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pubmed-article:12766765pubmed:abstractTextIn animals, effective immune responses against malignancies and against several infectious pathogens, including malaria, are mediated by T cells. Here we show that a heterologous prime-boost vaccination regime of DNA either intramuscularly or epidermally, followed by intradermal recombinant modified vaccinia virus Ankara (MVA), induces high frequencies of interferon (IFN)-gamma-secreting, antigen-specific T-cell responses in humans to a pre-erythrocytic malaria antigen, thrombospondin-related adhesion protein (TRAP). These responses are five- to tenfold higher than the T-cell responses induced by the DNA vaccine or recombinant MVA vaccine alone, and produce partial protection manifest as delayed parasitemia after sporozoite challenge with a different strain of Plasmodium falciparum. Such heterologous prime-boost immunization approaches may provide a basis for preventative and therapeutic vaccination in humans.lld:pubmed
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pubmed-article:12766765pubmed:articleTitleEnhanced T-cell immunogenicity of plasmid DNA vaccines boosted by recombinant modified vaccinia virus Ankara in humans.lld:pubmed
pubmed-article:12766765pubmed:affiliationNuffield Department of Medicine, University of Oxford, John Radcliffe Hospital, Oxford, OX3 9DU, UK.lld:pubmed
pubmed-article:12766765pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12766765pubmed:publicationTypeClinical Triallld:pubmed
pubmed-article:12766765pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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