It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
A major unmet clinical need is a therapeutic capable of removing hepatitis B virus (HBV) genome from the liver of infected individuals to reduce their risk of developing liver cancer. A strategy to deliver such a therapy could utilize the ability to target and promote apoptosis of infected hepatocytes. Presently there is no clinically relevant strategy that has been shown to effectively remove persistent episomal covalently closed circular HBV DNA (cccDNA) from the nucleus of hepatocytes. We used linearized single genome length HBV DNA of various genotypes to establish a cccDNA-like reservoir in immunocompetent mice and showed that clinical-stage orally administered drugs that antagonize the function of cellular inhibitor of apoptosis proteins can eliminate HBV replication and episomal HBV genome in the liver. Primary human liver organoid models were used to confirm the clinical relevance of these results. This study underscores a clinically tenable strategy for the potential elimination of chronic HBV reservoirs in patients.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details





1 The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia (GRID:grid.1042.7); The University of Melbourne, Department of Medical Biology, Parkville, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X)
2 The Royal Melbourne Hospital at The Peter Doherty Institute for Infection and Immunity, Victorian Infectious Diseases Reference Laboratory, Melbourne, Australia (GRID:grid.416153.4) (ISNI:0000 0004 0624 1200)
3 Erasmus University Medical Center, Rotterdam, The Netherlands (GRID:grid.5645.2) (ISNI:000000040459992X)
4 The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia (GRID:grid.1042.7)
5 The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia (GRID:grid.1042.7); The University of Melbourne, Department of Medical Biology, Parkville, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X); Oregon Health and Science University, Vaccine and Gene Therapy Institute, Beaverton, USA (GRID:grid.5288.7) (ISNI:0000 0000 9758 5690)
6 Yonsei University, Department of Internal Medicine, Seoul, South Korea (GRID:grid.15444.30) (ISNI:0000 0004 0470 5454)
7 The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Department of Microbiology and Immunology, Melbourne, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X)
8 The Royal Melbourne Hospital at The Peter Doherty Institute for Infection and Immunity, Victorian Infectious Diseases Reference Laboratory, Melbourne, Australia (GRID:grid.416153.4) (ISNI:0000 0004 0624 1200); The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Department of Infectious Diseases, Melbourne, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X)
9 The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Department of Infectious Diseases, Melbourne, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X)
10 Debiopharm International S.A., Lausanne, Switzerland (GRID:grid.476201.6) (ISNI:0000 0004 0627 5347)
11 The Royal Melbourne Hospital at The Peter Doherty Institute for Infection and Immunity, Victorian Infectious Diseases Reference Laboratory, Melbourne, Australia (GRID:grid.416153.4) (ISNI:0000 0004 0624 1200); The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Department of Infectious Diseases, Melbourne, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X); Curtin University, Curtin Medical School, Perth, Australia (GRID:grid.1032.0) (ISNI:0000 0004 0375 4078)
12 The Royal Melbourne Hospital at The Peter Doherty Institute for Infection and Immunity, Victorian Infectious Diseases Reference Laboratory, Melbourne, Australia (GRID:grid.416153.4) (ISNI:0000 0004 0624 1200); The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Department of Microbiology and Immunology, Melbourne, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X)
13 The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia (GRID:grid.1042.7); The University of Melbourne, Department of Medical Biology, Parkville, Australia (GRID:grid.1008.9) (ISNI:0000 0001 2179 088X); Technical University of Munich/Helmholtz Zentrum München, Institute of Virology, Munich, Germany (GRID:grid.6936.a) (ISNI:0000000123222966)