Evidence mapPaperPMID 41280914Full record

ArticleFrontiers in immunology2025

Neutrophil gene expression in COVID-19 patients with acute respiratory distress syndrome.

Hiroshi Ito, Masakazu Ishikawa, Jumpei Yoshimura, Yuchen Liu, Shuhei Sakakibara, Fuminori Sugihara, Hisatake Matsumoto, Haruhiko Hirata, Hiroshi Ogura, Jun Oda and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
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

1 citing paper in PubMed.

  1. Review
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

11 authors.

Hiroshi Ito *Department of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Suita, Osaka,, Japan.
Masakazu Ishikawa *Laboratory for Human Immunology (Single Cell Genomics), WPI (World Premier International Research Center Initiative) Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan.
Jumpei Yoshimura *Department of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Suita, Osaka,, Japan.
Yuchen LiuLaboratory for Human Immunology (Single Cell Genomics), WPI (World Premier International Research Center Initiative) Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan.
Shuhei SakakibaraLaboratory of Immune Regulation, Immunology Frontier Research Center, Osaka University, Suita, Japan.
Fuminori SugiharaCore Instrumentation Facility, Immunology Frontier Research Center and Research Institute for Microbial Disease, Osaka University, Suita, Osaka, Japan.
Hisatake MatsumotoDepartment of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Suita, Osaka,, Japan.
Haruhiko HirataDepartment of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Hiroshi OguraDepartment of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Suita, Osaka,, Japan.
Jun OdaDepartment of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Suita, Osaka,, Japan.
Daisuke OkuzakiLaboratory for Human Immunology (Single Cell Genomics), WPI (World Premier International Research Center Initiative) Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Although an increase in neutrophil count has been observed in patients with coronavirus disease 2019 (COVID-19), the relationship between the systemic neutrophil transcriptome and clinical course of COVID-19 remains unclear. Hence, we examined the relationship between the clinical course and RNA sequencing analysis results in COVID-19 patients. Methods: Peripheral blood samples were obtained from 28 patients with COVID-19-associated ARDS and 16 healthy controls. Bulk RNA sequencing was performed, and clustering analysis was used to explore relationships between gene expression and clinical characteristics. In a separate cohort, neutrophils were isolated from the peripheral blood of five COVID-19 patients with ARDS for single-cell RNA sequencing to further characterize the neutrophil subpopulations. Results: In bulk RNA sequencing analysis, COVID-19 patients with ARDS had elevated gene expression associated with neutrophils compared with healthy controls.Clustering analysis revealed no differences in the clinical characteristics of COVID-19 patients with ARDS. In the single-cell RNA sequencing analysis, clustering analysis showed that the patients were divided into two groups: those who could be weaned from the ventilator within 28 days and those who could not be weaned. Conclusion: These findings indicate that differences in neutrophil gene expression may have important clinical implications. This study may support the exploratory identification of genomic factors, such as neutrophil gene expression, that are relevant to clinical parameters.

Indexed as

COVID-19NeutrophilsRespiratory Distress SyndromeSARS-CoV-2AdultAgedFemaleHumansMaleMiddle AgedSequence Analysis, RNASingle-Cell AnalysisTranscriptomeacute respiratory distress syndromecoronavirus disease 2019 (COVID-19)gene expressionneutrophilsingle-cell RNA sequencing

Identifiers

PMID41280914
PMCPMC12631193

What Socratic holds

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Registered trials

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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 Socratic graph.