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DNA ME-TRAP + MVA ME-TRAP is an investigational heterologous prime-boost malaria vaccine regimen. It consists of two distinct components: a plasmid DNA priming vaccine and a Modified Vaccinia virus Ankara (MVA) boosting vaccine. Both components encode the same recombinant antigen, ME-TRAP, which is a fusion of a multiple epitope (ME) string and the Thrombospondin-Related Adhesion Protein (TRAP) from the pre-erythrocytic sporozoite stage of *Plasmodium falciparum*. The regimen is designed to induce high-frequency effector T cell responses (specifically CD8+ and CD4+ T cells) against the liver stage of the malaria parasite to prevent progression to symptomatic disease. Developed by the London School of Hygiene and Tropical Medicine in collaboration with the University of Oxford, the vaccine was evaluated in clinical trials in West Africa but failed to demonstrate significant protective efficacy against natural infection in semi-immune adults.
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