Anti-inflammatory cytokine response and the development of multiple organ failure in severe sepsis

Acta Anaesthesiol Scand. 2003 Mar;47(3):319-25. doi: 10.1034/j.1399-6576.2003.00004.x.

Abstract

Background: The production of proinflammatory cytokines activates the systemic inflammatory response in sepsis. Patients also develop a compensatory anti-inflammatory reaction, which may have an important down-regulatory effect on the overactive inflammation. However, the role of this anti-inflammatory response in sepsis is not completely clarified. In this prospective study, we investigated the relationship between the pro- and anti-inflammatory cytokine profiles in severe sepsis and their role in the development of multiple organ failure (MOF).

Methods: Thirty-eight patients meeting the criteria for severe sepsis were studied. MOF was defined as a maximum SOFA score of 10 or higher. Serial measurements of the proinflammatory IL-6 and IL-1beta and the anti-inflammatory IL-10 and IL-1ra were used. The cytokine samples were taken at the onset of sepsis and on the third and fifth day during the ICU period.

Results: The initial IL-10 and IL-1ra responses were identical in patients with or without MOF. The anti-inflammatory cytokine levels remained elevated in the MOF patients, whereas in patients without MOF the levels declined. The IL-6/IL-10 ratio was significantly higher in the MOF patients on days 1 and 3 compared with patients without MOF.

Conclusions: We could not demonstrate overproduction of anti-inflammatory IL-10 in MOF patients. On the contrary, the high IL-6/IL-10 ratio indicates that IL-10 deficiency may contribute to the development of MOF in severe sepsis.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Blood Pressure / drug effects
  • Cardiac Output / drug effects
  • Cytokines / biosynthesis*
  • Female
  • Humans
  • Interleukin-1 / biosynthesis
  • Interleukin-10 / biosynthesis
  • Interleukin-6 / biosynthesis
  • Male
  • Middle Aged
  • Multiple Organ Failure / metabolism*
  • Multiple Organ Failure / microbiology
  • Multiple Organ Failure / physiopathology
  • Oxygen / blood
  • Prospective Studies
  • Sepsis / metabolism*
  • Sepsis / microbiology
  • Sepsis / physiopathology
  • Vascular Resistance / drug effects

Substances

  • Cytokines
  • Interleukin-1
  • Interleukin-6
  • Interleukin-10
  • Oxygen