Evidence map›Paper›PMID 42807828›Full record

ArticleERJ open research2026

Relationships between basement membrane zone thickness and airway physiology, epithelial gene expression and innate immune cell infiltration in asthma.

Matthew Liu, Ryan C Murphy, Ashley Mazzotta, Ying Lai, Jonathan Lee, Stephen R Reeves, Teal S Hallstrand

Abstract read
In one paragraph

Article in ERJ open research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Matthew LiuDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep, University of Washington, Seattle, WA, USA.
Ryan C MurphyDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep, University of Washington, Seattle, WA, USA.ORCID https://orcid.org/0000-0003-0094-0003
Ashley MazzottaDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep, University of Washington, Seattle, WA, USA.
Ying LaiDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep, University of Washington, Seattle, WA, USA.
Jonathan LeeDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep, University of Washington, Seattle, WA, USA.
Stephen R ReevesDepartment of Pediatrics, Division of Pulmonary and Sleep Medicine, Seattle Children's Hospital, University of Washington, Seattle, WA, USA.ORCID https://orcid.org/0000-0002-8552-6022
Teal S HallstrandDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep, University of Washington, Seattle, WA, USA.

Funding

The Bioinformatics and Data Management Core (BDMC)U19AI175089 · NIAID · UNIVERSITY OF WASHINGTON · PI JASON S DEBLEY, Teal S Hallstrand · 2023 to 2026
$7.8M
Origin and Function of Intra-epithelial Mast Cells in AsthmaR01HL153979 · NHLBI · UNIVERSITY OF WASHINGTON · PI HALLSTRAND, TEAL S · 2021 to 2024
$2.9M
Immunopathology of Indirect Airway Hyperresponsiveness in AsthmaK24AI130263 · NIAID · UNIVERSITY OF WASHINGTON · PI Teal S Hallstrand · 2017 to 2026
$1.3M
NHLBI NIH HHS R01 HL153979NIAID NIH HHS K24 AI130263NIAID NIH HHS U19 AI175089
6 · The paper itself

Abstract

Rationale: Thickening of the basement membrane zone (BMZ) has often been identified in airway biopsies of individuals with asthma, but the relationship of BMZ thickness to airway dysfunction and inflammation is incompletely understood. The objectives of the present study were to characterise the relationship between BMZ thickness and airway physiology, immune cell infiltration and airway gene expression. Methods: We used design-based stereology to measure BMZ thickness in endobronchial biopsy samples obtained from 10 healthy control subjects and 31 individuals with asthma not receiving asthma-directed anti-inflammatory therapies (only using as-needed albuterol for the study period). BMZ thickness was correlated with measures of airway physiology, sputum inflammatory markers, airway wall immunopathology and gene expression from airway epithelial brushings. Results: Individuals with asthma had a significantly thicker BMZ relative to healthy controls. BMZ thickness was negatively correlated with age and positively correlated with higher baseline lung function (forced vital capacity), mast cell (MC) infiltration of the airway epithelial compartment and expression of type 2 (T2) inflammatory genes in the airway. Thickening of the BMZ was not significantly associated with the bronchodilator response, direct airway hyperresponsiveness (AHR) to methacholine, indirect AHR in the form of exercise-induced bronchoconstriction, T1 or T3 inflammation, or airway eosinophilia. Conclusions: MC infiltration of the airway epithelial compartment and T2 inflammation are significantly associated with a thickened BMZ in asthma.

Identifiers

PMID42807828
PMCPMC13617596

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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.