Evidence map›Paper›PMID 19381293›Full record

ArticlePloS one2009

CD45RC isoform expression identifies functionally distinct T cell subsets differentially distributed between healthy individuals and AAV patients.

Laurence Ordonez, Isabelle Bernard, Fatima-Ezzahra L'faqihi-Olive, Jan Willem Cohen Tervaert, Jan Damoiseaux, Abdelhadi Saoudi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. CD45RC Expression of Circulating CD8Journal of clinical medicine · 2019
    Article
  7. Observational
  8. Description of CD8Journal of immunology research · 2018
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. T cells in vascular inflammatory diseases.Frontiers in immunology · 2014
    Review
  14. Article
  15. Pathogenesis of ANCA-associated vasculitis.Current rheumatology reports · 2012
    Review
  16. Article
  17. Review
  18. Pathogenesis of ANCA-associated vasculitis.Rheumatic diseases clinics of North America · 2010
    Review
  19. Review
  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

6 authors at 4 institutions in 2 countries.

Laurence OrdonezInstitut National de la Santé et de la Recherche Médicale (INSERM) U563, Institut Fédératif de Recherche (IFR) 30, Hôpital Purpan and Université Paul Sabatier, Toulouse, France.
Isabelle Bernard
Fatima-Ezzahra L'faqihi-Olive
Jan Willem Cohen Tervaert
Jan Damoiseaux
Abdelhadi Saoudi
Maastricht University Medical Centre · NLUniversité Toulouse III - Paul Sabatier · FRHôpital Purpan · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In animal models of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), the proportion of CD45RC T cell subsets is important for disease susceptibility. Their human counterparts are, however, functionally ill defined. In this report, we studied their distribution in healthy controls (HC), AAV patients and in Systemic lupus erythematous (SLE) patients as disease controls. We showed that CD45RC expression level on human CD4 and CD8 T cells identifies subsets that are highly variable among individuals. Interestingly, AAV patients exhibit an increased proportion of CD45RC(low) CD4 T cells as compared to HC and SLE patients. This increase is stable over time and independent of AAV subtype, ANCA specificity, disease duration, or number of relapses. We also analyzed the cytokine profile of purified CD4 and CD8 CD45RC T cell subsets from HC, after stimulation with anti-CD3 and anti-CD28 mAbs. The CD45RC subsets exhibit different cytokine profiles. Type-1 cytokines (IL-2, IFN-gamma and TNF-alpha) were produced by all CD45RC T cell subsets, while the production of IL-17, type-2 (IL-4, IL-5) and regulatory (IL-10) cytokines was restricted to the CD45RC(low) subset. In conclusion, we have shown that CD45RC expression divides human T cells in functionally distinct subsets that are imbalanced in AAV. Since this imbalance is stable over time and independent of several disease parameters, we hypothesize that this is a pre-existing immune abnormality involved in the etiology of AAV.

Indexed as

T-Lymphocyte SubsetsAdultAgedCase-Control StudiesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCytokinesDependovirusFemaleFlow CytometryHumansLeukocyte Common AntigensMaleMiddle AgedParvoviridae InfectionsCytokinesLeukocyte Common Antigens

Identifiers

PMID19381293
PMCPMC2668071
OpenAlexW2063403608

What OpenQuestion holds

Textmetadata
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.