DAMPening COVID-19 Severity by Attenuating Danger Signals

Front Immunol. 2021 Aug 12:12:720192. doi: 10.3389/fimmu.2021.720192. eCollection 2021.

Abstract

COVID-19 might lead to multi-organ failure and, in some cases, to death. The COVID-19 severity is associated with a "cytokine storm." Danger-associated molecular patterns (DAMPs) are proinflammatory molecules that can activate pattern recognition receptors, such as toll-like receptors (TLRs). DAMPs and TLRs have not received much attention in COVID-19 but can explain some of the gender-, weight- and age-dependent effects. In females and males, TLRs are differentially expressed, likely contributing to higher COVID-19 severity in males. DAMPs and cytokines associated with COVID-19 mortality are elevated in obese and elderly individuals, which might explain the higher risk for severer COVID-19 in these groups. Adenosine signaling inhibits the TLR/NF-κB pathway and, through this, decreases inflammation and DAMPs' effects. As vaccines will not be effective in all susceptible individuals and as new vaccine-resistant SARS-CoV-2 mutants might develop, it remains mandatory to find means to dampen COVID-19 disease severity, especially in high-risk groups. We propose that the regulation of DAMPs via adenosine signaling enhancement might be an effective way to lower the severity of COVID-19 and prevent multiple organ failure in the absence of severe side effects.

Keywords: COVID-19; DAMPs; SARS-CoV2; TLRs; adenosine; cytokine storm.

Publication types

  • Review

MeSH terms

  • Adenosine / metabolism
  • Alarmins / antagonists & inhibitors
  • Alarmins / immunology*
  • Animals
  • COVID-19 / complications
  • COVID-19 / immunology
  • COVID-19 / physiopathology*
  • COVID-19 / therapy
  • Humans
  • Inflammation / prevention & control
  • Inflammation Mediators / antagonists & inhibitors
  • Inflammation Mediators / immunology*
  • Multiple Organ Failure / etiology
  • Multiple Organ Failure / prevention & control
  • Patient Acuity
  • Signal Transduction
  • Toll-Like Receptors / antagonists & inhibitors
  • Toll-Like Receptors / immunology

Substances

  • Alarmins
  • Inflammation Mediators
  • Toll-Like Receptors
  • Adenosine