Evidence map›Paper›PMID 24220317›Full record

Trial reportThe Journal of allergy and clinical immunology2014

Increased density of intraepithelial mast cells in patients with exercise-induced bronchoconstriction regulated through epithelially derived thymic stromal lymphopoietin and IL-33.

Ying Lai, William A Altemeier, John Vandree, Adrian M Piliponsky, Brian Johnson, Cara L Appel, Charles W Frevert, Dallas M Hyde, Steven F Ziegler, Dirk E Smith and 3 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

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  16. The Intricate Web of Phospholipase AAmerican journal of respiratory cell and molecular biology · 2020
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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

13 authors at 5 institutions in 2 countries.

Ying LaiDepartment of Medicine, Division of Pulmonary and Critical Care, University of Washington, Seattle, Wash.
William A AltemeierDepartment of Medicine, Division of Pulmonary and Critical Care, University of Washington, Seattle, Wash.
John VandreeDepartment of Medicine, Division of Pulmonary and Critical Care, University of Washington, Seattle, Wash.
Adrian M PiliponskyCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, Wash.
Brian JohnsonDepartment of Comparative Medicine, University of Washington, Seattle, Wash.
Cara L AppelDepartment of Comparative Medicine, University of Washington, Seattle, Wash.
Charles W FrevertDepartment of Comparative Medicine, University of Washington, Seattle, Wash.
Dallas M HydeSchool of Veterinary Medicine, University of California Davis, Davis, Calif.
Steven F ZieglerImmunology Program, Benaroya Research Institute, Seattle, Wash.
Dirk E SmithDepartment of Inflammation Research, Amgen, Seattle, Wash.
William R HendersonDepartment of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Seattle, Wash.
Michael H GelbDepartment of Chemistry, University of Washington, Seattle, Wash; Department of Biochemistry, University of Washington, Seattle, Wash.
Teal S HallstrandDepartment of Medicine, Division of Pulmonary and Critical Care, University of Washington, Seattle, Wash. Electronic address: tealh@u.washington.edu.
University of Washington · USAmgen (Germany) · DEBenaroya Research InstituteSeattle Children's Hospital · USUniversity of California, Davis · US

Funding

Biochemical Studies of 14-kDa Phospholipases A2R37HL036235 · NHLBI · UNIVERSITY OF WASHINGTON · PI GELB, MICHAEL H · 2007 to 2016
$4.1M
Secretory Phospholipase A2s in Airway PathophysiologyR01HL089215 · NHLBI · UNIVERSITY OF WASHINGTON · PI HALLSTRAND, TEAL S · 2008 to 2017
$4.0M
Critical role of chymase in the regulation of inflammation and survival in sepsisR01HL113351 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI PILIPONSKY, ADRIAN M · 2012 to 2016
$2.4M
NHLBI NIH HHS R01 HL089215NHLBI NIH HHS R01HL089215NHLBI NIH HHS R01 HL113351NHLBI NIH HHS R37 HL036235NHLBI NIH HHS R37HL036235
6 · The paper itself

Abstract

backgroundExercise-induced bronchoconstriction (EIB) is a prototypical feature of indirect airway hyperresponsiveness. Mast cells are implicated in EIB, but the characteristics, regulation, and function of mast cells in patients with EIB are poorly understood.

objectivesWe sought to examine mast cell infiltration of the airway epithelium in patients with EIB and the regulation of mast cell phenotype and function by epithelially derived cytokines.

methodsEndobronchial biopsy specimens, epithelial brushings, and induced sputum were obtained from asthmatic patients with and without EIB and healthy control subjects. Mast cell proteases were quantified by using quantitative PCR, and mast cell density was quantified by using design-based stereology. Airway epithelial responses to wounding and osmotic stress were assessed in primary airway epithelial cells and ex vivo murine lung tissue. Mast cell granule development and function were examined in cord blood-derived mast cells.

resultsTryptase and carboxypeptidase A3 expression in epithelial brushings and epithelial mast cell density were selectively increased in the asthma group with EIB. An in vitro scratch wound initiated the release of thymic stromal lymphopoietin, which was greater in epithelial cells derived from asthmatic patients. Osmotic stress induced the release of IL-33 from explanted murine lungs, which was increased in allergen-treated mice. Thymic stromal lymphopoietin combined with IL-33 increased tryptase and carboxypeptidase A3 immunostaining in mast cell precursors and selectively increased cysteinyl leukotriene formation by mast cells in a manner that was independent of in vitro sensitization.

conclusionsMast cell infiltration of the epithelium is a critical determinant of indirect airway hyperresponsiveness, and the airway epithelium might serve as an important regulator of the development and function of this mast cell population.

Indexed as

AnimalsAsthma, Exercise-InducedCell LineCytokinesFemaleGene Expression RegulationHumansInterleukin-33InterleukinsLungMaleMast CellsMiceRespiratory MucosaSputumThymic Stromal LymphopoietinCytokinesIL33 protein, humanInterleukin-33InterleukinsThymic Stromal Lymphopoietinairway hyperresponsivenessAsthmaeicosanoidepithelial cellleukotriene

Identifiers

PMID24220317
PMCPMC4004718
OpenAlexW2027278345

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.