IL-17A and TNF-α as potential biomarkers for acute respiratory distress syndrome and mortality in patients with obesity and COVID-19

Med Hypotheses. 2020 Nov:144:109935. doi: 10.1016/j.mehy.2020.109935. Epub 2020 Aug 7.

Abstract

Coronavirus disease 2019 (COVID-19) was declared a pandemic and international health emergency by the World Health Organization. Patients with obesity with COVID-19 are 7 times more likely to need invasive mechanical ventilation than are patients without obesity (OR 7.36; 95% CI: 1.63-33.14, p = 0.021). Acute respiratory distress syndrome (ARDS) is one of the main causes of death related to COVID-19 and is triggered by a cytokine storm that damages the respiratory epithelium. Interleukins that cause the chronic low-grade inflammatory state of obesity, such as interleukin (IL)-1β, IL-6, monocyte chemoattractant peptide (MCP)-1, and, in particular, IL-17A and tumour necrosis factor alpha (TNF-α), also play very important roles in lung damage in ARDS. Therefore, obesity is associated with an immune state favourable to a cytokine storm. Our hypothesis is that serum concentrations of TNF-α and IL-17A are more elevated in patients with obesity and COVID-19, and consequently, they have a greater probability of developing ARDS and death. The immunobiology of IL-17A and TNF-α opens a new fascinating field of research for COVID-19.

Keywords: Acute respiratory distress syndrome; COVID-19; IL-17A; Mortality; Obesity; Tumour necrosis factor-alpha.

MeSH terms

  • Biomarkers / blood
  • COVID-19 / complications*
  • COVID-19 / immunology
  • COVID-19 / mortality
  • Cytokine Release Syndrome / etiology
  • Cytokine Release Syndrome / immunology
  • Cytokine Release Syndrome / mortality
  • Humans
  • Interleukin-17 / blood*
  • Models, Immunological
  • Obesity / complications*
  • Obesity / immunology
  • Pandemics
  • Respiratory Distress Syndrome / etiology*
  • Respiratory Distress Syndrome / immunology
  • Respiratory Distress Syndrome / mortality
  • Respiratory Mucosa / immunology
  • Respiratory Mucosa / injuries
  • Risk Factors
  • Tumor Necrosis Factor-alpha / blood*

Substances

  • Biomarkers
  • IL17A protein, human
  • Interleukin-17
  • TNF protein, human
  • Tumor Necrosis Factor-alpha