Evidence map›Paper›PMID 35842415›Full record

ArticleCell death discovery2022

Platelet proteome reveals features of cell death, antiviral response and viral replication in covid-19.

Monique R O Trugilho, Isaclaudia G Azevedo-Quintanilha, João S M Gesto, Emilly Caroline S Moraes, Samuel C Mandacaru, Mariana M Campos, Douglas M Oliveira, Suelen S G Dias, Viviane A Bastos, Marlon D M Santos and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Molecular mechanisms of SARS-CoV-2 entry: implications for biomedical strategies.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Nutrients · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Alterations in platelet proteome signature and impaired platelet integrin αJournal of thrombosis and haemostasis : JTH · 2023
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Frontiers in microbiology · 2022
    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

17 authors at 4 institutions in 1 country.

Monique R O Trugilho *Center for Technological Development in Health, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil. monique.trugilho@fiocruz.br.ORCID http://orcid.org/0000-0001-9240-9978
Isaclaudia G Azevedo-Quintanilha *Laboratory of Immunopharmacology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0003-1826-4285
João S M GestoCenter for Technological Development in Health, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Emilly Caroline S MoraesLaboratory of Toxinology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0001-8634-2498
Samuel C MandacaruCenter for Technological Development in Health, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0001-9255-1958
Mariana M CamposLaboratory of Immunopharmacology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0001-9574-4026
Douglas M OliveiraLaboratory of Immunopharmacology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Suelen S G DiasLaboratory of Immunopharmacology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0002-3104-0983
Viviane A BastosLaboratory of Toxinology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0001-5543-4058
Marlon D M SantosLaboratory for Structural and Computational Proteomics, Carlos Chagas Institute, Oswaldo Cruz Foundation, Curitiba, Brazil.ORCID http://orcid.org/0000-0002-1178-1266
Paulo C CarvalhoLaboratory for Structural and Computational Proteomics, Carlos Chagas Institute, Oswaldo Cruz Foundation, Curitiba, Brazil.ORCID http://orcid.org/0000-0001-6530-3350
Richard H ValenteLaboratory of Toxinology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0002-6562-7571
Eugenio D HottzLaboratory of Immunothrombosis, Department of Biochemistry, Federal University of Juiz de Fora, Juiz de Fora, MG, Brazil.ORCID http://orcid.org/0000-0002-2201-1742
Fernando A BozzaNational Institute of Infectious Disease Evandro Chagas, Oswaldo Cruz Foundation, and D'Or Institute for Research and Education, Rio de Janeiro, Brazil.
Thiago Moreno L SouzaCenter for Technological Development in Health, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Jonas PeralesLaboratory of Toxinology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0002-0157-1783
Patrícia T BozzaLaboratory of Immunopharmacology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil. pbozza@ioc.fiocruz.br.ORCID http://orcid.org/0000-0001-8349-9529
Fundação Oswaldo Cruz · BRFundação Carlos Chagas · BRD’Or Institute for Research and Education · BRUniversidade Federal de Juiz de Fora · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) has affected over 400 million people worldwide, leading to 6 million deaths. Among the complex symptomatology of COVID-19, hypercoagulation and thrombosis have been described to directly contribute to lethality, pointing out platelets as an important SARS-CoV-2 target. In this work, we explored the platelet proteome of COVID-19 patients through a label-free shotgun proteomics approach to identify platelet responses to infection, as well as validation experiments in a larger patient cohort. Exclusively detected proteins (EPs) and differentially expressed proteins (DEPs) were identified in the proteomic dataset and thus classified into biological processes to map pathways correlated with pathogenesis. Significant changes in the expression of proteins related to platelet activation, cell death, and antiviral response through interferon type-I were found in all patients. Since the outcome of COVID-19 varies highly among individuals, we also performed a cross-comparison of proteins found in survivors and nonsurvivors. Proteins belonging to the translation pathway were strongly highlighted in the nonsurvivor group. Moreover, the SARS-CoV-2 genome was fully sequenced in platelets from five patients, indicating viral internalization and preprocessing, with CD147 as a potential entry route. In summary, platelets play a significant role in COVID-19 pathogenesis via platelet activation, antiviral response, and disease severity.

Identifiers

PMID35842415
PMCPMC9287722
OpenAlexW4285587737

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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.