IL-21R on T cells is critical for sustained functionality and control of chronic viral infection

Science. 2009 Jun 19;324(5934):1576-80. doi: 10.1126/science.1172815. Epub 2009 May 28.

Abstract

Chronic viral infection is often associated with the dysfunction of virus-specific T cells. Our studies using Il21r-deficient (Il21r-/-) mice now suggest that interleukin-21 (IL-21) is critical for the long-term maintenance and functionality of CD8+ T cells and the control of chronic lymphocytic choriomeningitis virus infection in mice. Cell-autonomous IL-21 receptor (IL-21R)-dependent signaling by CD8+ T cells was required for sustained cell proliferation and cytokine production during chronic infection. Il21r-/- mice showed normal CD8+ T cell expansion, effector function, memory homeostasis, and recall responses during acute and after resolved infection with several other nonpersistent viruses. These data suggest that IL-21R signaling is required for the maintenance of polyfunctional T cells during chronic viral infections and have implications for understanding the immune response to other persisting antigens, such as tumors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • Chronic Disease
  • Humans
  • Immunologic Memory
  • Interferon-gamma / biosynthesis
  • Lymphocytic Choriomeningitis / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Peptide Fragments / biosynthesis
  • Receptors, Interleukin-21 / immunology*
  • Signal Transduction

Substances

  • Peptide Fragments
  • Receptors, Interleukin-21
  • interferon gamma (1-39)
  • Interferon-gamma