Herpesvirus-Associated Lymphadenitis Distorts Fibroblastic Reticular Cell Microarchitecture and Attenuates CD8 T Cell Responses to Neurotropic Infection in Mice Lacking the STING-IFNα/β Defense Pathways

J Immunol. 2016 Sep 15;197(6):2338-52. doi: 10.4049/jimmunol.1600574. Epub 2016 Aug 10.

Abstract

Type I IFN (IFN-α/β)-driven immune responses to acute viral infection are critical to counter replication and prevent dissemination. However, the mechanisms underlying host resistance to HSV type 1 (HSV-1) are incompletely understood. In this study, we show that mice with deficiencies in IFN-α/β signaling or stimulator of IFN genes (STING) exhibit exacerbated neurovirulence and atypical lymphotropic dissemination of HSV-1 following ocular infection. Synergy between IFN-α/β signaling and efficacy of early adaptive immune responses to HSV-1 were dissected using bone marrow chimeras and adoptive cell transfer approaches to profile clonal expansion, effector function, and recruitment of HSV-specific CD8(+) T cells. Lymphotropic viral dissemination was commensurate with abrogated CD8(+) T cell responses and pathological alterations of fibroblastic reticular cell networks in the draining lymph nodes. Our results show that resistance to HSV-1 in the trigeminal ganglia during acute infection is conferred in part by STING and IFN-α/β signaling in both bone marrow-derived and -resident cells, which coalesce to support a robust HSV-1-specific CD8(+) T cell response.

MeSH terms

  • Adaptive Immunity
  • Adoptive Transfer
  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / pathology
  • Eye / virology
  • Herpes Simplex / immunology
  • Herpes Simplex / virology*
  • Herpesvirus 1, Human / immunology*
  • Herpesvirus 1, Human / pathogenicity
  • Herpesvirus 1, Human / physiology
  • Interferon beta-1a / genetics
  • Interferon beta-1a / immunology
  • Interferon beta-1a / metabolism*
  • Interferon-alpha / genetics
  • Interferon-alpha / immunology
  • Interferon-alpha / metabolism*
  • Lymphadenitis / immunology*
  • Lymphadenitis / physiopathology
  • Lymphadenitis / virology*
  • Membrane Proteins / deficiency
  • Membrane Proteins / metabolism*
  • Mice
  • Signal Transduction
  • Trigeminal Ganglion / immunology
  • Trigeminal Ganglion / physiopathology
  • Trigeminal Ganglion / virology
  • Virus Replication

Substances

  • Interferon-alpha
  • Membrane Proteins
  • Sting1 protein, mouse
  • Interferon beta-1a