The Pathogenesis of African Trypanosomiasis.

APOL1 African trypanosomes VSG antigenic variation apolipoprotein L1 kidney disease sleeping sickness variant surface glycoprotein

Journal

Annual review of pathology
ISSN: 1553-4014
Titre abrégé: Annu Rev Pathol
Pays: United States
ID NLM: 101275111

Informations de publication

Date de publication:
24 01 2023
Historique:
pubmed: 3 9 2022
medline: 27 1 2023
entrez: 2 9 2022
Statut: ppublish

Résumé

African trypanosomes are bloodstream protozoan parasites that infect mammals including humans, where they cause sleeping sickness. Long-lasting infection is required to favor parasite transmission between hosts. Therefore, trypanosomes have developed strategies to continuously escape innate and adaptive responses of the immune system, while also preventing premature death of the host. The pathology linked to infection mainly results from inflammation and includes anemia and brain dysfunction in addition to loss of specificity and memory of the antibody response. The serum of humans contains an efficient trypanolytic factor, the membrane pore-forming protein apolipoprotein L1 (APOL1). In the two human-infective trypanosomes, specific parasite resistance factors inhibit APOL1 activity. In turn, many African individuals express APOL1 variants that counteract these resistance factors, enabling them to avoid sleeping sickness. However, these variants are associated with chronic kidney disease, particularly in the context of virus-induced inflammation such as coronavirus disease 2019. Vaccination perspectives are discussed.

Identifiants

pubmed: 36055769
doi: 10.1146/annurev-pathmechdis-031621-025153
doi:

Substances chimiques

APOL1 protein, human 0
Apolipoprotein L1 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

19-45

Auteurs

Etienne Pays (E)

Laboratory of Molecular Parasitology, Université Libre de Bruxelles, Gosselies, Belgium; email: etienne.pays@ulb.be.

Magdalena Radwanska (M)

Laboratory for Biomedical Research, Ghent University Global Campus, Incheon, South Korea.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; email: Magdalena.Radwanska@ghent.ac.kr.

Stefan Magez (S)

Laboratory for Biomedical Research, Ghent University Global Campus, Incheon, South Korea.
Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium; email: Stefan.Magez@vub.be.
Department of Biochemistry and Microbiology, Ghent University, Ghent, Belgium.

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Classifications MeSH