Cannabidiol and SARS-CoV-2 Infection

Cannabidiol (CBD) can prevent the inflammatory response of SARS-CoV-2 spike protein in Caco-2-cells. This action is coupled with the inhibition of IL-1beta, IL-6, IL-18, and TNF-alpha, responsible for the inflammatory process during SARS-CoV-2 infection. CBD can act on the different proteins encoded...

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Main Author: Alexandre Vallée
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-03-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.870787/full
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author Alexandre Vallée
author_facet Alexandre Vallée
author_sort Alexandre Vallée
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description Cannabidiol (CBD) can prevent the inflammatory response of SARS-CoV-2 spike protein in Caco-2-cells. This action is coupled with the inhibition of IL-1beta, IL-6, IL-18, and TNF-alpha, responsible for the inflammatory process during SARS-CoV-2 infection. CBD can act on the different proteins encoded by SARS-CoV-2 and as an antiviral agent to prevent the viral infection. Furthermore, recent studies have shown the possible action of CBD as an antagonist of cytokine release syndromes. In the SARS-CoV-2 pathophysiology, the angiotensin-converting enzyme 2 (ACE2) seems to be the key cell receptor for SARS-CoV-2 infection. The WNT/β-catenin pathway and PPARγ interact in an opposite manner in many diseases, including SARS-CoV-2 infection. CBD exerts its activity through the interaction with PPARγ in SARS-CoV-2 infection. Thus, we can hypothesize that CBD may counteract the inflammatory process of SARS-CoV-2 by its interactions with both ACE2 and the interplay between the WNT/β-catenin pathway and PPARγ. Vaccines are the only way to prevent COVID-19, but it appears important to find therapeutic complements to treat patients already affected by SARS-CoV-2 infection. The possible role of CBD should be investigated by clinical trials to show its effectiveness.
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spelling doaj.art-6dcdd0120a68447fac3cd20055007dc02022-12-21T18:13:22ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-03-011310.3389/fimmu.2022.870787870787Cannabidiol and SARS-CoV-2 InfectionAlexandre ValléeCannabidiol (CBD) can prevent the inflammatory response of SARS-CoV-2 spike protein in Caco-2-cells. This action is coupled with the inhibition of IL-1beta, IL-6, IL-18, and TNF-alpha, responsible for the inflammatory process during SARS-CoV-2 infection. CBD can act on the different proteins encoded by SARS-CoV-2 and as an antiviral agent to prevent the viral infection. Furthermore, recent studies have shown the possible action of CBD as an antagonist of cytokine release syndromes. In the SARS-CoV-2 pathophysiology, the angiotensin-converting enzyme 2 (ACE2) seems to be the key cell receptor for SARS-CoV-2 infection. The WNT/β-catenin pathway and PPARγ interact in an opposite manner in many diseases, including SARS-CoV-2 infection. CBD exerts its activity through the interaction with PPARγ in SARS-CoV-2 infection. Thus, we can hypothesize that CBD may counteract the inflammatory process of SARS-CoV-2 by its interactions with both ACE2 and the interplay between the WNT/β-catenin pathway and PPARγ. Vaccines are the only way to prevent COVID-19, but it appears important to find therapeutic complements to treat patients already affected by SARS-CoV-2 infection. The possible role of CBD should be investigated by clinical trials to show its effectiveness.https://www.frontiersin.org/articles/10.3389/fimmu.2022.870787/fullCOVID-19Wnt/β-catenin pathwayPPARγACE2cannabidiolSARS-CoV-2
spellingShingle Alexandre Vallée
Cannabidiol and SARS-CoV-2 Infection
Frontiers in Immunology
COVID-19
Wnt/β-catenin pathway
PPARγ
ACE2
cannabidiol
SARS-CoV-2
title Cannabidiol and SARS-CoV-2 Infection
title_full Cannabidiol and SARS-CoV-2 Infection
title_fullStr Cannabidiol and SARS-CoV-2 Infection
title_full_unstemmed Cannabidiol and SARS-CoV-2 Infection
title_short Cannabidiol and SARS-CoV-2 Infection
title_sort cannabidiol and sars cov 2 infection
topic COVID-19
Wnt/β-catenin pathway
PPARγ
ACE2
cannabidiol
SARS-CoV-2
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.870787/full
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