In the first and largest global metabolomic study of African children before and after malaria infection, NYU Abu Dhabi Assistant Professor of Biology Youssef Idaghdour and his colleagues at the Centre National de Recherche et de Formation sur le Paludisme in Burkina Faso have advanced the understanding of the molecular mechanisms in play during human malaria and demonstrated how studying ethnic differences in metabolic responses to the infection can help explain the sources of susceptibility and resistance in this deadly disease.
The study, “Metabolome modulation of the host adaptive immunity in human malaria,” published in the journal Nature Metabolism, provides insight into an area of research previously limited outside of the laboratory setting. Little is known about parasite interactions with the immune system in a living host, especially in children who are the most vulnerable age group to the infection. The team studied blood samples from children from two ethnic groups in remote rural areas of Burkina Faso, Gouin and Fulani, to see how they responded to the malaria parasite Plasmodium falciparum.
The team discovered an elevation of immune-dampening steroid molecules and a strong immunosuppressive signature in Gouin children. Studying the enigmatic, less-malaria-susceptible Fulani ethnic group revealed opposing steroid profiles and stronger immune reactivity to infection.
“The inter-ethnic comparison points to a fundamental molecular mechanism that could define the outcome of the infection in children, and it is fascinating how two human groups could diverge functionally in such a way,” said Idaghdour. “These results will change our understanding of how to achieve better malarial therapeutic interventions and vaccine responsiveness in populations,” added Wael Abdrabou, the first author of the paper.
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