Genetic and immunological basis of human African trypanosomiasis

Curr Opin Immunol. 2021 Oct:72:13-20. doi: 10.1016/j.coi.2021.02.007. Epub 2021 Mar 12.

Abstract

Human African trypanosomiasis, or sleeping sickness, results from infection by two subspecies of the protozoan flagellate parasite Trypanosoma brucei, termed Trypanosoma brucei gambiense and Trypanosoma brucei rhodesiense, prevalent in western and eastern Africa respectively. These subspecies escape the trypanolytic potential of human serum, which efficiently acts against the prototype species Trypanosoma brucei brucei, responsible for the Nagana disease in cattle. We review the various strategies and components used by trypanosomes to counteract the immune defences of their host, highlighting the adaptive genomic evolution that occurred in both parasite and host to take the lead in this battle. The main parasite surface antigen, named Variant Surface Glycoprotein or VSG, appears to play a key role in different processes involved in the dialogue with the host.

Publication types

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

MeSH terms

  • Adaptive Immunity
  • Apolipoprotein L1 / genetics
  • Apolipoprotein L1 / metabolism
  • Disease Resistance / genetics
  • Disease Resistance / immunology
  • Disease Susceptibility / immunology*
  • Gene Expression Regulation
  • Genetic Predisposition to Disease*
  • Genetic Variation
  • Host-Parasite Interactions / genetics
  • Host-Parasite Interactions / immunology
  • Humans
  • Immunity, Innate
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Protein Binding
  • Protozoan Proteins / genetics
  • Protozoan Proteins / immunology
  • Protozoan Proteins / metabolism
  • Trypanosoma brucei gambiense / immunology
  • Trypanosomiasis, African / etiology*
  • Trypanosomiasis, African / metabolism

Substances

  • APOL1 protein, human
  • Apolipoprotein L1
  • Membrane Glycoproteins
  • Protozoan Proteins