CD8 T cells specific for lymphocytic choriomeningitis virus require type I IFN receptor for clonal expansion

J Immunol. 2006 Apr 15;176(8):4525-9. doi: 10.4049/jimmunol.176.8.4525.

Abstract

The role of type I IFN signaling in CD8 T cells was analyzed in an adoptive transfer model using P14 TCR transgenic CD8 T cells specific for lymphocytic choriomeningitis virus (LCMV) but deficient in type I IFNR. In the present study, we demonstrate severe impairment in the capacity of P14 T cells lacking type I IFNR to expand in normal type I IFNR wild-type C57BL/6 hosts after LCMV infection. In contrast, following infection of recipient mice with recombinant vaccinia virus expressing LCMV glycoprotein, P14 T cell expansion was considerably less dependent on type I IFNR expression. Lack of type I IFNR expression by P14 T cells did not affect cell division after LCMV infection but interfered with clonal expansion. Thus, direct type I IFN signaling is essential for CD8 T cell survival in certain viral infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • Antigens, Viral / immunology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / pathology
  • Cell Proliferation
  • Glycoproteins / immunology
  • Interferon gamma Receptor
  • Lymphocyte Activation
  • Lymphocytic Choriomeningitis / immunology
  • Lymphocytic Choriomeningitis / pathology
  • Lymphocytic choriomeningitis virus / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Peptide Fragments / immunology
  • Receptors, Interferon / immunology*
  • Viral Proteins / immunology

Substances

  • Antigens, Viral
  • Glycoproteins
  • Peptide Fragments
  • Receptors, Interferon
  • Viral Proteins
  • glycoprotein peptide 33-41, Lymphocytic choriomeningitis virus