Evidence map›Paper›PMID 24890720›Full record

Trial reportJournal of immunology (Baltimore, Md. : 1950)2014

Aspirin activation of eosinophils and mast cells: implications in the pathogenesis of aspirin-exacerbated respiratory disease.

John W Steinke, Julie Negri, Lixia Liu, Spencer C Payne, Larry Borish

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Utility of low-dose oral aspirin challenges for diagnosis of aspirin-exacerbated respiratory disease.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2016
    Trial
  3. Article
  4. Mast Cells in Aspirin-Exacerbated Respiratory Disease.Current allergy and asthma reports · 2024
    Review
  5. An Update on Nonsteroidal Anti-Inflammatory Drug-Induced Urticaria.Endocrine, metabolic & immune disorders drug targets · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Suppression of aspirin-mediated eosinophil activation by prostaglandin EAnnals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2019
    Article
  15. Leukotriene A4 Hydrolase Activation and Leukotriene B4 Production by Eosinophils in Severe Asthma.American journal of respiratory cell and molecular biology · 2019
    Article
  16. Review
  17. Review
  18. Eosinophils and Mast Cells in Aspirin-Exacerbated Respiratory Disease.Immunology and allergy clinics of North America · 2016
    Review
  19. Review
  20. Eosinophil production of prostaglandin DThe Journal of allergy and clinical immunology · 2016
    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

5 authors at 1 institution in 1 country.

John W SteinkeAsthma and Allergic Disease Center, Department of Medicine, University of Virginia Health System, Charlottesville, VA 22908; Carter Immunology Center, University of Virginia Health System, Charlottesville, VA 22908; and.
Julie NegriAsthma and Allergic Disease Center, Department of Medicine, University of Virginia Health System, Charlottesville, VA 22908; Carter Immunology Center, University of Virginia Health System, Charlottesville, VA 22908; and.
Lixia LiuAsthma and Allergic Disease Center, Department of Medicine, University of Virginia Health System, Charlottesville, VA 22908; Carter Immunology Center, University of Virginia Health System, Charlottesville, VA 22908; and.
Spencer C PayneAsthma and Allergic Disease Center, Department of Medicine, University of Virginia Health System, Charlottesville, VA 22908; Carter Immunology Center, University of Virginia Health System, Charlottesville, VA 22908; and Department of Otolaryngology-Head and Neck Surgery, University of Virginia Health System, Charlottesville, VA 22908.
Larry BorishAsthma and Allergic Disease Center, Department of Medicine, University of Virginia Health System, Charlottesville, VA 22908; Carter Immunology Center, University of Virginia Health System, Charlottesville, VA 22908; and lb4m@virginia.edu.
University of Virginia Health System · US

Funding

An Evaluation of Treatment with Omalizumab to Improve the Asthmatic Response to aU01AI100799 · NIAID · UNIVERSITY OF VIRGINIA · PI HEYMANN, PETER W, PLATTS-MILLS, THOMAS A. · 2012 to 2015
$5.3M
Viruses and IgE in relation to mechanisms of asthmaP01AI050989 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI PLATTS-MILLS, THOMAS A. · 2001 to 2005
$4.9M
Interplay between LTE4/LTE4 receptors and IFN-y with mast cells and eosinophils iR01AI057438 · NIAID · UNIVERSITY OF VIRGINIA · PI BORISH, LARRY C · 2006 to 2015
$3.7M
RECOMBINANT HUMAN INTERLEUKIN-4 RECEPTOR IN ASTHMAR01AI047737 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BORISH, LARRY C · 2000 to 2004
$1.3M
CD4+ and CD8+ T cell dependent immune mechanisms of rhinovirus-mediated asthma exR21AI090413 · NIAID · UNIVERSITY OF VIRGINIA · PI BORISH, LARRY C · 2010 to 2011
$422k
NIAID NIH HHS P01 AI050989NIAID NIH HHS P01-AI50989NIAID NIH HHS R01 AI047737NIAID NIH HHS R01 AI057438NIAID NIH HHS R01-AI47737NIAID NIH HHS R21 AI090413NIAID NIH HHS U01 AI100799
6 · The paper itself

Abstract

Reactions to aspirin and nonsteroidal anti-inflammatory drugs in patients with aspirin-exacerbated respiratory disease (AERD) are triggered when constraints upon activated eosinophils, normally supplied by PGE2, are removed secondary to cyclooxygenase-1 inhibition. However, the mechanism driving the concomitant cellular activation is unknown. We investigated the capacity of aspirin itself to provide this activation signal. Eosinophils were enriched from peripheral blood samples and activated with lysine ASA (LysASA). Parallel samples were stimulated with related nonsteroidal anti-inflammatory drugs. Activation was evaluated as Ca2+ flux, secretion of cysteinyl leukotrienes (CysLT), and eosinophil-derived neurotoxin (EDN) release. CD34+ progenitor-derived mast cells were also used to test the influence of aspirin on human mast cells with measurements of Ca2+ flux and PGD2 release. LysASA induced Ca2+ fluxes and EDN release, but not CysLT secretion from circulating eosinophils. There was no difference in the sensitivity or extent of activation between AERD and control subjects, and sodium salicylate was without effect. Like eosinophils, aspirin was able to activate human mast cells directly through Ca2+ flux and PGD2 release. AERD is associated with eosinophils maturing locally in a high IFN-γ milieu. As such, in additional studies, eosinophil progenitors were differentiated in the presence of IFN-γ prior to activation with aspirin. Eosinophils matured in the presence of IFN-γ displayed robust secretion of both EDN and CysLTs. These studies identify aspirin as the trigger of eosinophil and mast cell activation in AERD, acting in synergy with its ability to release cells from the anti-inflammatory constraints of PGE2.

Indexed as

AspirinAsthma, Aspirin-InducedCalcium SignalingCyclooxygenase InhibitorsCysteineEosinophil-Derived NeurotoxinEosinophilsFemaleHumansInterferon-gammaLeukotrienesMaleMast CellsProstaglandin D2AspirinCyclooxygenase InhibitorsCysteinecysteinyl-leukotrieneEosinophil-Derived NeurotoxinIFNG protein, humanInterferon-gammaLeukotrienesProstaglandin D2

Identifiers

PMID24890720
PMCPMC4065844
OpenAlexW1944449548

What OpenQuestion holds

Textmetadata
LicenceTDM
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.