Evidence map›Paper›PMID 37104043›Full record

ArticleThe Journal of clinical investigation2023

C5aR1 signaling triggers lung immunopathology in COVID-19 through neutrophil extracellular traps.

Bruna M Silva, Giovanni F Gomes, Flavio P Veras, Seppe Cambier, Gabriel Vl Silva, Andreza U Quadros, Diego B Caetité, Daniele C Nascimento, Camilla M Silva, Juliana C Silva and 34 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.2field-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

25 citing papers in PubMed, 27 citations in OpenAlex.

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  10. Cytosolic proliferating cell nuclear antigen (PCNA) orchestrates neutrophil hyperactivation in COVID-19.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Review
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  18. Neutrophil extracellular traps in homeostasis and disease.Signal transduction and targeted therapy · 2024
    Review
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  20. 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

44 authors at 7 institutions in 6 countries.

Bruna M SilvaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Giovanni F GomesCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Flavio P VerasCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Seppe CambierLaboratory of Molecular Immunology, Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium.
Gabriel Vl SilvaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Andreza U QuadrosCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Diego B CaetitéCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Daniele C NascimentoCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Camilla M SilvaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Juliana C SilvaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Samara DamascenoCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Ayda H SchneiderCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Fabio BerettaLaboratory of Molecular Immunology, Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium.
Sabrina S BatahDepartment of Pathology and Legal Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Icaro Ms CastroHospital Israelita Albert Einstein, São Paulo, Brazil.
Isadora M PaivaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Tamara RodriguesCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Ana SalinaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Ronaldo MartinsDepartment of Cell and Molecular Biology.
Guilherme Cm CebinelliCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Naira L BiboCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Daniel M JorgeDepartment of Cell and Molecular Biology.
Helder I NakayaHospital Israelita Albert Einstein, São Paulo, Brazil.
Dario S ZamboniCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Luiz O LeiriaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Alexandre T FabroDepartment of Pathology and Legal Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
José C Alves-FilhoCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Eurico ArrudaDepartment of Cell and Molecular Biology.
Paulo Louzada-JuniorCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Renê D OliveiraCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Larissa D CunhaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Pierre Van MolLaboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism, and.
Lore VanderbekeLaboratory for Clinical Infectious and Inflammatory Disorders, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Simon FeysLaboratory for Clinical Infectious and Inflammatory Disorders, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Els WautersLaboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases and Metabolism, and.
Laura BrandoliniR&D Department, Dompé Farmaceutici s.p.a., via Campo di Pile, L'Aquila, Italy.
Andrea AraminiR&D Department, Dompé Farmaceutici s.p.a., via Campo di Pile, L'Aquila, Italy.
Fernando Q CunhaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Jörg KöhlDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Marcello AllegrettiR&D Department, Dompé Farmaceutici s.p.a., via Campo di Pile, L'Aquila, Italy.
Diether LambrechtsLaboratory of Translational Genetics, Department of Human Genetics, VIB-KU Leuven, Leuven, Belgium.
Joost WautersLaboratory for Clinical Infectious and Inflammatory Disorders, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Paul ProostLaboratory of Molecular Immunology, Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium.
Thiago M CunhaCenter for Research in Inflammatory Diseases (CRID), Department of Pharmacology, and.
Universidade de São Paulo · BRInstitute of Molecular and Cell Biology · RUKU Leuven · BEDompé (Italy) · ITRega Institute for Medical Research · BEHospital Israelita Albert Einstein · BRCincinnati Children's Hospital Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with severe COVID-19 develop acute respiratory distress syndrome (ARDS) that may progress to cytokine storm syndrome, organ dysfunction, and death. Considering that complement component 5a (C5a), through its cellular receptor C5aR1, has potent proinflammatory actions and plays immunopathological roles in inflammatory diseases, we investigated whether the C5a/C5aR1 pathway could be involved in COVID-19 pathophysiology. C5a/C5aR1 signaling increased locally in the lung, especially in neutrophils of critically ill patients with COVID-19 compared with patients with influenza infection, as well as in the lung tissue of K18-hACE2 Tg mice (Tg mice) infected with SARS-CoV-2. Genetic and pharmacological inhibition of C5aR1 signaling ameliorated lung immunopathology in Tg-infected mice. Mechanistically, we found that C5aR1 signaling drives neutrophil extracellular traps-dependent (NETs-dependent) immunopathology. These data confirm the immunopathological role of C5a/C5aR1 signaling in COVID-19 and indicate that antagonists of C5aR1 could be useful for COVID-19 treatment.

Indexed as

COVID-19Extracellular TrapsAnimalsComplement C5aCOVID-19 Drug TreatmentHumansLungMiceSARS-CoV-2Complement C5aComplementCOVID-19InflammationInnate immunityMolecular pathology

Identifiers

PMID37104043
PMCPMC10266787
OpenAlexW4367174308

What Socratic holds

Textmetadata
LicenceCC BY
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.