Last Updated: 02/09/2025
The malaria zoo: dissecting cerebral malaria in three in vitro primate blood-brain barrier models (MAL-ZOO)
Objectives
The MAL-ZOO project aims to test the hypotheses that the pathogenic mechanisms of cerebral malaria (CM) in primates are host and parasite-specific. MAL-ZOO will develop innovative microvascular 3D in vitro models using induced pluripotent stem cell technology for the cross-species comparison of the virulence factors during infections.
Plasmodium falciparum cerebral malaria (CM) is the most severe complication during malaria infections. CM is associated with patient coma and blood-brain barrier (BBB) disruption resulting in brain swelling and patient death. In the zoonotic malaria parasite P. knowlesi, CM is described in rhesus macaques but occurs neither in human infections nor in the natural long-tail macaque reservoir. Infected red blood cell cytoadhesion to endothelial cells and the release of parasite toxins have been described as pathogenic mechanisms of falciparum CM. Both factors are present in P. knowlesi in all three primate hosts, albeit at different levels and result in different clinical outcomes. Therefore, the hypothesis is that the pathogenic mechanisms of CM in primates are host and parasite-specific.
As in vivo studies are limited to post mortem samples, the aim is to develop in MAL-ZOO novel microvascular 3D in vitro models of the human, rhesus macaque and long tail macaque BBB. Existing differentiation protocols for human induced pluripotent stem cells (iPSC) will be adapted to generate macaque endothelial cells, astrocytes and pericytes, that will be introduced in a 3D microvascular model. Taking advantage of the microfluidic properties of the devices, the dynamics of P. knowlesi cytoadhesion will be characterized to the endothelium of the three hosts. Afterwards, the BBB pathogenicity of these two parasites will be measured by confocal microscopy, functional permeability assays and RNAseq transcriptional analysis and correlate it to the parasite cytoadhesion levels. The cross-species comparison will be used to highlight species-specific virulence factors during P. falciparum and P. knowlesi infections. This will improve understanding of the mechanisms leading to P. falciparum CM in humans and the pathogenic potential of zoonotic P. knowlesi malaria.
Apr 2023 — Mar 2025
$183,665
