No evidence for drug resistance by iminosugar-based HCV assembly inhibitors in tissue culture

At present, neither a selective antiviral therapy nor a vaccine is available for HCV, and the current treatment is only effective in a fraction of patients. Given the recent demonstration that antiviral compounds targeting the NS5B polymerase and the NS3/4A protease lead to rapid selection for resis...

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Main Authors: Steinmann, E, Friesland, M, Ciesek, S, Zitzmann, N, Pietschmann, T
Format: Journal article
Published: Elsevier 2010
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author Steinmann, E
Friesland, M
Ciesek, S
Zitzmann, N
Pietschmann, T
author_facet Steinmann, E
Friesland, M
Ciesek, S
Zitzmann, N
Pietschmann, T
author_sort Steinmann, E
collection OXFORD
description At present, neither a selective antiviral therapy nor a vaccine is available for HCV, and the current treatment is only effective in a fraction of patients. Given the recent demonstration that antiviral compounds targeting the NS5B polymerase and the NS3/4A protease lead to rapid selection for resistance, iminosugar derivatives as HCV assembly inhibitors were characterized for drug resistance. It has been previously shown that deoxynojirimycin (DNJ)-containing iminosugars are potent HCV antivirals inhibiting ER alpha-glucosidases I and II. Long alkyl chain derivatives such asNN-DGJ inhibit the HCV p7 ion channel activityin vitro. The aim of this study was to characterize the drug resistance profile of an inhibitor targeting cellular enzymes (NB-DNJ) and of the p7 inhibitor NN-DGJ in comparison to the NS5B polymerase inhibitor 2’C-methyladenosine (2CMA).
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spelling oxford-uuid:ca51c17f-8eb1-473e-bd27-7bf46cd1b6c72022-03-27T07:06:31ZNo evidence for drug resistance by iminosugar-based HCV assembly inhibitors in tissue cultureJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:ca51c17f-8eb1-473e-bd27-7bf46cd1b6c7Symplectic Elements at OxfordElsevier2010Steinmann, EFriesland, MCiesek, SZitzmann, NPietschmann, TAt present, neither a selective antiviral therapy nor a vaccine is available for HCV, and the current treatment is only effective in a fraction of patients. Given the recent demonstration that antiviral compounds targeting the NS5B polymerase and the NS3/4A protease lead to rapid selection for resistance, iminosugar derivatives as HCV assembly inhibitors were characterized for drug resistance. It has been previously shown that deoxynojirimycin (DNJ)-containing iminosugars are potent HCV antivirals inhibiting ER alpha-glucosidases I and II. Long alkyl chain derivatives such asNN-DGJ inhibit the HCV p7 ion channel activityin vitro. The aim of this study was to characterize the drug resistance profile of an inhibitor targeting cellular enzymes (NB-DNJ) and of the p7 inhibitor NN-DGJ in comparison to the NS5B polymerase inhibitor 2’C-methyladenosine (2CMA).
spellingShingle Steinmann, E
Friesland, M
Ciesek, S
Zitzmann, N
Pietschmann, T
No evidence for drug resistance by iminosugar-based HCV assembly inhibitors in tissue culture
title No evidence for drug resistance by iminosugar-based HCV assembly inhibitors in tissue culture
title_full No evidence for drug resistance by iminosugar-based HCV assembly inhibitors in tissue culture
title_fullStr No evidence for drug resistance by iminosugar-based HCV assembly inhibitors in tissue culture
title_full_unstemmed No evidence for drug resistance by iminosugar-based HCV assembly inhibitors in tissue culture
title_short No evidence for drug resistance by iminosugar-based HCV assembly inhibitors in tissue culture
title_sort no evidence for drug resistance by iminosugar based hcv assembly inhibitors in tissue culture
work_keys_str_mv AT steinmanne noevidencefordrugresistancebyiminosugarbasedhcvassemblyinhibitorsintissueculture
AT frieslandm noevidencefordrugresistancebyiminosugarbasedhcvassemblyinhibitorsintissueculture
AT cieseks noevidencefordrugresistancebyiminosugarbasedhcvassemblyinhibitorsintissueculture
AT zitzmannn noevidencefordrugresistancebyiminosugarbasedhcvassemblyinhibitorsintissueculture
AT pietschmannt noevidencefordrugresistancebyiminosugarbasedhcvassemblyinhibitorsintissueculture