Glucuronoxylomannan, the major capsular polysaccharide of Cryptococcus neoformans, inhibits the progression of group B streptococcal arthritis

Infect Immun. 2004 Nov;72(11):6367-72. doi: 10.1128/IAI.72.11.6367-6372.2004.

Abstract

Glucuronoxylomannan (GXM), the principal constituent of the Cryptococcus neoformans capsule, modulates the inflammatory response of human monocytes in vitro. Here we examine the efficacy of GXM as a novel anti-inflammatory compound for use against experimental septic arthritis. Arthritis was induced in mice by the intravenous injection of 8 x 10(6) CFU of type IV group B streptococcus (GBS). GXM was administered intravenously in different doses (50, 100, or 200 microg/mouse) 1 day before and 1 day after bacterial inoculation. GXM treatment markedly decreased the incidence and severity of articular lesions. Histological findings showed limited periarticular inflammation in the joints of GXM-treated mice, confirming the clinical observations. The amelioration of arthritis was associated with a significant reduction in the local production of interleukin-6 (IL-6), IL-1beta, macrophage inflammatory protein 1alpha (MIP-1alpha), and MIP-2 and an increase in systemic IL-10 levels. Moreover, peritoneal macrophages derived from GXM-treated mice and stimulated in vitro with heat-inactivated GBS showed a similar pattern of cytokine production. The present study provides evidence for the modulation of the inflammatory response by GXM in vivo and suggests a potential therapeutic use for this compound in pathologies involving inflammatory processes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Outbred Strains
  • Arthritis, Infectious / drug therapy*
  • Arthritis, Infectious / immunology
  • Arthritis, Infectious / mortality
  • Arthritis, Infectious / pathology
  • Cryptococcus neoformans / chemistry*
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Mice
  • Polysaccharides / administration & dosage
  • Polysaccharides / therapeutic use*
  • Severity of Illness Index
  • Streptococcal Infections / drug therapy*
  • Streptococcal Infections / immunology
  • Streptococcal Infections / mortality
  • Streptococcal Infections / pathology
  • Streptococcus agalactiae / drug effects*
  • Streptococcus agalactiae / pathogenicity
  • Treatment Outcome

Substances

  • Cytokines
  • Polysaccharides
  • glucuronoxylomannan