Evidence map›Paper›PMID 42150103›Full record

ArticleAmerican journal of respiratory and critical care medicine2026

Airway microbiome diversity, intramucosal bacteria, and spatial immunity in asthmatic adults and controls.

Miriam F Moffatt, Tamiko Nishimura, Michael J Cox, Claire McBrien, Conor Burke, Leah Cuthbertson, Keir Lewis, Richard Attanoos, Gwyneth A Davies, Kian Fan Chung and 9 more

Abstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Miriam F MoffattNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Tamiko NishimuraVictor Phillip Dahdaleh Institute of Genomic Medicine, McGill University, Montréal, Canada.
Michael J CoxDepartment of Microbes, Infection and Microbiomes, School of Infection, Inflammation and Immunology, College of Medicine and Health, University of Birmingham, Birmingham, United Kingdom.
Claire McBrienNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Conor BurkeDepartment of Respiratory Medicine, Connolly Hospital, Dublin, Ireland.
Leah CuthbertsonNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Keir LewisRespiratory Medicine, Hywel Dda University Health Board, Llanelli, United Kingdom.
Richard AttanoosUniversity Hospital of Wales and School of Biosciences, Cardiff University, Cardiff, United Kingdom.
Gwyneth A DaviesFaculty of Medicine, Health and Life Science, Swansea University, Swansea, United Kingdom.
Kian Fan ChungNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Jan Lukas RobertusNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Jonathan Ish-HorowiczNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Orla O'CarrollDepartment of Respiratory Medicine, Connolly Hospital, Dublin, Ireland.
John M BozemanNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Aisling McGowanDepartment of Respiratory Medicine, Connolly Hospital, Dublin, Ireland.
Julian M HopkinUniversity Hospital of Wales and School of Biosciences, Cardiff University, Cardiff, United Kingdom.
G Mark LathropVictor Phillip Dahdaleh Institute of Genomic Medicine, McGill University, Montréal, Canada.
Yasser RiazalhosseiniVictor Phillip Dahdaleh Institute of Genomic Medicine, McGill University, Montréal, Canada.
William O C CooksonNational Heart and Lung Institute, Imperial College London, London, United Kingdom.

Funding

Asmarley TrustWellcome WT096964MAWellcome WT097117MAWellcome Trust 215359/Z/19/Z
6 · The paper itself

Abstract

rationaleAsthma is characterized by disruption of the thoracic airway mucosae and loss of microbial diversity. Spatial profiling of the mucosal transcriptome may systematically discover mechanisms for microbial influences on immunity.

objectivesWe investigated relationships between clinical measures, microbial communities, and the host mucosal transcriptome within different strata of bronchial biopsies in subjects with and without asthma.

methodsWe performed bronchoscopy in 65 asthmatic adults and 44 healthy controls, quantifying bacterial operational taxonomic units (OTUs) in bronchial brushings by 16S ribosomal RNA (rRNA) gene amplicon sequences. Biopsy histologic features were scored blind to diagnosis. Following 16S rRNA in situ hybridization of 44 biopsies, bacterial foci were scored in epithelium, basement membrane, and stroma. Global human gene expression was quantified in epithelial and stromal compartments using digital spatial profiling. MEASUREMENTS AND MAIN

resultsClinical asthma was independently predicted by basement membrane abnormalities (BaseMA), endobronchial bacterial diversity, and circulating eosinophil counts, but not by specific OTU abundances. 16S rRNA staining revealed bacteria within epithelium and mucosa of all biopsies. Intramucosal bacteria counts correlated negatively with spatially organized coexpression networks encoding antigen-specific immunity, neutrophil functions, and matrix activation, whereas BaseMA correlated positively with the adaptive immunity module. Eosinophil counts correlated with epithelial bacterial counts and senescence pathways. Clinical asthma was accompanied by upregulation of a regulatory T-cell network.

conclusionsAsthma and its related phenotypes are accompanied by complex mucosal events that extend beyond eosinophilic pathways. Components of diverse airway microbiota may modify immunity by beneficial interactions within the mucosa.

Indexed as

AsthmaBronchiMicrobiotaRespiratory MucosaAdultBiopsyBronchoscopyCase-Control StudiesFemaleHumansMaleMiddle AgedRNA, Ribosomal, 16SRNA, Ribosomal, 16Sairway microbiomeasthmadiversityendosymbiosisstroma

Identifiers

PMID42150103
PMCPMC13519334

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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.