Evidence map›Paper›PMID 33478982›Full record

ArticleImmunoHorizons2021

Barrier Housing and Gender Effects on Allergic Airway Disease in a Murine House Dust Mite Model.

Kelly Weiss, Nicholas Wanner, Kimberly Queisser, Matthew Frimel, Tina Nunn, Timothy Myshrall, Naseer Sangwan, Serpil Erzurum, Kewal Asosingh

Open access · goldAbstract read
In one paragraph

Article in ImmunoHorizons, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-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

21 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. The testosterone paradox in asthma.Frontiers in allergy · 2026
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  5. TLR4Nature communications · 2025
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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

9 authors at 2 institutions in 1 country.

Kelly WeissDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland, OH 44195.
Nicholas WannerDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland, OH 44195.ORCID 0000-0003-1156-1527
Kimberly QueisserDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland, OH 44195.ORCID 0000-0003-1561-8623
Matthew FrimelDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland, OH 44195.
Tina NunnCenter for Microbiome and Human Health, Lerner Research Institute, Cleveland, OH 44195.
Timothy MyshrallBiological Resource Unit, Lerner Research Institute, Cleveland, OH 44195; and.
Naseer SangwanCenter for Microbiome and Human Health, Lerner Research Institute, Cleveland, OH 44195.
Serpil ErzurumDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland, OH 44195.
Kewal AsosinghDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland, OH 44195; asosink@ccf.org.
Cleveland Clinic Lerner College of Medicine · USCleveland Clinic · US

Funding

Targeting pathological hyaluronan matricesP01HL103453 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI ERZURUM, SERPIL C. · 2011 to 2020
$26.8M
Tissue Processing and Cell Culture COreP01HL081064 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI ERZURUM, SERPIL C. · 2006 to 2019
$17.8M
NITRIC OXIDE PRODUCTION AND REACTIONS IN THE LUNGR01HL060917 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI Serpil C. Erzurum · 1999 to 2026
$6.3M
Airway redox biochemistry as a deteriminant of asthma phenotype during adolescen*U10HL109250 · NHLBI · UNIVERSITY OF VIRGINIA · PI ERZURUM, SERPIL C., GASTON, BENJAMIN · 2011 to 2016
$4.2M
Nitric Oxide in Pulmonary HypertensionR37HL060917 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI ERZURUM, SERPIL C. · 2009 to 2018
$3.9M
NHLBI NIH HHS P01 HL081064NHLBI NIH HHS P01 HL103453NHLBI NIH HHS R01 HL060917NHLBI NIH HHS R37 HL060917NHLBI NIH HHS U10 HL109250
6 · The paper itself

Abstract

Allergic airway disease models use laboratory mice housed in highly controlled and hygienic environments, which provide a barrier between the mice and a predetermined list of specific pathogens excluded from the facility. In this study, we hypothesized that differences in facility barrier level and, consequently, the hygienic quality of the environment that mice inhabit impact the severity of pulmonary inflammation and lung function. Allergen-naive animals housed in the cleaner, high barrier (HB) specific pathogen-free facility had increased levels of inflammatory cytokines and higher infiltration of immune cells in the lung tissue but not in the bronchoalveolar lavage compared with mice housed in the less hygienic, low barrier specific pathogen-free facility. In both genders, house dust mite-induced airway disease was more severe in the HB than the low barrier facility. Within each barrier facility, female mice developed the most severe inflammation. However, allergen-naive male mice had worse lung function, regardless of the housing environment, and in the HB, the lung function in female mice was higher in the house dust mite model. Severe disease in the HB was associated with reduced lung microbiome diversity. The lung microbiome was altered across housing barriers, gender, and allergen-exposed groups. Thus, the housing barrier level impacts microbial-driven disease and gender phenotypes in allergic asthma. The housing of laboratory mice in more clean HB facilities aggravates lung immunity and causes a more severe allergic lung disease.

Indexed as

HousingAnimalsAsthmaCytokinesDustFemaleImmunoglobulin ELungMaleMiceMice, Inbred C57BLPyroglyphidaeRespiratory HypersensitivitySex FactorsCytokinesDustImmunoglobulin E

Identifiers

PMID33478982
PMCPMC9404370
OpenAlexW3125706985

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.