NLRC4 inflammasomes in dendritic cells regulate noncognate effector function by memory CD8⁺ T cells

Nat Immunol. 2012 Jan 8;13(2):162-9. doi: 10.1038/ni.2195.

Abstract

Memory T cells exert antigen-independent effector functions, but how these responses are regulated is unclear. We discovered an in vivo link between flagellin-induced NLRC4 inflammasome activation in splenic dendritic cells (DCs) and host protective interferon-γ (IFN-γ) secretion by noncognate memory CD8(+) T cells, which could be activated by Salmonella enterica serovar Typhimurium, Yersinia pseudotuberculosis and Pseudomonas aeruginosa. We show that CD8α(+) DCs were particularly efficient at sensing bacterial flagellin through NLRC4 inflammasomes. Although this activation released interleukin 18 (IL-18) and IL-1β, only IL-18 was required for IFN-γ production by memory CD8(+) T cells. Conversely, only the release of IL-1β, but not IL-18, depended on priming signals mediated by Toll-like receptors. These findings provide a comprehensive mechanistic framework for the regulation of noncognate memory T cell responses during bacterial immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • Calcium-Binding Proteins / immunology*
  • Dendritic Cells / immunology*
  • Flagellin / immunology
  • Immunologic Memory*
  • Inflammasomes / immunology*
  • Interferon-gamma / immunology*
  • Interleukin-18 / immunology
  • Interleukin-1beta / immunology
  • Interleukin-1beta / metabolism
  • Mice
  • Pseudomonas Infections / immunology
  • Pseudomonas aeruginosa / immunology
  • Salmonella Infections, Animal / immunology
  • Salmonella typhimurium / immunology
  • Signal Transduction / immunology
  • Spleen / immunology
  • Toll-Like Receptors / immunology
  • Yersinia pseudotuberculosis Infections / immunology

Substances

  • Apoptosis Regulatory Proteins
  • Calcium-Binding Proteins
  • Inflammasomes
  • Interleukin-18
  • Interleukin-1beta
  • Ipaf protein, mouse
  • Toll-Like Receptors
  • Flagellin
  • Interferon-gamma