Intra-abdominal sepsis alters tumor necrosis factor-alpha and interleukin-1 beta binding to human neutrophils

Crit Care Med. 1992 Jan;20(1):11-6. doi: 10.1097/00003246-199201000-00009.

Abstract

Objective: To determine the effects of intraabdominal sepsis on polymorphonuclear leukocyte tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta) receptor expression.

Design: Prospective, randomized comparison between patients undergoing elective colon surgery vs. patients with intra-abdominal sepsis.

Setting: Tertiary-care center with all patients with intra-abdominal sepsis in a surgical ICU environment.

Patients: Group 1 (n = 7) represents control patients who underwent elective colon surgery without intra-abdominal sepsis. Group 2 (n = 10) represents patients with intra-abdominal sepsis.

Measurements and main results: Polymorphonuclear leukocyte TNF-alpha and IL-1 beta receptor expression +/- stimulation of the oxidative burst was measured using 125I TNF-alpha and 125I IL-1 beta. Superoxide anion production and candicidal activity were measured in the presence of TNF-alpha and IL-1 beta. Group 2 patients expressed fewer TNF-alpha and IL-1 beta receptors on their cell surface, and stimulation of oxidative burst reduced TNF-alpha and IL-1 beta receptor expression in group 2 more than in group 1. Diminished TNF-alpha and IL-1 beta binding reduced superoxide anion production by group 2 polymorphonuclear leukocytes. Decreased TNF-alpha binding but not IL-1 beta, reduced polymorphonuclear leukocyte candicidal activity by group 2 polymorphonuclear leukocytes.

Conclusions: a) Intra-abdominal sepsis reduces polymorphonuclear leukocyte TNF-alpha and IL-1 beta receptor expression. b) Expression of these surface receptors is altered by stimulation of the polymorphonuclear leukocyte oxidative burst. c) Diminished TNF-alpha and IL-1 beta receptor expression is associated with functional impairments in polymorphonuclear leukocyte activity.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Abdomen*
  • Aged
  • Female
  • Gram-Negative Bacterial Infections / immunology
  • Gram-Negative Bacterial Infections / metabolism*
  • Humans
  • Immune Tolerance
  • Interleukin-1 / immunology
  • Interleukin-1 / metabolism*
  • Ligands
  • Male
  • Middle Aged
  • Neutrophils / immunology
  • Neutrophils / metabolism*
  • Prospective Studies
  • Receptors, Cell Surface / biosynthesis*
  • Receptors, Cell Surface / immunology
  • Receptors, Cell Surface / metabolism
  • Receptors, Immunologic / biosynthesis*
  • Receptors, Immunologic / immunology
  • Receptors, Immunologic / metabolism
  • Receptors, Interleukin-1
  • Receptors, Tumor Necrosis Factor
  • Respiratory Burst / immunology
  • Superoxides / metabolism
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Interleukin-1
  • Ligands
  • Receptors, Cell Surface
  • Receptors, Immunologic
  • Receptors, Interleukin-1
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha
  • Superoxides