Evidence map›Paper›PMID 26374606›Full record

ArticleJournal of the American Society of Nephrology : JASN2016

Mast Cell Stabilization Ameliorates Autoimmune Anti-Myeloperoxidase Glomerulonephritis.

Poh-Yi Gan, Kim M O'Sullivan, Joshua D Ooi, Maliha A Alikhan, Dragana Odobasic, Shaun A Summers, A Richard Kitching, Stephen R Holdsworth

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Mast cells: a double-edged sword in inflammation and fibrosis.Frontiers in cell and developmental biology · 2024
    Review
  7. Review
  8. Mast cell activation and degranulation in acute artery injury: A target for post-operative therapy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Animal Models of ANCA Associated Vasculitis.Frontiers in immunology · 2020
    Review
  15. Review
  16. Article
  17. Review
  18. 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

8 authors at 2 institutions in 1 country.

Poh-Yi GanCentre for Inflammatory Diseases, Monash University Department of Medicine, Clayton, VIC, Australia; and.
Kim M O'SullivanCentre for Inflammatory Diseases, Monash University Department of Medicine, Clayton, VIC, Australia; and.
Joshua D OoiCentre for Inflammatory Diseases, Monash University Department of Medicine, Clayton, VIC, Australia; and.
Maliha A AlikhanCentre for Inflammatory Diseases, Monash University Department of Medicine, Clayton, VIC, Australia; and.
Dragana OdobasicCentre for Inflammatory Diseases, Monash University Department of Medicine, Clayton, VIC, Australia; and.
Shaun A SummersCentre for Inflammatory Diseases, Monash University Department of Medicine, Clayton, VIC, Australia; and.
A Richard KitchingCentre for Inflammatory Diseases, Monash University Department of Medicine, Clayton, VIC, Australia; and Department of Nephrology, Monash Health, 246 Clayton Road, Clayton, VIC 3168, Australia.
Stephen R HoldsworthCentre for Inflammatory Diseases, Monash University Department of Medicine, Clayton, VIC, Australia; and Department of Nephrology, Monash Health, 246 Clayton Road, Clayton, VIC 3168, Australia Stephen.holdsworth@monash.edu.
Monash University · AUMonash Health · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Observations in experimental murine myeloperoxidase (MPO)-ANCA-associated vasculitis (AAV) show mast cells degranulate, thus enhancing injury as well as producing immunomodulatory IL-10. Here we report that, compared with biopsy specimens from control patients, renal biopsy specimens from 44 patients with acute AAV had more mast cells in the interstitium, which correlated with the severity of tubulointerstitial injury. Furthermore, most of the mast cells were degranulated and spindle-shaped in patients with acute AAV, indicating an activated phenotype. We hypothesized that the mast cell stabilizer disodium cromoglycate would attenuate mast cell degranulation without affecting IL-10 production. We induced anti-MPO GN by immunizing mice with MPO and a low dose of anti-glomerular basement membrane antibody. When administered before or after induction of MPO autoimmunity in these mice, disodium cromoglycate attenuated mast cell degranulation, development of autoimmunity, and development of GN, without diminishing IL-10 production. In contrast, administration of disodium cromoglycate to mast cell-deficient mice had no effect on the development of MPO autoimmunity or GN. MPO-specific CD4(+) effector T cell proliferation was enhanced by co-culture with mast cells, but in the presence of disodium cromoglycate, proliferation was inhibited and IL-10 production was enhanced. These results indicate that disodium cromoglycate blocks injurious mast cell degranulation specifically without affecting the immunomodulatory role of these cells. Thus as a therapeutic, disodium cromoglycate may substantially enhance the regulatory role of mast cells in MPO-AAV.

Indexed as

AgedAnimalsAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisAutoimmune DiseasesCromolyn SodiumFemaleGlomerulonephritisHumansMaleMast CellsMicePeroxidaseCromolyn SodiumPeroxidase

Identifiers

PMID26374606
PMCPMC4849811
OpenAlexW2175530565

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.