Viral infections in mice with reconstituted human immune system components

Immunol Lett. 2014 Sep;161(1):118-24. doi: 10.1016/j.imlet.2014.05.012. Epub 2014 Jun 2.

Abstract

Pathogenic viruses are often difficult to study due to their exclusive tropism for humans. The development of mice with human immune system components opens the possibility to study those human pathogens with a tropism for the human hematopoietic lineage in vivo. These include HCMV, EBV, KSHV, HIV, HTLV-1, dengue virus and JC virus. Furthermore, some human pathogens, like HSV-2, adenovirus, HCV, HBV and influenza A virus, with an additional tropism for somatic mouse tissues or for additional transplanted human tissues, mainly liver, have been explored in these models. The cellular tropism of these viruses, their associated diseases and primarily cell-mediated immune responses to these viral infections will be discussed in this review. Already some exciting information has been gained from these novel chimeric in vivo models and future avenues to gain more insights into the pathology, but also potential therapies, will be outlined. Although the respective in vivo models of human immune responses can still be significantly improved, they already provide preclinical systems for in vivo studies of important viral pathogens of humans.

Keywords: Dengue virus; EBV; HIV; NK cells; T cells.

Publication types

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

MeSH terms

  • Animals
  • Disease Models, Animal
  • Host-Pathogen Interactions
  • Humans
  • Immune System / physiology*
  • Immunologic Surveillance / genetics
  • Immunologic Surveillance / immunology
  • Mice
  • Virus Diseases / immunology*
  • Virus Diseases / virology*