Evidence map›Paper›PMID 12780698›Full record

ArticleClinical and experimental immunology2003

Staphylococcal superantigens and T cell expansions in Wegener's granulomatosis.

E R Popa, C A Stegeman, N A Bos, C G M Kallenberg, J W Cohen Tervaert

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Gut microbiome and kidney disease: a bidirectional relationship.Pediatric nephrology (Berlin, Germany) · 2017
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  9. Article
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  11. The immunopathology of ANCA-associated vasculitis.Seminars in immunopathology · 2014
    Review
  12. Article
  13. Review
  14. Pathogenesis of ANCA-associated vasculitis.Current rheumatology reports · 2012
    Review
  15. Article
  16. Pathogenesis of ANCA-associated vasculitis, an update.Clinical reviews in allergy & immunology · 2011
    Review
  17. Pathogenesis of ANCA-associated vasculitis.Rheumatic diseases clinics of North America · 2010
    Review
  18. Article
  19. Infection and vasculitis.Rheumatology (Oxford, England) · 2009
    Review
  20. 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

5 authors at 2 institutions in 1 country.

E R PopaDepartment of Clinical Immunology, University Hospital, Groningen, The Netherlands. e.popa@med.rug.nl
C A Stegeman
N A Bos
C G M Kallenberg
J W Cohen Tervaert
University of Groningen · NLDialyse Centrum Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In Wegener's granulomatosis (WG), a form of autoimmune systemic vasculitis, chronic carriage of Staphylococcus aureus constitutes a risk factor for the development of exacerbations. Circulating T cells in this disease are persistently activated, suggesting the presence of a chronic stimulus. A causal link between chronic carriage of S. aureus and chronic T cell activation in WG is conceivable, because S. aureus produces superantigens (SAg), which are potent T cell stimulators. Superantigenic stimulation of T cells results in expansion of T cell subsets expressing SAg-binding T cell receptor V-beta (Vbeta) chains. In the present study we hypothesized that in WG the presence of staphylococcal SAg is accompanied by expansion of SAg-reacting T cell subsets. We tested our hypothesis in a cross-sectional and a longitudinal study in which the association between seven staphylococcal SAg genes [typed by poplymerase chain reaction (PCR)], eight SAg-binding Vbeta chains and four SAg-non-binding Vbeta chains (assessed by flow-cytometry) was assessed. Both studies showed that T cell expansions were present at a significantly higher rate in WG patients than in healthy individuals, but were not associated with the presence of either S. aureus or its SAg. Moreover, T cell expansions were generally of small extent, and did not appear simultaneously in both CD4 and CD8 subsets. We conclude that in WG S. aureus effects its supposed pathogenic function by a mechanism other than superantigenic T cell activation.

Indexed as

AdultAgedAged, 80 and overCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCross-Sectional StudiesDNA, BacterialFemaleGranulomatosis with PolyangiitisHumansLongitudinal StudiesLymphocyte ActivationMaleMiddle AgedProspective StudiesReceptors, Antigen, T-Cell, alpha-betaDNA, BacterialReceptors, Antigen, T-Cell, alpha-betaSuperantigens

Identifiers

PMID12780698
PMCPMC1808727
OpenAlexW2061293215

What OpenQuestion holds

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Read underepoch 390

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.