Evidence map›Paper›PMID 30682383›Full record

ArticleToxicology and applied pharmacology2019

Quantum dots and mouse strain influence house dust mite-induced allergic airway disease.

David K Scoville, James D Nolin, H Luke Ogden, Dowon An, Zahra Afsharinejad, Brian W Johnson, Theo K Bammler, Xiaohu Gao, Charles W Frevert, William A Altemeier and 2 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Toxicology and applied pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  5. Secreted Phospholipase AJournal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  6. Review
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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

12 authors at 1 institution in 1 country.

David K ScovilleDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195, USA.
James D NolinDepartment of Medicine, University of Washington, Seattle, WA 98195, USA.
H Luke OgdenDepartment of Medicine, University of Washington, Seattle, WA 98195, USA.
Dowon AnDepartment of Medicine, University of Washington, Seattle, WA 98195, USA.
Zahra AfsharinejadDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195, USA.
Brian W JohnsonDepartment of Comparative Medicine, University of Washington, Seattle, WA 98195, USA.
Theo K BammlerDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195, USA.
Xiaohu GaoDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Charles W FrevertDepartment of Comparative Medicine, University of Washington, Seattle, WA 98195, USA.
William A AltemeierDepartment of Medicine, University of Washington, Seattle, WA 98195, USA.
Teal S HallstrandDepartment of Medicine, University of Washington, Seattle, WA 98195, USA.
Terrance J KavanaghDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195, USA. Electronic address: tjkav@uw.edu.
University of Washington · US

Funding

XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI Sheela Sathyanarayana · 1995 to 2026
$42.5M
Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Christopher Hooper Goss, Lucas R Hoffman · 2010 to 2026
$21.4M
Biostatistics, Epidemiologic & Bioinformatic Training in Environmental HealthT32ES015459 · NIEHS · UNIVERSITY OF WASHINGTON · PI June T. Spector · 2009 to 2026
$10.6M
Regulation of the Innate Immune Response by the Epithelium in AsthmaU19AI125378 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J · 2016 to 2020
$9.2M
Project 3: Integrative Risk Assessment Methods for Engineered NanomaterialsU19ES019545 · NIEHS · UNIVERSITY OF WASHINGTON · PI KAVANAGH, TERRANCE J · 2010 to 2014
$5.6M
Secretory Phospholipase A2s in Airway PathophysiologyR01HL089215 · NHLBI · UNIVERSITY OF WASHINGTON · PI HALLSTRAND, TEAL S · 2008 to 2017
$4.0M
PDGFR-beta+ stromal cells as critical regulators of immune response to tissue injuryR01HL122895 · NHLBI · UNIVERSITY OF WASHINGTON · PI ALTEMEIER, WILLIAM A · 2015 to 2018
$1.7M
Immunopathology of Indirect Airway Hyperresponsiveness in AsthmaK24AI130263 · NIAID · UNIVERSITY OF WASHINGTON · PI Teal S Hallstrand · 2017 to 2026
$1.3M
Secreted Phospholipase A2 Group X Regulation of Type-2 InflammationF32HL134217 · NHLBI · UNIVERSITY OF WASHINGTON · PI NOLIN, JAMES D · 2017 to 2018
$90k
NHLBI NIH HHS F32 HL134217NHLBI NIH HHS R01 HL089215NHLBI NIH HHS R01 HL122895NIAID NIH HHS K24 AI130263NIAID NIH HHS U19 AI125378NIDDK NIH HHS P30 DK089507NIEHS NIH HHS P30 ES007033NIEHS NIH HHS T32 ES015459NIEHS NIH HHS U19 ES019545
6 · The paper itself

Abstract

Quantum dot nanoparticles (QDs) are engineered nanomaterials (ENMs) that have utility in many industries due to unique optical properties not available in small molecules or bulk materials. QD-induced acute lung inflammation and toxicity in rodent models raise concerns about potential human health risks. Recent studies have also shown that some ENMs can exacerbate allergic airway disease (AAD). In this study, C57BL/6J and A/J mice were exposed to saline, house dust mite (HDM), or a combination of HDM and QDs on day 1 of the sensitization protocol. Mice were then challenged on days 8, 9 and 10 with HDM or saline only. Significant differences in cellular and molecular markers of AAD induced by both HDM and HDM + QD were observed between C57BL/6J and A/J mice. Among A/J mice, HDM + QD co-exposure, but not HDM exposure alone, significantly increased levels of bronchoalveolar lavage fluid (BALF). IL-33 compared to saline controls. BALF total protein levels in both mouse strains were also only significantly increased by HDM + QD co-exposure. In addition, A/J mice had significantly more lung type 2 innate lymphoid cells (ILC2s) cells than C57BL/6J mice. A/J lung ILC2s were inversely correlated with lung glutathione and MHC-II

Indexed as

AnimalsAntigens, DermatophagoidesCytokinesDisease Models, AnimalGenotypeInflammation MediatorsInsect ProteinsLungMaleMice, Inbred C57BLPhenotypePyroglyphidaeQuantum DotsRespiratory HypersensitivityRisk FactorsSpecies SpecificityAntigens, DermatophagoidesCytokinesInflammation MediatorsInsect Proteins

Identifiers

PMID30682383
PMCPMC7737882
OpenAlexW2912557632

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.