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Coronavirus disease 2019 (COVID-19) update: From metabolic reprogramming to immunometabolism

Authors :
Mohammad Rudiansyah
Saade Abdalkareem Jasim
Zeinab Gol Mohammad pour
Sara Sohrabi Athar
Ali Salimi Jeda
Rumi Iqbal doewes
Abduladheem Turki Jalil
D. O. Bokov
Yasser Fakri Mustafa
Mina Noroozbeygi
Sajad Karampoor
Rasoul Mirzaei
Source :
Journal of medical virology. 94(10)
Publication Year :
2022

Abstract

The field of immunometabolism investigates and describes the effects of metabolic rewiring in immune cells throughout activation and the fates of these cells. Recently, it has been appreciated that immunometabolism plays an essential role in the progression of viral infections, cancer, and autoimmune diseases. Regarding COVID-19, the aberrant immune response underlying the progression of diseases establishes two major respiratory pathologies, including acute respiratory distress syndrome (ARDS) or pneumonia-induced acute lung injury (ALI). Both innate and adaptive immunity (T cell-based) were impaired in the course of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Current findings have deciphered that macrophages (innate immune cells) are involved in the inflammatory response seen in COVID-19. It has been demonstrated that immune system cells can change metabolic reprogramming in some conditions, including autoimmune diseases, cancer, and infectious disease, including COVID-19. The growing findings on metabolic reprogramming in COVID-19 allow an exploration of metabolites with immunomodulatory properties as future therapies to combat this hyperinflammatory response. The elucidation of the exact role and mechanism underlying this metabolic reprograming in immune cells could help apply more precise approaches to initial diagnosis, prognosis, and in-hospital therapy. This report discusses the latest findings from COVID-19 on host metabolic reprogramming and immunometabolic responses.

Details

ISSN :
10969071
Volume :
94
Issue :
10
Database :
OpenAIRE
Journal :
Journal of medical virology
Accession number :
edsair.doi.dedup.....cc7a2a9fcb4970b1321a83e1e3d9ad3a