vasculitis based on the absence of immune deposits in renal biopsies of patients with active disease. In animal models of antineutrophil cytoplasmic antibody (ANCA) associated glomerulonephritis, immune deposits along the glomerular capillary wall are present at early stages of lesion development. These deposits are degraded rapidly, resulting in "pauci-immune" lesions.

objectiveTo test the hypothesis that immune deposits can also be detected in early lesions of patients with WG, thereby initiating an inflammatory reaction that, in time, is augmented in the presence of ANCA, resulting in pauci-immune lesions later on.

methodsThe presence of immune deposits in skin biopsies taken within 48 hours of lesion development was investigated. Direct immunofluorescence was used to examine 32 skin biopsies for the presence of immune deposits (IgG, IgA, IgM, C3c). When possible, a comparison was made between the immunofluorescence findings in renal and skin biopsies taken at the same time.

resultsFour of 11 biopsies taken at initial presentation and four of 21 biopsies taken at the onset of a relapse of WG showed IgG and/or IgA containing immune deposits in the subepidermal blood vessels. All nine renal biopsies showed pauci-immune glomerulonephritis, irrespective of the presence (n=5) or absence (n=4) of immune deposits in the skin biopsy.

conclusionA substantial number of skin biopsies showed immune deposits during active disease. These results could support the hypothesis that immune complexes may trigger vasculitic lesions in WG.

Indexed as

AdultAgedAntigen-Antibody ComplexBiopsyComplement C3cFemaleFluorescent Antibody Technique, DirectGranulomatosis with PolyangiitisHumansImmunoglobulin AImmunoglobulin GKidneyMaleMiddle AgedRecurrenceSkinAntigen-Antibody ComplexComplement C3cImmunoglobulin AImmunoglobulin G

Identifiers

PMID11709450
PMCPMC1753448
OpenAlexW2108365772

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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.