SARS-CoV-2 Infection Triggers Auto-Immune Response in ARDS

Front Immunol. 2022 Jan 28:13:732197. doi: 10.3389/fimmu.2022.732197. eCollection 2022.

Abstract

Acute respiratory distress syndrome (ARDS) is a severe pulmonary disease, which is one of the major complications in COVID-19 patients. Dysregulation of the immune system and imbalances in cytokine release and immune cell activation are involved in SARS-CoV-2 infection. Here, the inflammatory, antigen, and auto-immune profile of patients presenting COVID-19-associated severe ARDS has been analyzed using functional proteomics approaches. Both, innate and humoral responses have been characterized through acute-phase protein network and auto-antibody signature. Severity and sepsis by SARS-CoV-2 emerged to be correlated with auto-immune profiles of patients and define their clinical progression, which could provide novel perspectives in therapeutics development and biomarkers of COVID-19 patients. Humoral response in COVID-19 patients' profile separates with significant differences patients with or without ARDS. Furthermore, we found that this profile can be correlated with COVID-19 severity and results more common in elderly patients.

Keywords: ARDS; COVID-19; SARS-CoV-2; acute-phase proteins; antigen; auto-antibodies; microarrays; proteomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoantibodies / immunology
  • Autoantigens / immunology*
  • Autoimmunity / immunology*
  • COVID-19 / complications
  • COVID-19 / immunology*
  • Humans
  • Respiratory Distress Syndrome / immunology*
  • Respiratory Distress Syndrome / virology*
  • SARS-CoV-2 / immunology

Substances

  • Autoantibodies
  • Autoantigens