Mice with Chimeric Human Livers and Their Applications

Methods Mol Biol. 2019:1911:459-479. doi: 10.1007/978-1-4939-8976-8_32.

Abstract

The complete life cycle of the hepatitis C virus (HCV) can be recapitulated in vivo using immunodeficient mice that have had their livers extensively repopulated with human hepatocytes. These human liver chimeric mouse models have enabled the study of many aspects of the HCV life cycle, including antiviral interventions that have helped to shape the curative landscape that is available today. The first human liver chimeric mouse model capable of supporting the HCV life cycle was generated in SCID-uPA mice. Although other human liver chimeric mouse models have since been developed, the SCID-uPA mouse model remains one of the most robust in vivo systems available for HCV studies. This chapter reviews development, validation and application of the SCID-uPA mouse model, and discusses their potential application for studying other liver-centric diseases and pathogens and for the design and testing of vaccine candidates for the eradication of HCV.

Keywords: Animal models; Antiviral therapy; Pathology; Viral hepatitis.

Publication types

  • Review

MeSH terms

  • Animals
  • Disease Models, Animal*
  • Hepacivirus / physiology*
  • Hepatitis C / immunology*
  • Hepatitis C / virology
  • Hepatocytes / immunology
  • Hepatocytes / virology
  • Humans
  • Liver / immunology*
  • Liver / virology
  • Liver Transplantation
  • Mice
  • Mice, SCID
  • Transplantation Chimera
  • Urokinase-Type Plasminogen Activator / genetics*
  • Urokinase-Type Plasminogen Activator / immunology

Substances

  • Urokinase-Type Plasminogen Activator