Evidence map›Paper›PMID 25766482›Full record

ArticleClinical and experimental immunology2015

CD14 expression is increased on monocytes in patients with anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis and correlates with the expression of ANCA autoantigens.

R M Tarzi, J Liu, S Schneiter, N R Hill, T H Page, H T Cook, C D Pusey, K J Woollard

Open access · bronzeAbstract read
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Article in Clinical and experimental immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Mechanisms of vascular damage in ANCA vasculitis.Seminars in immunopathology · 2022
    Review
  9. Article
  10. CX3CL1-induced CD16Frontiers in immunology · 2022
    Article
  11. Article
  12. Immunopathogenesis of ANCA-Associated Vasculitis.International journal of molecular sciences · 2020
    Review
  13. Review
  14. Article
  15. 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

8 authors at 1 institution in 1 country.

R M TarziRenal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.
J LiuRenal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.
S SchneiterRenal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.
N R HillRenal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.
T H PageRenal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.
H T CookRenal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.
C D PuseyRenal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.
K J WoollardRenal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.
Imperial College London · GB

Funding

Versus Arthritis 18235
6 · The paper itself

Abstract

Monocyte subsets with differing functional properties have been defined by their expression of CD14 and CD16. We investigated these subsets in anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV) and determined their surface expression of ANCA autoantigens. Flow cytometry was performed on blood from 14 patients with active AAV, 46 patients with AAV in remission and 21 controls. The proportion of classical (CD14(high) CD16(neg/low)), intermediate (CD14(high) CD16(high)) and non-classical (CD14(low) CD16(high)) monocytes and surface expression levels of CD14 and CD16 were determined, as well as surface expression of proteinase 3 (PR3) and myeloperoxidase (MPO) on monocyte subsets. There was no change in the proportion of monocytes in each subset in patients with AAV compared with healthy controls. The expression of CD14 on monocytes from patients with active AAV was increased, compared with patients in remission and healthy controls (P < 0.01). Patients with PR3-ANCA disease in remission also had increased monocyte expression of CD14 compared with controls (P < 0.01); however, levels in patients with MPO-ANCA disease in remission were lower than active MPO-ANCA patients, and not significantly different from controls. There was a correlation between CD14 and both PR3 and MPO expression on classical monocytes in AAV patients (r = 0.79, P < 0.0001 and r = 0.42, P < 0.005, respectively). In conclusion, there was an increase in monocyte CD14 expression in active AAV and PR3-ANCA disease in remission. The correlation of CD14 expression with ANCA autoantigen expression in AAV may reflect cell activation, and warrants further investigation into the potential for increased CD14 expression to trigger disease induction or relapse.

Indexed as

AdultAgedAntibodies, Antineutrophil CytoplasmicAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisFemaleFlow CytometryGPI-Linked ProteinsHumansLipopolysaccharide ReceptorsMaleMiddle AgedMonocytesMyeloblastinPeroxidaseReceptors, IgGAntibodies, Antineutrophil CytoplasmicFCGR3B protein, humanGPI-Linked ProteinsLipopolysaccharide ReceptorsMyeloblastinPeroxidaseReceptors, IgGanti-neutrophil cytoplasm antibody (ANCA)monocytemyeloperoxidase (MPO)proteinase 3 (PR3)

Identifiers

PMID25766482
PMCPMC4469156
OpenAlexW1564526535

What OpenQuestion holds

Textmetadata
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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.