Evidence map›Paper›PMID 39326914›Full record

ArticleThe European respiratory journal2024

Single-cell sequencing reveals cellular landscape alterations in the airway mucosa of patients with pulmonary long COVID.

Firoozeh V Gerayeli, Hye Yun Park, Stephen Milne, Xuan Li, Chen Xi Yang, Josie Tuong, Rachel L Eddy, Seyed Milad Vahedi, Elizabeth Guinto, Chung Y Cheung and 11 more

Abstract read
In one paragraph

Article in The European respiratory journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  11. A proposed approach to pulmonary long COVID: a viewpoint.The European respiratory journal · 2024
    Article
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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

21 authors.

Firoozeh V GerayeliCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Hye Yun ParkCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Stephen MilneCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.ORCID https://orcid.org/0000-0001-5274-1298
Xuan LiCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Chen Xi YangCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.ORCID https://orcid.org/0000-0002-8033-4769
Josie TuongCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Rachel L EddyCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Seyed Milad VahediCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Elizabeth GuintoCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.ORCID https://orcid.org/0000-0002-4239-0006
Chung Y CheungCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Julia S W YangCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Cassie GilchristCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Dina Yehia
Tara StachBiomedical Research Centre, School of Biomedical Engineering, UBC, Vancouver, BC, Canada.
Hong DangUniversity of North Carolina Chapel Hill, Cystic Fibrosis and Pulmonary Disease Research and Treatment Center, Chapel Hill, NC, USA.
Clarus LeungCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.ORCID https://orcid.org/0000-0003-3515-7537
Tawimas ShaipanichDivision of Respiratory Medicine, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Jonathon LeipsicDepartment of Radiology, University of British Columbia, Vancouver, BC, Canada.
Graeme J KoelwynCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Janice M LeungCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Don D SinCentre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada Don.Sin@hli.ubc.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo elucidate the important cellular and molecular drivers of pulmonary long COVID, we generated a single-cell transcriptomic map of the airway mucosa using bronchial brushings from patients with long COVID who reported persistent pulmonary symptoms.

methodAdults with and without long COVID were recruited from the general community in Greater Vancouver, Canada. The cohort was divided into those with pulmonary long COVID, which was defined as persons with new or worsening respiratory symptoms following ≥12 weeks from their initial acute severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection (n=9); and control subjects defined as SARS-CoV-2 infected persons whose acute respiratory symptoms had fully resolved or individuals who had no history of acute coronavirus disease 2019 (COVID-19) (n=9). These participants underwent bronchoscopy from which a single cell suspension was created from bronchial brush samples and then sequenced.

resultsA total of 56 906 cells were recovered for the downstream analysis, with 34 840 cells belonging to the pulmonary long COVID group, which strikingly showed a unique cluster of neutrophils in the pulmonary long COVID group (p<0.05). Ingenuity Pathway Analysis revealed that the neutrophil degranulation pathway was enriched across epithelial cell clusters. Differential gene expression analysis between the pulmonary long COVID and control groups demonstrated upregulation of inflammatory chemokines and epithelial barrier dysfunction across epithelial cell clusters, as well as over-expression of mucin genes across secretory cell clusters.

conclusionA single-cell transcriptomic landscape of the small airways suggest that neutrophils may play a significant role in mediating the chronic small airway inflammation driving pulmonary symptoms of long COVID.

Indexed as

COVID-19Respiratory MucosaSARS-CoV-2Single-Cell AnalysisAdultAgedBronchoscopyCase-Control StudiesFemaleHumansMaleMiddle AgedNeutrophilsPost-Acute COVID-19 SyndromeTranscriptome

Identifiers

PMID39326914
PMCPMC11602667

What OpenQuestion holds

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LicenceCC BY-NC
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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.