Glycolipids are potential targets for protozoan parasite diseases

Trends Parasitol. 2010 Aug;26(8):404-11. doi: 10.1016/j.pt.2010.04.006. Epub 2010 May 17.

Abstract

Induction of sterilizing immunity by vaccination is extremely difficult because of the evasion mechanisms developed by parasites, and identification of new targets for therapy is therefore important. Glycosylphosphatidylinositols (GPIs) of parasites are glycolipids that participate in pathogenicity of parasitic diseases. Studies of Plasmodium falciparum and Trypanosoma brucei indicate that GPIs are good candidates for developing vaccines against malaria and sleeping sickness, respectively. By contrast, fatty acids isolated from P. falciparum and Toxoplasma gondii can inhibit the production of inflammatory cytokines induced by the GPIs in macrophages. GPIs are considered to be toxins that, if present in large amounts, induce irreversible damages to the host, and treatment with fatty acids could reduce this effect.

Publication types

  • Review

MeSH terms

  • Adult
  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / therapeutic use*
  • CHO Cells
  • Child
  • Cricetinae
  • Cricetulus
  • Cytokines / metabolism
  • Fatty Acids / pharmacology
  • Fatty Acids / therapeutic use*
  • Glycosylphosphatidylinositols / biosynthesis*
  • Glycosylphosphatidylinositols / chemistry
  • Glycosylphosphatidylinositols / immunology
  • Humans
  • Inflammation / drug therapy
  • Macrophages / immunology
  • Mice
  • Plasmodium falciparum / drug effects
  • Plasmodium falciparum / immunology
  • Protozoan Infections / drug therapy*
  • Protozoan Infections / parasitology
  • Toxoplasma / drug effects
  • Toxoplasma / immunology

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Fatty Acids
  • Glycosylphosphatidylinositols