Periodontitis-Derived Dark-NETs in Severe Covid-19

Front Immunol. 2022 Apr 12:13:872695. doi: 10.3389/fimmu.2022.872695. eCollection 2022.

Abstract

The frequent severe COVID-19 course in patients with periodontitis suggests a link of the aetiopathogenesis of both diseases. The formation of intravascular neutrophil extracellular traps (NETs) is crucial to the pathogenesis of severe COVID-19. Periodontitis is characterised by an increased level of circulating NETs, a propensity for increased NET formation, delayed NET clearance and low-grade endotoxemia (LGE). The latter has an enormous impact on innate immunity and susceptibility to infection with SARS-CoV-2. LPS binds the SARS-CoV-2 spike protein and this complex, which is more active than unbound LPS, precipitates massive NET formation. Thus, circulating NET formation is the common denominator in both COVID-19 and periodontitis and other diseases with low-grade endotoxemia like diabetes, obesity and cardiovascular diseases (CVD) also increase the risk to develop severe COVID-19. Here we discuss the role of propensity for increased NET formation, DNase I deficiency and low-grade endotoxaemia in periodontitis as aggravating factors for the severe course of COVID-19 and possible strategies for the diminution of increased levels of circulating periodontitis-derived NETs in COVID-19 with periodontitis comorbidity.

Keywords: NET hyper-responsiveness; NET-induced damage; dysregulated immunity; inhibition of NET formation; neutrophil hyper-responsiveness; trained immunity.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • COVID-19*
  • Endotoxemia* / metabolism
  • Extracellular Traps*
  • Humans
  • Lipopolysaccharides / metabolism
  • Neutrophils
  • Periodontitis* / pathology
  • SARS-CoV-2
  • Spike Glycoprotein, Coronavirus

Substances

  • Lipopolysaccharides
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2