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A heterologous prime-boost malaria vaccine regimen targeting the blood-stage Plasmodium falciparum parasite. It consists of a chimpanzee adenovirus vector (AdCh63/ChAd63) expressing MSP1 for priming, followed by a modified vaccinia virus Ankara (MVA) vector expressing the same MSP1 antigen for boosting. The MSP1 antigen is designed with conserved blocks of sequence and two divergent allelic sequences to address antigenic polymorphism and induce strain-transcending immunity.
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