Cannabidiol inhibits SARS-CoV-2 replication through induction of the host ER stress and innate immune responses.
A549 Cells
Animals
Antiviral Agents
/ chemistry
COVID-19
/ virology
Cannabidiol
/ chemistry
Chlorocebus aethiops
Endoplasmic Reticulum Stress
/ drug effects
Endoribonucleases
/ genetics
Epithelial Cells
/ virology
Female
Gene Expression Regulation, Viral
/ drug effects
Host-Pathogen Interactions
/ drug effects
Humans
Immunity, Innate
/ drug effects
Interferons
/ metabolism
Mice
Protein Serine-Threonine Kinases
/ genetics
SARS-CoV-2
/ drug effects
Vero Cells
Virus Internalization
/ drug effects
Virus Replication
/ drug effects
COVID-19 Drug Treatment
Journal
Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440
Informations de publication
Date de publication:
25 Feb 2022
25 Feb 2022
Historique:
pubmed:
21
1
2022
medline:
4
3
2022
entrez:
20
1
2022
Statut:
ppublish
Résumé
The spread of SARS-CoV-2 and ongoing COVID-19 pandemic underscores the need for new treatments. Here we report that cannabidiol (CBD) inhibits infection of SARS-CoV-2 in cells and mice. CBD and its metabolite 7-OH-CBD, but not THC or other congeneric cannabinoids tested, potently block SARS-CoV-2 replication in lung epithelial cells. CBD acts after viral entry, inhibiting viral gene expression and reversing many effects of SARS-CoV-2 on host gene transcription. CBD inhibits SARS-CoV-2 replication in part by up-regulating the host IRE1α RNase endoplasmic reticulum (ER) stress response and interferon signaling pathways. In matched groups of human patients from the National COVID Cohort Collaborative, CBD (100 mg/ml oral solution per medical records) had a significant negative association with positive SARS-CoV-2 tests. This study highlights CBD as a potential preventative agent for early-stage SARS-CoV-2 infection and merits future clinical trials. We caution against use of non-medical formulations including edibles, inhalants or topicals as a preventative or treatment therapy at the present time.
Identifiants
pubmed: 35050692
doi: 10.1126/sciadv.abi6110
pii: 10.1126/sciadv.abi6110
doi:
Substances chimiques
Antiviral Agents
0
Cannabidiol
19GBJ60SN5
Interferons
9008-11-1
ERN1 protein, human
EC 2.7.11.1
Protein Serine-Threonine Kinases
EC 2.7.11.1
Endoribonucleases
EC 3.1.-
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
eabi6110Subventions
Organisme : NIGMS NIH HHS
ID : R35 GM119840
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA184494
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM121735
Pays : United States
Organisme : NCATS NIH HHS
ID : U24 TR002306
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014599
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI137514
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI134980
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI127518
Pays : United States
Commentaires et corrections
Type : UpdateOf