Evidence map›Paper›PMID 39172744›Full record

ArticlePLoS pathogens2024

The assembly of neutrophil inflammasomes during COVID-19 is mediated by type I interferons.

Luz E Cabrera, Suvi T Jokiranta, Sanna Mäki, Simo Miettinen, Ravi Kant, Lauri Kareinen, Tarja Sironen, Jukka-Pekka Pietilä, Anu Kantele, Eliisa Kekäläinen and 5 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Observational
  2. Review
  3. Article
  4. Frontiers in immunology · 2025
    Article
  5. Article
  6. 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

15 authors.

Luz E CabreraViral Zoonosis Research Unit, Medicum, Department of Virology, University of Helsinki, Helsinki, Finland.ORCID 0000-0001-9437-1010
Suvi T JokirantaDepartment of Bacteriology and Immunology, University of Helsinki, Helsinki, Finland.
Sanna MäkiViral Zoonosis Research Unit, Medicum, Department of Virology, University of Helsinki, Helsinki, Finland.
Simo MiettinenViral Zoonosis Research Unit, Medicum, Department of Virology, University of Helsinki, Helsinki, Finland.
Ravi KantViral Zoonosis Research Unit, Medicum, Department of Virology, University of Helsinki, Helsinki, Finland.
Lauri KareinenViral Zoonosis Research Unit, Medicum, Department of Virology, University of Helsinki, Helsinki, Finland.
Tarja SironenViral Zoonosis Research Unit, Medicum, Department of Virology, University of Helsinki, Helsinki, Finland.
Jukka-Pekka PietiläHuman Microbiome Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Anu KanteleHuman Microbiome Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Eliisa KekäläinenDepartment of Bacteriology and Immunology, University of Helsinki, Helsinki, Finland.
Hanna LindgrenInstitute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.
Pirkko MattilaInstitute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.
Anja KiparDepartment of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
Olli VapalahtiViral Zoonosis Research Unit, Medicum, Department of Virology, University of Helsinki, Helsinki, Finland.
Tomas StrandinViral Zoonosis Research Unit, Medicum, Department of Virology, University of Helsinki, Helsinki, Finland.

Funding

Academy of Finland 321809EU Horizon 2020 programme VEO 874735Finnish governmental subsidy for Health Science Research TYH 2021315Helsinki University Hospital TYH 2021343
6 · The paper itself

Abstract

The severity of COVID-19 is linked to excessive inflammation. Neutrophils represent a critical arm of the innate immune response and are major mediators of inflammation, but their role in COVID-19 pathophysiology remains poorly understood. We conducted transcriptomic profiling of neutrophils obtained from patients with mild and severe COVID-19, as well as from SARS-CoV-2 infected mice, in comparison to non-infected healthy controls. In addition, we investigated the inflammasome formation potential in neutrophils from patients and mice upon SARS-CoV-2 infection. Transcriptomic analysis of polymorphonuclear cells (PMNs), consisting mainly of mature neutrophils, revealed a striking type I interferon (IFN-I) gene signature in severe COVID-19 patients, contrasting with mild COVID-19 and healthy controls. Notably, low-density granulocytes (LDGs) from severe COVID-19 patients exhibited an immature neutrophil phenotype and lacked this IFN-I signature. Moreover, PMNs from severe COVID-19 patients showed heightened nigericin-induced caspase1 activation, but reduced responsiveness to exogenous inflammasome priming. Furthermore, IFN-I emerged as a priming stimulus for neutrophil inflammasomes. These findings suggest a potential role for neutrophil inflammasomes in driving inflammation during severe COVID-19. Altogether, these findings open promising avenues for targeted therapeutic interventions to mitigate the pathological processes associated with the disease.

Indexed as

COVID-19InflammasomesInterferon Type INeutrophilsSARS-CoV-2AdultAnimalsFemaleHumansImmunity, InnateMaleMiceMice, Inbred C57BLMiddle AgedInflammasomesInterferon Type I

Identifiers

PMID39172744
PMCPMC11340896

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.