High IFN-gamma production of individual CD8 T lymphocytes is controlled by CD152 (CTLA-4)

J Immunol. 2007 Feb 15;178(4):2132-40. doi: 10.4049/jimmunol.178.4.2132.

Abstract

CD8 T cell expansion and cytokine production is needed to generate an effective defense against viral invasion of the host. These features of CD8 T lymphocytes are regulated, especially during primary responses, by positive and negative costimulation. We show in this study that surface expression of CD152 is highly up-regulated on activated CD8 T lymphocytes during primary immune responses, suggesting a prominent regulatory role. Indeed, production of the proinflammatory cytokine IFN-gamma, but not TNF-alpha, by CD8 T cells was inhibited by CD152 engagement. The inhibition was regulated independent of proliferation and IL-2 production, but dependent on the quality of the TCR signaling. We show that signals induced by CD152 on activated CD8 T lymphocytes reduce the frequency of IFN-gamma(high)-expressing cells. Our data also show that in activated CD8 T cells, the CD152-mediated inhibition of cytokine production is more pronounced than inhibition of their proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / immunology*
  • Antigens, CD / metabolism
  • Antigens, Differentiation / genetics
  • Antigens, Differentiation / immunology*
  • Antigens, Differentiation / metabolism
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • CTLA-4 Antigen
  • Cell Proliferation
  • Inflammation / immunology
  • Inflammation / metabolism
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / immunology*
  • Interleukin-2 / biosynthesis
  • Interleukin-2 / immunology
  • Lymphocyte Activation*
  • Mice
  • Mice, Knockout
  • Signal Transduction / immunology*
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / immunology
  • Up-Regulation / immunology*

Substances

  • Antigens, CD
  • Antigens, Differentiation
  • CTLA-4 Antigen
  • Ctla4 protein, mouse
  • Interleukin-2
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma