Vital new insights into deadly African sleeping sickness disease

A newly published extensive body of research into Human African trypanosomiasis (HAT), also known as sleeping sickness, has revealed new insights into the deadly parasitic disease that threatens the lives of millions of people in 36 sub-Saharan African countries. Led by Professor Peter Kennedy CBE in the University of Glasgow and published in PLOS Neglected Tropical Diseases, the research project has found evidence that questions our current understanding of sleeping sickness as a two stage disease - early and late - with direct impact on how we should both diagnose and treat patients with the fatal disease. By using a mouse model of sleeping sickness to better understand how the disease develops, the researchers have been able to show that a range of host genes controlling the development of central nervous system disease are activated much earlier than previously thought, and earlier than the development of neurological features of the disease. These crucial findings could explain why neurological features may occur relatively early in the disease - something that goes against the classical two stage disease understanding - and may also explain why parasites can enter the central nervous system so early after initial infection. Sleeping sickness, is a major killer disease of sub-Saharan Africa which puts around 70 million people at risk in sub-Saharan African countries. Transmitted by tsetse flies when they bite humans to consume a blood meal, and caused by unicellular protozoan parasites called trypanosomes, sleeping sickness is invariably fatal if untreated or inadequately treated.