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Arbidol: a broad-spectrum antiviral that inhibits acute and chronic HCV infection
Boriskin, Yury S ; Pécheur, Eve-Isabelle ; Polyak, Stephen J
Virology journal, 2006-07, Vol.3 (1), p.56-56, Article 56
[Peer Reviewed Journal]
England: BioMed Central Ltd
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Title:
Arbidol: a broad-spectrum antiviral that inhibits acute and chronic HCV infection
Author:
Boriskin, Yury S
;
Pécheur, Eve-Isabelle
;
Polyak, Stephen J
Subjects:
Acute Disease
;
Antiviral
Agents
- pharmacology
;
Biochemistry, Molecular Biology
;
Carcinoma, Hepatocellular - pathology
;
Carcinoma, Hepatocellular - virology
;
Cell Line, Tumor
;
Cell Survival - drug effects
;
Hepacivirus - physiology
;
Hepatitis C - drug therapy
;
Hepatitis C - genetics
;
Hepatitis C - metabolism
;
Hepatitis C - prevention & control
;
Hepatitis C - virology
;
Hepatitis C virus
;
Hepatitis C, Chronic - drug therapy
;
Hepatitis C, Chronic - genetics
;
Hepatitis C, Chronic - metabolism
;
Hepatitis C, Chronic - virology
;
Humans
;
Indoles - pharmacology
;
Interferon-beta - genetics
;
Interferon-beta - metabolism
;
Life Sciences
;
Membrane Fusion - drug effects
;
Microbial Viability - drug effects
;
Receptors, Retinoic Acid - metabolism
;
RNA, Viral - biosynthesis
;
RNA, Viral - genetics
;
Signal Transduction - drug effects
;
Virus Replication - drug effects
Is Part Of:
Virology journal, 2006-07, Vol.3 (1), p.56-56, Article 56
Notes:
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Description:
Arbidol (ARB) is an antiviral compound that was originally proven effective for treatment of influenza and several other respiratory viral infections. The broad spectrum of ARB anti-viral activity led us to evaluate its effect on hepatitis C virus (HCV) infection and replication in cell culture. Long-term ARB treatment of Huh7 cells chronically replicating a genomic length genotype 1b replicon resulted in sustained reduction of viral RNA and protein expression, and eventually cured HCV infected cells. Pre-treatment of human hepatoma Huh7.5.1 cells with 15 microM ARB for 24 to 48 hours inhibited acute infection with JFH-1 virus by up to 1000-fold. The inhibitory effect of ARB on HCV was not due to generalized cytotoxicity, nor to augmentation of IFN antiviral signaling pathways, but involved impaired virus-mediated membrane fusion. ARB's affinity for membranes may inhibit several aspects of the HCV lifecycle that are membrane-dependent.
Publisher:
England: BioMed Central Ltd
Language:
English
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