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Front Immunol ; 13: 732197, 2022.
Article in English | MEDLINE | ID: covidwho-1686479

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.


Subject(s)
Autoantigens/immunology , Autoimmunity/immunology , COVID-19/immunology , Respiratory Distress Syndrome/immunology , Respiratory Distress Syndrome/virology , Autoantibodies/immunology , COVID-19/complications , Humans , SARS-CoV-2/immunology
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