In Vivo Models of HDV Infection: Is Humanizing NTCP Enough?

The discovery of sodium taurocholate co-transporting polypeptide (NTCP) as a hepatitis B (HBV) and delta virus (HDV) entry receptor has encouraged the development of new animal models of infection. This review provides an overview of the different in vivo models that are currently available to study...

Full description

Bibliographic Details
Main Authors: Katja Giersch, Maura Dandri
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/4/588
_version_ 1827696329387671552
author Katja Giersch
Maura Dandri
author_facet Katja Giersch
Maura Dandri
author_sort Katja Giersch
collection DOAJ
description The discovery of sodium taurocholate co-transporting polypeptide (NTCP) as a hepatitis B (HBV) and delta virus (HDV) entry receptor has encouraged the development of new animal models of infection. This review provides an overview of the different in vivo models that are currently available to study HDV either in the absence or presence of HBV. By presenting new advances and remaining drawbacks, we will discuss human host factors which, in addition to NTCP, need to be investigated or identified to enable a persistent HDV infection in murine hepatocytes. Detailed knowledge on species-specific factors involved in HDV persistence also shall contribute to the development of therapeutic strategies.
first_indexed 2024-03-10T12:45:09Z
format Article
id doaj.art-10589d8f17ea4f768497204a2c09f49c
institution Directory Open Access Journal
issn 1999-4915
language English
last_indexed 2024-03-10T12:45:09Z
publishDate 2021-03-01
publisher MDPI AG
record_format Article
series Viruses
spelling doaj.art-10589d8f17ea4f768497204a2c09f49c2023-11-21T13:31:30ZengMDPI AGViruses1999-49152021-03-0113458810.3390/v13040588In Vivo Models of HDV Infection: Is Humanizing NTCP Enough?Katja Giersch0Maura Dandri1Department of Internal Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, GermanyDepartment of Internal Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, GermanyThe discovery of sodium taurocholate co-transporting polypeptide (NTCP) as a hepatitis B (HBV) and delta virus (HDV) entry receptor has encouraged the development of new animal models of infection. This review provides an overview of the different in vivo models that are currently available to study HDV either in the absence or presence of HBV. By presenting new advances and remaining drawbacks, we will discuss human host factors which, in addition to NTCP, need to be investigated or identified to enable a persistent HDV infection in murine hepatocytes. Detailed knowledge on species-specific factors involved in HDV persistence also shall contribute to the development of therapeutic strategies.https://www.mdpi.com/1999-4915/13/4/588mouse modelinfectionhepatitis deltaNTCPhuman liver chimeric miceHDV persistence
spellingShingle Katja Giersch
Maura Dandri
In Vivo Models of HDV Infection: Is Humanizing NTCP Enough?
Viruses
mouse model
infection
hepatitis delta
NTCP
human liver chimeric mice
HDV persistence
title In Vivo Models of HDV Infection: Is Humanizing NTCP Enough?
title_full In Vivo Models of HDV Infection: Is Humanizing NTCP Enough?
title_fullStr In Vivo Models of HDV Infection: Is Humanizing NTCP Enough?
title_full_unstemmed In Vivo Models of HDV Infection: Is Humanizing NTCP Enough?
title_short In Vivo Models of HDV Infection: Is Humanizing NTCP Enough?
title_sort in vivo models of hdv infection is humanizing ntcp enough
topic mouse model
infection
hepatitis delta
NTCP
human liver chimeric mice
HDV persistence
url https://www.mdpi.com/1999-4915/13/4/588
work_keys_str_mv AT katjagiersch invivomodelsofhdvinfectionishumanizingntcpenough
AT mauradandri invivomodelsofhdvinfectionishumanizingntcpenough