Production of interleukin-27 by human neutrophils regulates their function during bacterial infection

Eur J Immunol. 2012 Dec;42(12):3280-90. doi: 10.1002/eji.201242526. Epub 2012 Oct 25.

Abstract

Septicemia is the most severe form of melioidosis caused by the Gram-negative bacterium, Burkholderia pseudomallei. Here, we show that levels of IL-27p28 transcript and protein were both significantly elevated in patients with sepsis, particularly melioidosis and in patients with unfavorable disease outcome. Moreover, human monocytes/macrophages and neutrophils were the major source of IL-27 during infection. The addition of exogenous IL-27 in vitro resulted in significantly increased bacterial survival, reduced B. pseudomallei-induced oxidative burst, and enhanced IL-1β and TNF-α production by purified neutrophils from healthy subjects. Finally, blockade of endogenous IL-27 in neutrophils using soluble IL-27 receptor antagonist prior to infection led to significantly reduced survival of bacteria and decreased IL-1β, but not TNF-α production. These results indicate a potential role for IL-27 in the suppression of anti-bacterial defense mechanisms that might contribute to disease severity in sepsis. The targeting of this cytokine may be beneficial in the management of human sepsis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Burkholderia pseudomallei / immunology*
  • Female
  • Gene Expression Regulation / immunology*
  • Humans
  • Interleukin-1beta / biosynthesis
  • Interleukin-1beta / immunology
  • Interleukins / biosynthesis
  • Interleukins / immunology*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Male
  • Melioidosis / drug therapy
  • Melioidosis / immunology*
  • Melioidosis / metabolism
  • Middle Aged
  • Monocytes / immunology
  • Monocytes / metabolism
  • Neutrophils / immunology*
  • Neutrophils / metabolism
  • Respiratory Burst / immunology*
  • Sepsis / drug therapy
  • Sepsis / immunology
  • Sepsis / metabolism
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • IL1B protein, human
  • Interleukin-1beta
  • Interleukins
  • MYDGF protein, human
  • Tumor Necrosis Factor-alpha