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Last Updated: 19/06/2024
Dissecting how the NLRP3 inflammasome provokes blood brain barrier dysfunction during cerebral malaria
Objectives
This project will use a murine model of CM (experimental cerebral malaria; ECM), which we has been validated, and a combination of imaging, biochemical, and immunological techniques to determine the temporal and spatial regulation of NLRP3 inflammasome activation, the proximity of this event to areas of blood-brain barrier disruption, and how NLRP3-dependent inflammation signals to affect vasogenic oedema.
Diseases caused by parasites have devastating consequences on the human population. The most important disease caused by a parasite is malaria which causes over 400,000 deaths every year. One of the most devastating consequences of malaria is a syndrome called cerebral malaria. Cerebral malaria is where the disease has affected the brain. The outcome of cerebral malaria, which is most prevalent in children, is death, caused by swelling of the brain. This swelling occurs because the barrier between the blood and the brain breaks down. The integrity of this ‘blood-brain barrier’ is critical for normal brain function and survival. Recent research has provided good clues to how the blood-brain barrier breaks down in cerebral malaria. The main culprit are the own immune systems that are activated by the disease and turn against our own bodies. A specific part of the immune system, called the ‘NLRP3 inflammasome’ becomes active to break the blood-brain barrier. If it could be understood how, when, and where this happens it will help to develop ways of blocking the NLRP3 inflammasome and its effects. If this can be done then this might enable better treatment of cerebral malaria, and ultimately prevent the deaths of hundreds of thousands of children every year. This research may also be relevant to other diseases where the blood-brain barrier is compromised.
Dec 2022 — Nov 2025
$743,733