Evidence map›Paper›PMID 18384429›Full record

ArticleClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology2008

IL-13 induced increases in nitrite levels are primarily driven by increases in inducible nitric oxide synthase as compared with effects on arginases in human primary bronchial epithelial cells.

K Chibana, J B Trudeau, A T Mustovich, A T Mustovitch, H Hu, J Zhao, S Balzar, H W Chu, S E Wenzel

Erratum issued Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT05870215 (Phenotyping Responses to Systemic Corticosteroids in the Management of Asthma Attacks), which is not on this map. Cited by 93 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed, 2 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.

NCT05870215 completednot on this mapstarted 2022, after this paper: background citation

Phenotyping Responses to Systemic Corticosteroids in the Management of Asthma Attacks (PRISMA): Clinical and Translational Correlation to Point-Of-Care Biomarkers

TypeobservationalSponsorUniversité de SherbrookeRan2022 to 2024Enrolled78ConditionsAsthmaArmsVisit 1: Clinical exam and questionnaires, Visit 1: Respiratory physiology, Visit 1: Inflammometry, Visit 2: Clinical exam and questionnaires, Visit 2: Respiratory physiology
3 · Its place in the literature

Who cites it

93 citing papers in PubMed, 2 syntheses or guidelines pooled it, 205 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
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  6. Trial
  7. Article
  8. Article
  9. Article
  10. HAntioxidants (Basel, Switzerland) · 2026
    Article
  11. Article
  12. Review
  13. Clinical and Biological Features of a Thickened Basement Membrane Zone in Asthma.American journal of respiratory and critical care medicine · 2025
    Article
  14. Article
  15. Review
  16. The epithelial era of asthma research: knowledge gaps and future direction for patient care.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  17. Asthma Pathogenesis: Phenotypes, Therapies, and Gaps: Summary of the Aspen Lung Conference 2023.American journal of respiratory cell and molecular biology · 2024
    Review
  18. Article
  19. SURFACTANT PROTEIN A: AN INNATE IMMUNE MODULATOR AND THERAPEUTIC IN ASTHMA.Transactions of the American Clinical and Climatological Association · 2024
    Review
  20. Review

33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
    Mustovitch, A T [corrected to Mustovich, A T]
5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

K ChibanaDivision of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA. chibanak@upmc.edu
J B Trudeau
A T Mustovich
A T Mustovitch
H Hu
J Zhao
S Balzar
H W Chu
S E Wenzel
University of Pittsburgh Medical Center · USUniversity of Colorado Denver · US

Funding

University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
TGF-BETA AND 15 HETE IN POORLY STEROID RESPONSIVE ASTHMAR01AI040600 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WENZEL, SALLY E · 1997 to 2014
$4.8M
Th2 effects on eicosanoid pathways: implications for altered innate responses inR01AI067780 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WENZEL, SALLY E · 2006 to 2010
$1.8M
NCATS NIH HHS UL1 TR000005NIAID NIH HHS AI-40600NIAID NIH HHS AI-67780NIAID NIH HHS R01 AI040600NIAID NIH HHS R01 AI067780
6 · The paper itself

Abstract

backgroundExhaled nitric oxide is increased in asthma, but the mechanisms controlling its production, including the effects of T-helper type 2 (Th2) cytokines, are poorly understood. In mouse and submerged human epithelial cells, Th2 cytokines inhibit expression of inducible nitric oxide synthase (iNOS). Arginases have been proposed to contribute to asthma pathogenesis by limiting the arginine substrate available to NOS enzymes, but expression of any of these enzymes has not been extensively studied in primary human cells.

objectivesWe hypothesized that primary human airway epithelial cells in air-liquid interface (ALI) culture would increase iNOS expression and activity in response to IL-13, while decreasing arginase expression.

methodsiNOS and arginase mRNA (real-time PCR) and protein expression (Western blot and immunofluorescence) as well as iNOS activity (nitrite levels) were measured in ALI epithelial cells cultured from bronchial brushings of normal and asthmatic subjects following IL-13 stimulation.

resultsIL-13 up-regulated iNOS mRNA primarily at a transcriptional level in epithelial cells. iNOS protein and activity also increased, arginase1 protein expression decreased while arginase 2 expression did not change. The changes in iNOS protein correlated strongly with changes in nitrites, and inclusion of arginase (1 or 2) did not substantially change the relationship. Interestingly, iNOS mRNA and protein were not correlated.

conclusionsThese results contrast with many previous results to confirm that Th2 stimuli enhance iNOS expression and activity. While arginase 1 protein decreases in response to IL-13, neither arginase appears to substantially impact nitrite levels in this system.

Indexed as

AdultArginaseAsthmaBlotting, WesternBronchiBronchoscopyCells, CulturedDose-Response Relationship, DrugEpitheliumFemaleGene Expression RegulationHumansInterferon-gammaInterleukin-13MaleMicroscopy, FluorescenceArginaseInterferon-gammaInterleukin-13Nitric Oxide SynthaseNitric Oxide Synthase Type IINitritesNOS2 protein, humanRNA, Messenger

Identifiers

PMID18384429
PMCPMC11934259
OpenAlexW2043943442

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.