Evidence map›Paper›PMID 33078545›Full record

ArticleEMBO molecular medicine2020

Altered bioenergetics and mitochondrial dysfunction of monocytes in patients with COVID-19 pneumonia.

Lara Gibellini, Sara De Biasi, Annamaria Paolini, Rebecca Borella, Federica Boraldi, Marco Mattioli, Domenico Lo Tartaro, Lucia Fidanza, Alfredo Caro-Maldonado, Marianna Meschiari and 10 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed, 2 pooled it
14.1field-weighted citation impact, top 1% 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

124 citing papers in PubMed, 2 syntheses or guidelines pooled it, 212 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Review
  8. Observational
  9. Article
  10. Article
  11. Review
  12. Monocyte Involvement in the Pathogenesis of Myeloproliferative Neoplasms.International journal of molecular sciences · 2025
    Review
  13. Review
  14. Article
  15. T-lymphocytes suppression by CD14Journal of translational medicine · 2025
    Article
  16. Article
  17. Article
  18. Observational
  19. Article
  20. Article

64 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 4 institutions in 3 countries.

Lara GibelliniDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0002-4268-6552
Sara De BiasiDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0002-3217-9821
Annamaria PaoliniDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Rebecca BorellaDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Federica BoraldiDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Marco MattioliDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Domenico Lo TartaroDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Lucia FidanzaDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Alfredo Caro-MaldonadoAgilent Technologies, Madrid, Spain.
Marianna MeschiariInfectious Diseases Clinics, AOU Policlinico and University of Modena and Reggio Emilia, Modena, Italy.
Vittorio IadiserniaInfectious Diseases Clinics, AOU Policlinico and University of Modena and Reggio Emilia, Modena, Italy.
Erica BaccaInfectious Diseases Clinics, AOU Policlinico and University of Modena and Reggio Emilia, Modena, Italy.
Giovanni RivaDepartment of Laboratory Medicine and Pathology, AUSL/AOU Policlinico, Modena, Italy.
Luca CicchettiLabospace srl, Milan, Italy.
Daniela QuaglinoDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Giovanni GuaraldiInfectious Diseases Clinics, AOU Policlinico and University of Modena and Reggio Emilia, Modena, Italy.
Stefano BusaniDepartment of Anesthesia and Intensive Care, AOU Policlinico and University of Modena and Reggio Emilia, Modena, Italy.
Massimo GirardisDepartment of Anesthesia and Intensive Care, AOU Policlinico and University of Modena and Reggio Emilia, Modena, Italy.
Cristina MussiniInfectious Diseases Clinics, AOU Policlinico and University of Modena and Reggio Emilia, Modena, Italy.
Andrea CossarizzaDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
University of Modena and Reggio Emilia · ITAgilent Technologies (United States) · USAzienda Ospedaliero-Universitaria di Modena · ITClinipace (Italy) · IT

Funding

Ministry of Health, Italy | Ministero della Salute
6 · The paper itself

Abstract

In patients infected by SARS-CoV-2 who experience an exaggerated inflammation leading to pneumonia, monocytes likely play a major role but have received poor attention. Thus, we analyzed peripheral blood monocytes from patients with COVID-19 pneumonia and found that these cells show signs of altered bioenergetics and mitochondrial dysfunction, had a reduced basal and maximal respiration, reduced spare respiratory capacity, and decreased proton leak. Basal extracellular acidification rate was also diminished, suggesting reduced capability to perform aerobic glycolysis. Although COVID-19 monocytes had a reduced ability to perform oxidative burst, they were still capable of producing TNF and IFN-γ in vitro. A significantly high amount of monocytes had depolarized mitochondria and abnormal mitochondrial ultrastructure. A redistribution of monocyte subsets, with a significant expansion of intermediate/pro-inflammatory cells, and high amounts of immature monocytes were found, along with a concomitant compression of classical monocytes, and an increased expression of inhibitory checkpoints like PD-1/PD-L1. High plasma levels of several inflammatory cytokines and chemokines, including GM-CSF, IL-18, CCL2, CXCL10, and osteopontin, finally confirm the importance of monocytes in COVID-19 immunopathogenesis.

Indexed as

AdultAgedAged, 80 and overCase-Control StudiesChemokinesCOVID-19CytokinesEnergy MetabolismFemaleHumansMaleMiddle AgedMitochondriaMonocytesProgrammed Cell Death 1 ReceptorSARS-CoV-2ChemokinesCytokinesPDCD1 protein, humanProgrammed Cell Death 1 ReceptorCOVID-19inhibitory checkpointsmitochondriamonocytesOXPHOS

Identifiers

PMID33078545
PMCPMC7645870
OpenAlexW3093107571

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.