Bovine dialyzable leukocyte extract protects against LPS-induced, murine endotoxic shock

Int Immunopharmacol. 2004 Dec 15;4(13):1577-86. doi: 10.1016/j.intimp.2004.06.014.

Abstract

The pathophysiology of endotoxic shock is characterized by the activation of multiple pro-inflammatory genes and their products which initiate the inflammatory process. Endotoxic shock is a serious condition with high mortality. Bovine dialyzable leukocyte extract (bDLE) is a dialyzate of a heterogeneous mixture of low molecular weight substances released from disintegrated leukocytes of the blood or lymphoid tissue obtained from homogenized bovine spleen. bDLE is clinically effective for a broad spectrum of diseases. To determine whether bDLE improves survival and modulates the expression of pro-inflammatory cytokine genes in LPS-induced, murine endotoxic shock, Balb/C mice were treated with bDLE (1 U) after pretreatment with LPS (17 mg/kg). The bDLE improved survival (90%), suppressed IL-10 and IL-6, and decreased IL-1beta, TNF-alpha, and IL-12p40 mRNA expression; and decreased the production of IL-10 (P<0.01), TNF-alpha (P<0.01), and IL-6 (P<0.01) in LPS-induced, murine endotoxic shock. Our results demonstrate that bDLE leads to improved survival in LPS-induced endotoxic shock in mice, modulating the pro-inflammatory cytokine gene expression, suggesting that bDLE is an effective therapeutic agent for inflammatory illnesses associated with an unbalanced expression of pro-inflammatory cytokine genes such as in endotoxic shock, rheumatic arthritis and other diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cytokines / classification
  • Cytokines / genetics
  • Cytokines / immunology
  • Dose-Response Relationship, Drug
  • Endotoxins / adverse effects*
  • Endotoxins / antagonists & inhibitors
  • Inflammation / genetics
  • Inflammation / immunology
  • Inflammation Mediators / immunology
  • Inflammation Mediators / metabolism
  • Injections, Intraperitoneal
  • Leukocytes / immunology
  • Lipopolysaccharides / adverse effects*
  • Lipopolysaccharides / antagonists & inhibitors*
  • Mexico
  • Mice
  • Mice, Inbred BALB C
  • Shock, Septic / chemically induced
  • Shock, Septic / mortality*
  • Shock, Septic / prevention & control*
  • Transfer Factor / pharmacology
  • Transfer Factor / therapeutic use*

Substances

  • Cytokines
  • Endotoxins
  • Inflammation Mediators
  • Lipopolysaccharides
  • Transfer Factor