Evidence map›Paper›PMID 35708858›Full record

ArticleCellular and molecular life sciences : CMLS2022

Infection of lung megakaryocytes and platelets by SARS-CoV-2 anticipate fatal COVID-19.

Aiwei Zhu, Fernando Real, Claude Capron, Arielle R Rosenberg, Aymeric Silvin, Garett Dunsmore, Jaja Zhu, Andréa Cottoignies-Callamarte, Jean-Marc Massé, Pierre Moine and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.1field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 54 citations in OpenAlex.

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  5. Intravenous infusion of engineered megakaryocytes to produce oncolytic platelets in vivo for enhanced cancer immunotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  17. Immunological face of megakaryocytes.Frontiers of medicine · 2024
    Review
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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

24 authors at 7 institutions in 4 countries.

Aiwei Zhu *Laboratory Mucosal Entry of HIV and Mucosal Immunity, Institut Cochin, INSERM U1016, CNRS UMR8104, Université Paris Cité, 75014, Paris, France.
Fernando Real *Laboratory Mucosal Entry of HIV and Mucosal Immunity, Institut Cochin, INSERM U1016, CNRS UMR8104, Université Paris Cité, 75014, Paris, France.
Claude CapronService d'Hématologie Hôpital Ambroise Paré (AP-HP), Boulogne-Billancourt, France.
Arielle R RosenbergLaboratory Mucosal Entry of HIV and Mucosal Immunity, Institut Cochin, INSERM U1016, CNRS UMR8104, Université Paris Cité, 75014, Paris, France.
Aymeric SilvinINSERM U1015, Gustave Roussy Cancer Campus, Villejuif, France.
Garett DunsmoreINSERM U1015, Gustave Roussy Cancer Campus, Villejuif, France.
Jaja ZhuService d'Hématologie Hôpital Ambroise Paré (AP-HP), Boulogne-Billancourt, France.
Andréa Cottoignies-CallamarteLaboratory Mucosal Entry of HIV and Mucosal Immunity, Institut Cochin, INSERM U1016, CNRS UMR8104, Université Paris Cité, 75014, Paris, France.
Jean-Marc MasséElectron Microscopy platform, Institut Cochin, INSERMU1016, CNRS UMR8104, Université Paris Cité, 75014, Paris, France.
Pierre MoineFHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), RHU RECORDS (Rapid rEcognition of CORticosteroiD Resistant Or Sensitive Sepsis), Department of Intensive Care, Hôpital Raymond Poincaré (APHP), Laboratory of Infection and Inflammation - U1173, School of Medicine Simone Veil, University Versailles Saint Quentin - University Paris Saclay, INSERM, Garches, France.
Simon BessisFHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), RHU RECORDS (Rapid rEcognition of CORticosteroiD Resistant Or Sensitive Sepsis), Department of Intensive Care, Hôpital Raymond Poincaré (APHP), Laboratory of Infection and Inflammation - U1173, School of Medicine Simone Veil, University Versailles Saint Quentin - University Paris Saclay, INSERM, Garches, France.
Mathieu GodementFHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), RHU RECORDS (Rapid rEcognition of CORticosteroiD Resistant Or Sensitive Sepsis), Department of Intensive Care, Hôpital Raymond Poincaré (APHP), Laboratory of Infection and Inflammation - U1173, School of Medicine Simone Veil, University Versailles Saint Quentin - University Paris Saclay, INSERM, Garches, France.
Guillaume GeriService de Réanimation, Hôpital Ambroise Paré (AP-HP), Boulogne-Billancourt, France.
Jean-Daniel ChicheService de Réanimation, Hôpital Cochin (AP-HP), Paris, France.
Silvana ValdebenitoDepartment of Neuroscience and Cell Biology, University of Texas Medical Branch (UTMB), Galveston, TX, 77553, USA.
Sandrine BelouzardVirologie moléculaire et cellulaire des coronavirus, Centre d'infection et d'immunité de Lille, Institut Pasteur de Lille, Université de Lille, CNRS, Inserm, CHRU, 59000, Lille, France.
Jean DubuissonVirologie moléculaire et cellulaire des coronavirus, Centre d'infection et d'immunité de Lille, Institut Pasteur de Lille, Université de Lille, CNRS, Inserm, CHRU, 59000, Lille, France.
Geoffroy Lorin de la GrandmaisonService d'Anatomie et cytologie pathologiques - Médecine legale, Hôpital Raymond Poincaré (AP-HP), Garches, France.
Sylvie ChevretService de Biostatistique, Hôpital Saint Louis (AP-HP), Paris, France.
Florent GinhouxSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A(∗)STAR), Biopolis, Singapore, Singapore.
Eliseo A EugeninDepartment of Neuroscience and Cell Biology, University of Texas Medical Branch (UTMB), Galveston, TX, 77553, USA.
Djillali AnnaneFHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), RHU RECORDS (Rapid rEcognition of CORticosteroiD Resistant Or Sensitive Sepsis), Department of Intensive Care, Hôpital Raymond Poincaré (APHP), Laboratory of Infection and Inflammation - U1173, School of Medicine Simone Veil, University Versailles Saint Quentin - University Paris Saclay, INSERM, Garches, France.
Elisabeth Cramer BordéUniversité de Versailles-St Quentin en Yvelines, Versailles, France.
Morgane BomselLaboratory Mucosal Entry of HIV and Mucosal Immunity, Institut Cochin, INSERM U1016, CNRS UMR8104, Université Paris Cité, 75014, Paris, France. morgane.bomsel@inserm.fr.ORCID http://orcid.org/0000-0002-9577-7474
Centre National de la Recherche Scientifique · FRInserm · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FRAssistance Publique – Hôpitaux de Paris · FRThe University of Texas Medical Branch at Galveston · USAgency for Science, Technology and Research · SGHôpital Cochin · FR

