Evidence map›Paper›PMID 34232770›Full record

ArticleAmerican journal of rhinology & allergy2022

Regulation of the Expression of SARS-CoV-2 Receptor Angiotensin-Converting Enzyme 2 in Nasal Mucosa.

Tetsuji Takabayashi, Kanako Yoshida, Yoshimasa Imoto, Robert P Schleimer, Shigeharu Fujieda

Open access · bronzeAbstract read
In one paragraph

Article in American journal of rhinology & allergy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

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  6. Fullerenol CInternational journal of nanomedicine · 2024
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  12. A Review of the Role of Pollen in COVID-19 Infection.International journal of environmental research and public health · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Chronic Rhinosinusitis and COVID-19.The journal of allergy and clinical immunology. In practice · 2022
    Review
  18. Article
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

5 authors at 2 institutions in 2 countries.

Tetsuji Takabayashi26423University of Fukui, Yoshida-gun, Fukui, Japan.
Kanako Yoshida26423University of Fukui, Yoshida-gun, Fukui, Japan.
Yoshimasa Imoto26423University of Fukui, Yoshida-gun, Fukui, Japan.
Robert P Schleimer12244Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Shigeharu Fujieda26423University of Fukui, Yoshida-gun, Fukui, Japan.
University of Fukui · JPNorthwestern University · US

Funding

Initiators, biomarkers and mechanisms of epithelial dysfunction and immune pathogenesis in chronic rhinosinusitis and aspirin exacerbated respiratory disease (AERD)R01AI137174 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHLEIMER, ROBERT P · 2018 to 2022
$3.1M
NIAID NIH HHS R01 AI137174
6 · The paper itself

Abstract

backgroundCoronavirus disease 2019 (COVID-19) has caused a global pandemic. Higher expression of the virus receptor angiotensin-converting enzyme 2 (ACE2) in the nasal mucosa may be associated with high transmissibility and asymptomatic infection. In COVID-19, the elucidation of the determinants of ACE2 expression at nasal tissue level is crucial. The development of strategies to downregulate ACE2 expression in nasal epithelial cells might reduce transmission and be useful as a novel therapeutic approach.

objectiveTo verify ACE2 expression in the nasal mucosa of patients with seasonal allergic rhinitis induced by Japanese cedar pollen (SAR-JCP) and chronic rhinosinusitis with nasal polyp (CRSwNP) and to examine the effects of short-chain fatty acids (SCFAs) on ACE2 expression in airway epithelial cells.

methodsWe assessed ACE2 expression in the nasal mucosa of control subjects, patients with SAR-JCP, and those with CRSwNP using real-time polymerase chain reaction. We also quantified ACE2 gene expression in cultured airway epithelial cells.

resultsAlthough ACE2 expression was greatly increased in a few patients with SAR-JCP during the Japanese cedar pollen season, mean levels were not significantly increased. ACE2 mRNA expression was significantly decreased in nasal polyp tissue from patients with chronic rhinosinusitis compared with the expression in that from control subjects. SCFAs generated by gastrointestinal microbiota significantly reduced resting ACE2 expression in cultured airway epithelial cells. SCFAs also significantly suppressed the dsRNA-dependent upregulation of ACE2 expression in airway epithelial cells.

conclusionInflammatory endotype affects ACE2 expression in the nasal mucosa and influences susceptibility to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In particular, type 2 inflammation could downregulate ACE2 expression in the nasal mucosa and reduces susceptibility to SARS-CoV-2 in patients with CRSwNP. Although in vivo experiments are required, administration of SCFAs to the nasal cavity might be worthy of consideration as a preventative or therapeutic strategy for the early-stage COVID-19.

Indexed as

COVID-19SinusitisAngiotensin-Converting Enzyme 2HumansNasal MucosaReceptors, VirusRhinitis, Allergic, SeasonalSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2Receptors, Virusairway epithelial cellangiotensin-converting enzyme 2chronic rhinosinusitiscoronavirus disease 2019eosinophilic chronic rhinosinusitisJapanese cedar pollenseasonal allergic rhinitissevere acute respiratory syndrome coronavirus 2short-chain fatty acids

Identifiers

PMID34232770
PMCPMC11066611
OpenAlexW3179917053

What OpenQuestion holds

Textmetadata
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.