MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling

J Immunol Res. 2019 Sep 9:2019:5370706. doi: 10.1155/2019/5370706. eCollection 2019.

Abstract

MHC class I molecules are key in the presentation of antigen and initiation of adaptive CD8+ T cell responses. In addition to its classical activity, MHC I may possess nonclassical functions. We have previously identified a regulatory role of MHC I in TLR signaling and antibacterial immunity. However, its role in innate antiviral immunity remains unknown. In this study, we found a reduced viral load in MHC I-deficient macrophages that was independent of type I IFN production. Mechanically, MHC I mediated viral suppression by inhibiting the type I IFN signaling pathway, which depends on SHP2. Cross-linking MHC I at the membrane increased SHP2 activation and further suppressed STAT1 phosphorylation. Therefore, our data revealed an inhibitory role of MHC I in type I IFN response to viral infection and expanded our understanding of MHC I and antigen presentation.

MeSH terms

  • Animals
  • Cell Line
  • Disease Models, Animal
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class I / metabolism*
  • Humans
  • Interferon Type I / metabolism
  • Mice
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11 / metabolism
  • Signal Transduction*
  • Virus Diseases / immunology
  • Virus Diseases / metabolism*
  • Virus Diseases / virology*
  • Virus Replication

Substances

  • Histocompatibility Antigens Class I
  • Interferon Type I
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11