Insights into the modulation of the interferon response and NAD in the context of COVID-19.

Nada J Habeichi, Cynthia Tannous, Andriy Yabluchanskiy, Raffaele Altara, Mathias Mericskay, George W Booz, Fouad A Zouein

Journal: International reviews of immunology 2022;41(4):464-474

PMID: 34378474

Abstract

The COVID-19 pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in dramatic worldwide mortality. Along with developing vaccines, the medical profession is exploring new strategies to curb this pandemic. A better understanding of the molecular consequences of SARS-CoV-2 cellular infection could lead to more effective and safer treatments. This review discusses the potential underlying impact of SARS-CoV-2 in modulating interferon (IFN) secretion and in causing mitochondrial NAD depletion that could be directly linked to COVID-19's deadly manifestations. What is known or surmised about an imbalanced innate immune response and mitochondrial dysfunction post-SARS-CoV-2 infection, and the potential benefits of well-timed IFN treatments and NAD boosting therapies in the context of the COVID-19 pandemic are discussed.

Address: Department of Pharmacology and Toxicology, American University of Beirut Faculty of Medicine, Beirut, Lebanon.; Department of Signaling and Cardiovascular Pathophysiology, Université Paris-Saclay, Inserm, UMR-S 1180, Châtenay-Malabry, France.; Center for Geroscience and Healthy Brain Aging, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.; Institute for Experimental Medical Research, Oslo University Hospital and University of Oslo, Oslo, Norway.; KG Jebsen Center for Cardiac Research, Oslo, Norway.; Department of Pathology, School of Medicine, University of Mississippi Medical Center, Jackson, MS, USA.; Department of Pharmacology and Toxicology, School of Medicine, University of Mississippi Medical Center, Jackson, MS, USA.

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