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

Viruses. 2021 Mar 31;13(4):588. doi: 10.3390/v13040588.

Abstract

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.

Keywords: HDV persistence; HDV replication; NTCP; chronic viral hepatitis; hepatitis delta; host restriction factors; human liver chimeric mice; infection; innate immunity; mouse model.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Animals, Genetically Modified*
  • Disease Models, Animal*
  • Hepatitis Delta Virus / physiology*
  • Hepatocytes / virology*
  • Host Microbial Interactions
  • Humans
  • Mice
  • Organic Anion Transporters, Sodium-Dependent / genetics*
  • Symporters / genetics*
  • Virus Internalization*

Substances

  • Organic Anion Transporters, Sodium-Dependent
  • Symporters
  • sodium-bile acid cotransporter