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Preclinical Profile of AB-423, an Inhibitor of Hepatitis B Virus Pregenomic RNA Encapsidation.
Mani, Nagraj; Cole, Andrew G; Phelps, Janet R; Ardzinski, Andrzej; Cobarrubias, Kyle D; Cuconati, Andrea; Dorsey, Bruce D; Evangelista, Ellen; Fan, Kristi; Guo, Fang; Guo, Haitao; Guo, Ju-Tao; Harasym, Troy O; Kadhim, Salam; Kultgen, Steven G; Lee, Amy C H; Li, Alice H L; Long, Quanxin; Majeski, Sara A; Mao, Richeng; McClintock, Kevin D; Reid, Stephen P; Rijnbrand, Rene; Snead, Nicholas M; Micolochick Steuer, Holly M; Stever, Kim; Tang, Sunny; Wang, Xiaohe; Zhao, Qiong; Sofia, Michael J.
Afiliação
  • Mani N; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada nmani@arbutusbio.com.
  • Cole AG; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Phelps JR; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Ardzinski A; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Cobarrubias KD; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Cuconati A; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Dorsey BD; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Evangelista E; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Fan K; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Guo F; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Guo H; Indiana University, Indianapolis, Indiana, USA.
  • Guo JT; Baruch S. Blumberg Institute, Doylestown, Pennsylvania, USA.
  • Harasym TO; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Kadhim S; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Kultgen SG; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Lee ACH; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Li AHL; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Long Q; Indiana University, Indianapolis, Indiana, USA.
  • Majeski SA; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Mao R; Indiana University, Indianapolis, Indiana, USA.
  • McClintock KD; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Reid SP; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Rijnbrand R; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Snead NM; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Micolochick Steuer HM; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Stever K; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Tang S; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Wang X; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
  • Zhao Q; Baruch S. Blumberg Institute, Doylestown, Pennsylvania, USA.
  • Sofia MJ; Arbutus Biopharma Inc., Warminster, Pennsylvania, USA, and Burnaby, British Columbia, Canada.
Article em En | MEDLINE | ID: mdl-29555628
ABSTRACT
AB-423 is a member of the sulfamoylbenzamide (SBA) class of hepatitis B virus (HBV) capsid inhibitors in phase 1 clinical trials. In cell culture models, AB-423 showed potent inhibition of HBV replication (50% effective concentration [EC50] = 0.08 to 0.27 µM; EC90 = 0.33 to 1.32 µM) with no significant cytotoxicity (50% cytotoxic concentration > 10 µM). Addition of 40% human serum resulted in a 5-fold increase in the EC50s. AB-423 inhibited HBV genotypes A through D and nucleos(t)ide-resistant variants in vitro Treatment of HepDES19 cells with AB-423 resulted in capsid particles devoid of encapsidated pregenomic RNA and relaxed circular DNA (rcDNA), indicating that it is a class II capsid inhibitor. In a de novo infection model, AB-423 prevented the conversion of encapsidated rcDNA to covalently closed circular DNA, presumably by interfering with the capsid uncoating process. Molecular docking of AB-423 into crystal structures of heteroaryldihydropyrimidines and an SBA and biochemical studies suggest that AB-423 likely also binds to the dimer-dimer interface of core protein. In vitro dual combination studies with AB-423 and anti-HBV agents, such as nucleos(t)ide analogs, RNA interference agents, or interferon alpha, resulted in additive to synergistic antiviral activity. Pharmacokinetic studies with AB-423 in CD-1 mice showed significant systemic exposures and higher levels of accumulation in the liver. A 7-day twice-daily administration of AB-423 in a hydrodynamic injection mouse model of HBV infection resulted in a dose-dependent reduction in serum HBV DNA levels, and combination with entecavir or ARB-1467 resulted in a trend toward antiviral activity greater than that of either agent alone, consistent with the results of the in vitro combination studies. The overall preclinical profile of AB-423 supports its further evaluation for safety, pharmacokinetics, and antiviral activity in patients with chronic hepatitis B.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Vírus da Hepatite B / Capsídeo / Montagem de Vírus / Hepatite B Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Vírus da Hepatite B / Capsídeo / Montagem de Vírus / Hepatite B Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article