Evidence mapPaperPMID 41748828Full record

ArticleScientific reports2026

Serum CD73 activity as a biomarker of hypoxemia in COVID-19 patients.

Pierrick Le Borgne, Pascal Bilbault, Raphael Clere-Jehl, Julie Favre, François Lefebvre, Geneviève Ubeaud-Séquier, Fatiha El Ghazouani, Julien Demiselle, Florence Toti, Ferhat Meziani and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 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
0cells of the map it votes in
0citing 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

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

11 authors.

Pierrick Le BorgneUniversité de Strasbourg, INSERM, Regenerative NanoMedicine (RNM), UMR 1260, CRBS, 1 rue Eugène Boeckel, Strasbourg, 67000, France. pierrick.le-borgne@chru-strasbourg.fr.
Pascal BilbaultUniversité de Strasbourg, INSERM, Regenerative NanoMedicine (RNM), UMR 1260, CRBS, 1 rue Eugène Boeckel, Strasbourg, 67000, France.
Raphael Clere-JehlEmergency Department, Hôpitaux Universitaires de Strasbourg, 1 Avenue Molière, Strasbourg cedex, F-67091, France.
Julie FavreBiotechnologie et Signalisation Cellulaire, CNRS UMR 7242, Université de Strasbourg, University of Strasbourg, Strasbourg, France.
François LefebvreDepartment of Public Health, University Hospital of Strasbourg, Strasbourg, France.
Geneviève Ubeaud-SéquierDepartment of Pharmacy, Strasbourg University Hospital, Strasbourg, France.
Fatiha El GhazouaniUniversité de Strasbourg, INSERM, Regenerative NanoMedicine (RNM), UMR 1260, CRBS, 1 rue Eugène Boeckel, Strasbourg, 67000, France.
Julien DemiselleUniversité de Strasbourg, INSERM, Regenerative NanoMedicine (RNM), UMR 1260, CRBS, 1 rue Eugène Boeckel, Strasbourg, 67000, France.
Florence TotiUniversité de Strasbourg, INSERM, Regenerative NanoMedicine (RNM), UMR 1260, CRBS, 1 rue Eugène Boeckel, Strasbourg, 67000, France.
Ferhat MezianiUniversité de Strasbourg, INSERM, Regenerative NanoMedicine (RNM), UMR 1260, CRBS, 1 rue Eugène Boeckel, Strasbourg, 67000, France.
Gilles KauffensteinUniversité de Strasbourg, INSERM, Regenerative NanoMedicine (RNM), UMR 1260, CRBS, 1 rue Eugène Boeckel, Strasbourg, 67000, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ectonucleotidases regulate extracellular purine signaling and play a key role in inflammation and thrombosis, two major components of COVID-19 pathophysiology. We investigated the enzymatic activities of CD39 (NTPDase1) and CD73 (ecto-5’-nucleotidase) as potential biomarkers of disease severity. Patients with RT-PCR-confirmed COVID-19 were enrolled between August 1st, 2020, and August 1st, 2021, and stratified into mild to moderate (MM, n = 55) or severe to critical (SC, n = 30) groups according to WHO criteria. Serum samples were collected on days 1, 3, and 7 following Emergency Department (ED) admission. CD39 and CD73 activities were measured by HPLC using etheno-fluorescent nucleotide substrates and compared to healthy volunteers (HV, n = 30) matched for age and sex. Serum CD73 activity was significantly elevated in COVID-19 patients compared to HV (MM: 76 ± 9.4; SC: 99 ± 21 vs. HV: 25 ± 2.7 pmol/min/µL; p < 0.0001), particularly in patients requiring ≥ 6 L/min oxygen (p = 0.005) or with a respiratory rate > 20/min (p = 0.02). CD73 activity remained elevated throughout hospitalization. Conversely, febrile patients (≥ 38 °C) and those with CRP ≥ 100 mg/L exhibited significantly lower CD73 activity (p = 0.023 and p = 0.004, respectively). CD39 activity was undetectable in 28.2% of patients and showed no association with disease severity or outcome. The lowest CD73 levels were observed in patients requiring oxygen therapy for ≥ 30 days and in those who died before day 7. Serum CD73 activity is associated with hypoxemia and oxygen requirements upon ED admission. Conversely, low CD73 activity reflects a hyperinflammatory state and worse outcomes, supporting its potential use in biomarker-based risk stratification for COVID-19.

Indexed as

5'-NucleotidaseCOVID-19HypoxiaAdultAgedAntigens, CDApyraseBiomarkersFemaleGPI-Linked ProteinsHumansMaleMiddle AgedSARS-CoV-2Severity of Illness Index5'-NucleotidaseAntigens, CDApyraseBiomarkersGPI-Linked ProteinsNT5E protein, humanCD73COVID-19Ecto 5’-nucleotidaseEctonucleotidasesSARS-CoV-2

Identifiers

PMID41748828
PMCPMC13043897

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.