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

EMBO Mol Med. 2020 Dec 7;12(12):e13001. doi: 10.15252/emmm.202013001. Epub 2020 Nov 5.

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.

Keywords: COVID-19; OXPHOS; inhibitory checkpoints; mitochondria; monocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • COVID-19 / pathology*
  • COVID-19 / virology
  • Case-Control Studies
  • Chemokines / blood
  • Cytokines / blood
  • Energy Metabolism / physiology*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mitochondria / metabolism*
  • Mitochondria / ultrastructure
  • Monocytes / cytology
  • Monocytes / metabolism*
  • Programmed Cell Death 1 Receptor / genetics
  • Programmed Cell Death 1 Receptor / metabolism
  • SARS-CoV-2 / isolation & purification

Substances

  • Chemokines
  • Cytokines
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor