Evidence map›Paper›PMID 40593263›Full record

ArticleScientific reports2025

CXCL10-dependent epithelial-vascular cross-talk for endothelial activation following SARS-CoV-2 infection.

Laura Chaillot, Marie-Lise Blondot, Patricia Recordon-Pinson, Isabelle Pellegrin, Andrea Boizard-Moracchini, Myroslava Sliusar, Teo Leboucq, Nadege Pujol, Marie-Line Andreola, Fabrice Bonnet and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Laura ChaillotBRIC INSERM U1312, Université de Bordeaux, Pessac, 33615, France.
Marie-Lise BlondotMFP Laboratory, UMR5234, CNRS Université de Bordeaux, Bordeaux, France.
Patricia Recordon-PinsonMFP Laboratory, UMR5234, CNRS Université de Bordeaux, Bordeaux, France.
Isabelle PellegrinLaboratoire d'Immunologie-Immunogenetique, Centre de Ressources Biologiques Bordeaux Biothèques Santé (CRB-BBS), CHU de Bordeaux, Bordeaux, France.
Andrea Boizard-MoracchiniLaboratoire d'Immunologie-Immunogenetique, Centre de Ressources Biologiques Bordeaux Biothèques Santé (CRB-BBS), CHU de Bordeaux, Bordeaux, France.
Myroslava SliusarBRIC INSERM U1312, Université de Bordeaux, Pessac, 33615, France.
Teo LeboucqBRIC INSERM U1312, Université de Bordeaux, Pessac, 33615, France.
Nadege PujolBRIC INSERM U1312, Université de Bordeaux, Pessac, 33615, France.
Marie-Line AndreolaMFP Laboratory, UMR5234, CNRS Université de Bordeaux, Bordeaux, France.
Fabrice BonnetService de Médecine Interne et Maladies Infectieuses, CHU de Bordeaux, Hôpital Saint-André, Université de Bordeaux, Bordeaux Population Health, INSERM U1219, Bordeaux, 33000, France.
Gaelle RecherLP2N, Laboratoire Photonique Numérique et Nanosciences, Univ. Bordeaux, Talence, 33400, France.
Laetitia AndriqueVoxCell 3D Facility UAR TBMcore CNRS, 3427-INSERMUS05, Université de Bordeaux, Bordeaux, France.
Pierre NassoyLP2N, Laboratoire Photonique Numérique et Nanosciences, Univ. Bordeaux, Talence, 33400, France.
Thomas MathivetBRIC INSERM U1312, Université de Bordeaux, Pessac, 33615, France. Thomas.mathivet@inserm.fr.
Andreas BikfalviBRIC INSERM U1312, Université de Bordeaux, Pessac, 33615, France. andreas.bikfalvi@u-bordeaux.fr.

Funding

Agence Nationale de la Recherche IVEONFondation pour la Recherche Médicale VascCovUniversité de Bordeaux Spark-Covid project
6 · The paper itself

Abstract

The blood vessel network is heavily impacted by SARS-CoV-2 infection. How SARS-CoV-2 contributes to vascular inflammation and whether epithelio-endothelial cross-talk is involved remain unclear. We investigated in detail the interaction between SARS-CoV-2 and the vasculature using 2D and 3D vesseloid in vitro models. We first assessed whether SARS-CoV-2 is able to directly infect endothelial cells. In the absence of ACE2 in endothelial cells, no productive infection was detected. Low uptake of viral particles by ACE2-overexpressing endothelial cells was observed without efficient viral production. Thus, the indirect effect of SARS-CoV-2 infection may involve epithelio-endothelial cell cross-talk. After infection of the epithelial cells, a significant inflammatory response was detected in the endothelial cells. CXCL10 was the most highly expressed proinflammatory cytokine involved in this intercellular communication, and its function was subsequently explored. Finally, the clinical relevance of our findings was confirmed in two patient cohorts.

Indexed as

Chemokine CXCL10COVID-19Endothelial CellsEpithelial CellsSARS-CoV-2Angiotensin-Converting Enzyme 2Cell CommunicationEndothelium, VascularHumansHuman Umbilical Vein Endothelial CellsACE2 protein, humanAngiotensin-Converting Enzyme 2Chemokine CXCL10CXCL10 protein, humanChemokinesCXCL10EndotheliumSARS-CoV-2

Identifiers

PMID40593263
PMCPMC12218331

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.