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In vitro antiviral activity and preclinical and clinical resistance profile of miravirsen, a novel anti-hepatitis C virus therapeutic targeting the human factor miR-122.
Ottosen, Søren; Parsley, Todd B; Yang, Lu; Zeh, Karin; van Doorn, Leen-Jan; van der Veer, Eva; Raney, Anneke K; Hodges, Michael R; Patick, Amy K.
Afiliação
  • Ottosen S; Santaris Pharma A/S, Hørsholm, Denmark.
  • Parsley TB; ImQuest BioSciences, Frederick, Maryland, USA.
  • Yang L; ImQuest BioSciences, Frederick, Maryland, USA.
  • Zeh K; Santaris Pharma A/S Corp., San Diego, California, USA.
  • van Doorn LJ; DDL Diagnostic Laboratory, Voorburg, the Netherlands.
  • van der Veer E; DDL Diagnostic Laboratory, Voorburg, the Netherlands.
  • Raney AK; Santaris Pharma A/S Corp., San Diego, California, USA.
  • Hodges MR; Santaris Pharma A/S Corp., San Diego, California, USA.
  • Patick AK; Santaris Pharma A/S Corp., San Diego, California, USA akpatick@gmail.com.
Antimicrob Agents Chemother ; 59(1): 599-608, 2015 Jan.
Article em En | MEDLINE | ID: mdl-25385103
ABSTRACT
Miravirsen is a ß-D-oxy-locked nucleic acid-modified phosphorothioate antisense oligonucleotide targeting the liver-specific microRNA-122 (miR-122). Miravirsen demonstrated antiviral activity against hepatitis C virus (HCV) genotype 1b replicons with a mean 50% effective concentration (EC50) of 0.67 µM. No cytotoxicity was observed up to the highest concentration tested (>320 µM) in different cell culture models, yielding a therapeutic index of ≥ 297. Combination studies of miravirsen with interferon α2b, ribavirin, and nonnucleoside (VX-222) and nucleoside (2'-methylcytidine) inhibitors of NS5B, NS5A (BMS-790052), or NS3 (telaprevir) indicated additive interactions. Miravirsen demonstrated broad antiviral activity when tested against HCV replicons resistant to NS3, NS5A, and NS5B inhibitors with less than 2-fold reductions in susceptibility. In serial passage studies, an A4C nucleotide change was observed in the HCV 5' untranslated region (UTR) from cells passaged in the presence of up to 20 µM (40-fold the miravirsen EC50 concentration) at day 72 of passage but not at earlier time points (up to 39 days of passage). Likewise, a C3U nucleotide change was observed in the HCV 5'UTR from subjects with viral rebound after the completion of therapy in a miravirsen phase 2 clinical trial. An HCV variant constructed to contain the A4C change was fully susceptible to miravirsen. A C3U HCV variant demonstrated overall reductions in susceptibility to miravirsen but was fully susceptible to all other anti-HCV agents tested. In summary, miravirsen has demonstrated broad antiviral activity and a relatively high genetic barrier to resistance. The identification of nucleotide changes associated with miravirsen resistance should help further elucidate the biology of miR-122 interactions with HCV. (The clinical trial study has been registered at ClinicalTrials.gov under registration no. NCT01200420).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antivirais / Oligonucleotídeos / Hepacivirus / Hepatite C Crônica / MicroRNAs Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antivirais / Oligonucleotídeos / Hepacivirus / Hepatite C Crônica / MicroRNAs Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article