Funding

FRM Flash COVID ANR-FRM: : ANR-20-COVI-0024
6 · The paper itself

Abstract

SARS-CoV-2, although not being a circulatory virus, spread from the respiratory tract resulting in multiorgan failures and thrombotic complications, the hallmarks of fatal COVID-19. A convergent contributor could be platelets that beyond hemostatic functions can carry infectious viruses. Here, we profiled 52 patients with severe COVID-19 and demonstrated that circulating platelets of 19 out 20 non-survivor patients contain SARS-CoV-2 in robust correlation with fatal outcome. Platelets containing SARS-CoV-2 might originate from bone marrow and lung megakaryocytes (MKs), the platelet precursors, which were found infected by SARS-CoV-2 in COVID-19 autopsies. Accordingly, MKs undergoing shortened differentiation and expressing anti-viral IFITM1 and IFITM3 RNA as a sign of viral sensing were enriched in the circulation of deadly COVID-19. Infected MKs reach the lung concomitant with a specific MK-related cytokine storm rich in VEGF, PDGF and inflammatory molecules, anticipating fatal outcome. Lung macrophages capture SARS-CoV-2-containing platelets in vivo. The virus contained by platelets is infectious as capture of platelets carrying SARS-CoV-2 propagates infection to macrophages in vitro, in a process blocked by an anti-GPIIbIIIa drug. Altogether, platelets containing infectious SARS-CoV-2  alter COVID-19 pathogenesis and provide a powerful fatality marker. Clinical targeting of platelets might prevent viral spread, thrombus formation and exacerbated inflammation at once and increase survival in COVID-19.

Indexed as

COVID-19ThrombosisBlood PlateletsHumansLungMegakaryocytesMembrane ProteinsRNA-Binding ProteinsSARS-CoV-2IFITM3 protein, humanMembrane ProteinsRNA-Binding ProteinsCOVID-19LungMacrophagesMegakaryocytesPlateletsSARS-CoV-2

Identifiers

PMID35708858
PMCPMC9201269
OpenAlexW4282981825

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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 OpenQuestion graph.