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The Pathogenesis of African Trypanosomiasis
Etienne Pays1, Magdalena Radwanska2,3, Stefan Magez2,4,5
1Laboratory of Molecular Parasitology, Université Libre de Bruxelles, Gosselies, Belgium;
Annual Review of Pathology
|September 2, 2022
Summary
African trypanosomes cause sleeping sickness by evading the immune system. Specific human apolipoprotein L1 (APOL1) variants protect against this disease but are linked to kidney disease, especially with viral infections.
Area of Science:
- Parasitology
- Immunology
- Genetics
Background:
- African trypanosomes are protozoan parasites causing sleeping sickness in humans and mammals.
- Parasites evade host immune responses for long-term infection and transmission.
- Pathology includes anemia, brain dysfunction, and impaired antibody responses.
Purpose of the Study:
- To investigate the role of apolipoprotein L1 (APOL1) in human resistance to African trypanosomiasis.
- To understand how parasite resistance factors interact with human APOL1.
- To explore the implications of APOL1 variants in disease susceptibility and vaccination.
Main Methods:
- Analysis of host-parasite interactions.
- Study of immune evasion strategies employed by trypanosomes.
- Examination of APOL1 genetic variants and their functional consequences.
Main Results:
- Human serum contains APOL1, a trypanolytic factor.
- Human-infective trypanosomes possess resistance factors inhibiting APOL1.
- Certain human APOL1 variants confer resistance to sleeping sickness by counteracting parasite factors.
Conclusions:
- APOL1 plays a critical role in innate immunity against African trypanosomiasis.
- APOL1 variants offer protection against sleeping sickness but are associated with kidney disease, particularly in inflammatory conditions like COVID-19.
- Understanding these interactions is crucial for developing therapeutic and vaccination strategies.
Keywords:
APOL1African trypanosomesVSGantigenic variationapolipoprotein L1kidney diseasesleeping sicknessvariant surface glycoprotein
