Complexities of Type I Interferon Biology: Lessons from LCMV

Viruses. 2019 Feb 20;11(2):172. doi: 10.3390/v11020172.

Abstract

Over the past decades, infection of mice with lymphocytic choriomeningitis virus (LCMV) has provided an invaluable insight into our understanding of immune responses to viruses. In particular, this model has clarified the central roles that type I interferons play in initiating and regulating host responses. The use of different strains of LCMV and routes of infection has allowed us to understand how type I interferons are critical in controlling virus replication and fostering effective antiviral immunity, but also how they promote virus persistence and functional exhaustion of the immune response. Accordingly, these discoveries have formed the foundation for the development of novel treatments for acute and chronic viral infections and even extend into the management of malignant tumors. Here we review the fundamental insights into type I interferon biology gained using LCMV as a model and how the diversity of LCMV strains, dose, and route of administration have been used to dissect the molecular mechanisms underpinning acute versus persistent infection. We also identify gaps in the knowledge regarding LCMV regulation of antiviral immunity. Due to its unique properties, LCMV will continue to remain a vital part of the immunologists' toolbox.

Keywords: CD8+ T cells; acute infection; adaptive immune response; chronic infection; innate immune response; lymphocytic choriomeningitis virus; pathogen recognition; type I interferon.

Publication types

  • Review

MeSH terms

  • Acute Disease
  • Adaptive Immunity
  • Animals
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Chronic Disease
  • Clinical Trials as Topic
  • Humans
  • Immunity, Innate
  • Interferon Type I / immunology*
  • Lymphocytic Choriomeningitis / immunology*
  • Lymphocytic choriomeningitis virus / immunology*
  • Mice
  • Mice, Knockout
  • Signal Transduction
  • Virus Replication

Substances

  • Interferon Type I