Evidence map›Paper›PMID 17293377›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2007

Nonhematopoietic NADPH oxidase regulation of lung eosinophilia and airway hyperresponsiveness in experimentally induced asthma.

Hiam Abdala-Valencia, Julie Earwood, Shelly Bansal, Michael Jansen, George Babcock, Beth Garvy, Marsha Wills-Karp, Joan M Cook-Mills

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

41 citing papers in PubMed, 56 citations in OpenAlex.

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  15. Interaction between allergic asthma and atherosclerosis.Translational research : the journal of laboratory and clinical medicine · 2016
    Review
  16. Article
  17. Regulation of allergic lung inflammation by endothelial cell transglutaminase 2.American journal of physiology. Lung cellular and molecular physiology · 2015
    Article
  18. Review
  19. Article
  20. 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 3 institutions in 1 country.

Hiam Abdala-ValenciaAllergy-Immunology Division, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA.
Julie Earwood
Shelly Bansal
Michael Jansen
George Babcock
Beth Garvy
Marsha Wills-Karp
Joan M Cook-Mills
University of Cincinnati · USCincinnati Children's Hospital Medical Center · USUniversity of Kentucky · US

Funding

gp91 phox Function in VCAM-1-dependent Lung EosinophiliaR01HL069428 · NHLBI · UNIVERSITY OF CINCINNATI · PI COOK-MILLS, JOAN M · 2005 to 2008
$1.3M
NHLBI NIH HHS R01 HL069428NHLBI NIH HHS R01-HL-069428
6 · The paper itself

Abstract

Pulmonary eosinophilia is one of the most consistent hallmarks of asthma. Infiltration of eosinophils into the lung in experimental asthma is dependent on the adhesion molecule vascular cell adhesion molecule-1 (VCAM-1) on endothelial cells. Ligation of VCAM-1 activates endothelial cell NADPH oxidase, which is required for VCAM-1-dependent leukocyte migration in vitro. To examine whether endothelial-derived NADPH oxidase modulates eosinophil recruitment in vivo, mice deficient in NADPH oxidase (CYBB mice) were irradiated and received wild-type hematopoietic cells to generate chimeric CYBB mice. In response to ovalbumin (OVA) challenge, the chimeric CYBB mice had increased numbers of eosinophils bound to the endothelium as well as reduced eosinophilia in the lung tissue and bronchoalveolar lavage. This occurred independent of changes in VCAM-1 expression, cytokine/chemokine levels (IL-5, IL-10, IL-13, IFNgamma, or eotaxin), or numbers of T cells, neutrophils, or mononuclear cells in the lavage fluids or lung tissue of OVA-challenged mice. Importantly, the OVA-challenged chimeric CYBB mice had reduced airway hyperresponsiveness (AHR). The AHR in OVA-challenged chimeric CYBB mice was restored by bypassing the endothelium with intratracheal administration of eosinophils. These data suggest that VCAM-1 induction of NADPH oxidase in the endothelium is necessary for the eosinophil recruitment during allergic inflammation. Moreover, these studies provide a basis for targeting VCAM-1-dependent signaling pathways in asthma therapies.

Indexed as

AnimalsAsthmaBronchial HyperreactivityChemokine CCL11Chemokines, CCCytokinesDisease Models, AnimalEndothelium, VascularMiceMice, Inbred C57BLMice, Inbred StrainsNADPH OxidasesOvalbuminPulmonary EosinophiliaVascular Cell Adhesion Molecule-1Ccl11 protein, mouseChemokine CCL11Chemokines, CCCytokinesNADPH OxidasesOvalbuminVascular Cell Adhesion Molecule-1

Identifiers

PMID17293377
PMCPMC2710034
OpenAlexW2104152732

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.