Obesity and Leptin Resistance in the Regulation of the Type I Interferon Early Response and the Increased Risk for Severe COVID-19.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
26 Mar 2022
Historique:
received: 21 02 2022
revised: 23 03 2022
accepted: 23 03 2022
entrez: 12 4 2022
pubmed: 13 4 2022
medline: 14 4 2022
Statut: epublish

Résumé

Obesity, and obesity-associated conditions such as hypertension, chronic kidney disease, type 2 diabetes, and cardiovascular disease, are important risk factors for severe Coronavirus disease-2019 (COVID-19). The common denominator is metaflammation, a portmanteau of metabolism and inflammation, which is characterized by chronically elevated levels of leptin and pro-inflammatory cytokines. These induce the "Suppressor Of Cytokine Signaling 1 and 3" (SOCS1/3), which deactivates the leptin receptor and also other SOCS1/3 sensitive cytokine receptors in immune cells, impairing the type I and III interferon early responses. By also upregulating SOCS1/3, Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV)-2 adds a significant boost to this. The ensuing consequence is a delayed but over-reactive immune response, characterized by high-grade inflammation (e.g., cytokine storm), endothelial damage, and hypercoagulation, thus leading to severe COVID-19. Superimposing an acute disturbance, such as a SARS-CoV-2 infection, on metaflammation severely tests resilience. In the long run, metaflammation causes the "typical western" conditions associated with metabolic syndrome. Severe COVID-19 and other serious infectious diseases can be added to the list of its short-term consequences. Therefore, preventive measures should include not only vaccination and the well-established actions intended to avoid infection, but also dietary and lifestyle interventions aimed at improving body composition and preventing or reversing metaflammation.

Identifiants

pubmed: 35406000
pii: nu14071388
doi: 10.3390/nu14071388
pmc: PMC9002648
pii:
doi:

Substances chimiques

Interferon Type I 0
Leptin 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Frits A J Muskiet (FAJ)

Department of Laboratory Medicine, University Medical Center Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands.

Pedro Carrera-Bastos (P)

Center for Primary Health Care Research, Lund University, 205 02 Malmö, Sweden.
Faculty of Biomedical and Health Sciences, Universidad Europea de Madrid, 28670 Madrid, Spain.
Centro de Estudios Avanzados en Nutrición (CEAN), 11007 Cádiz, Spain.

Leo Pruimboom (L)

Natura Foundation, 3281 NC Numansdorp, The Netherlands.

Alejandro Lucia (A)

Faculty of Sport Sciences, Universidad Europea de Madrid, 28670 Madrid, Spain.
Physical Activity and Health Research Group ('PaHerg'), Research Institute of the Hospital 12 de Octubre ('imas12'), 28041 Madrid, Spain.
Biomedical Research Networking Center on Frailty and Healthy Aging (CIBERFES), 28029 Madrid, Spain.

David Furman (D)

Stanford 1000 Immunomes Project, Stanford University School of Medicine, Stanford, CA 94305, USA.
Buck Artificial Intelligence Platform, The Buck Institute for Research on Aging, Novato, CA 94945, USA.
Edifice Health Inc., San Mateo, CA 94401, USA.
Austral Institute for Applied Artificial Intelligence, Institute for Research in Translational Medicine (IIMT), Universidad Austral, National Scientific and Technical Research Council (CONICET), Buenos Aires 2290, Argentina.

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