Emerging role of IL-6 and NLRP3 inflammasome as potential therapeutic targets to combat COVID-19: Role of lncRNAs in cytokine storm modulation

Life Sci. 2020 Sep 15:257:118114. doi: 10.1016/j.lfs.2020.118114. Epub 2020 Jul 18.

Abstract

The world has witnessed a high morbidity and mortality caused by SARS-CoV-2, and global death toll is still rising. Exaggerated inflammatory responses are thought to be more responsible for infiltrated immune cells accumulation, organ damage especially lung, dyspnea, and respiratory failure rather than direct effect of viral replication. IL-6 and NLRP3 inflammasome are the major immune components in immune responses stimulation upon pathogen infection. It's noteworthy that the function and expression of these components are remarkably influenced by non-coding RNAs including long non-coding RNAs. Given the potential role of these components in organ damage and pathological manifestations of patients infected with COVID-19, their blockage might be a hopeful and promising treatment strategy. Notably, more study on long non-coding RNAs involved in inflammatory responses could elevate the efficacy of anti-inflammatory therapy. In this review we discuss the potential impact of IL-6 and NLRP3 inflammasome blocker drugs on inflammatory responses, viral clearance, and pathological and clinical manifestations. Collectively, anti-inflammatory strategy might pave the way to diminish clinical and pathological manifestations and thereby discharging patients infected with COVID-19 from hospital.

Keywords: COVID-19; Cytokine release syndrome; Drug; Inflammasome; Inflammation; SARS-CoV-2.

Publication types

  • Review

MeSH terms

  • Anti-Inflammatory Agents / pharmacology
  • Betacoronavirus / genetics*
  • Betacoronavirus / immunology
  • Betacoronavirus / metabolism
  • COVID-19
  • Coronavirus Infections / immunology*
  • Coronavirus Infections / metabolism
  • Cytokines / genetics
  • Cytokines / immunology
  • Humans
  • Inflammasomes / immunology
  • Inflammation / immunology
  • Interleukin-6 / immunology*
  • Interleukin-6 / metabolism
  • Interleukin-6 / pharmacology
  • NLR Family, Pyrin Domain-Containing 3 Protein / immunology
  • Pandemics
  • Pneumonia, Viral / immunology*
  • Pneumonia, Viral / metabolism
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / physiology*
  • SARS-CoV-2

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Inflammasomes
  • Interleukin-6
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • NLRP3 protein, human
  • RNA, Long Noncoding