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FP9 ME-TRAP is a candidate malaria vaccine developed at the University of Oxford. It uses a highly attenuated fowlpox virus vector (FP9) to deliver the multiple epitope-thrombospondin-related adhesion protein (ME-TRAP) antigen, which is designed to induce strong cellular immune responses, particularly CD8+ T cell responses, against pre-erythrocytic stages of *Plasmodium falciparum*. The ME string includes multiple T and B cell epitopes from several malaria antigens fused to TRAP. FP9 ME-TRAP has been evaluated in prime–boost regimens with other viral vectors such as MVA (modified vaccinia Ankara), aiming to enhance immunogenicity and protection against malaria infection. Clinical trials have shown that while the vaccine can induce immune responses, efficacy in preventing clinical malaria has been limited[2][5][6][7][8].
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