Abstract
Protein-in-adjuvant vaccines have shown limited success against difficult diseases such as blood-stage malaria. Here we show that a recombinant adenovirus-poxvirus prime-boost immunization regime (known to induce strong T cell immunogenicity) can also induce very strong antigen-specific antibody responses, and we identify a simple complement-based adjuvant to further enhance immunogenicity. Antibodies induced against a blood-stage malaria antigen by this viral vector platform are highly effective against Plasmodium yoelii parasites in mice and against Plasmodium falciparum in vitro.
Publication types
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Research Support, N.I.H., Intramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenoviridae / chemistry
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Animals
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Genetic Vectors / chemistry*
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Immunoglobulin G / chemistry
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Malaria / prevention & control
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Malaria Vaccines / chemistry*
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Mice
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Mice, Inbred BALB C
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Plasmodium falciparum / metabolism
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Plasmodium yoelii / metabolism
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Poxviridae / chemistry
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T-Lymphocytes / parasitology
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T-Lymphocytes / virology*
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Vaccines / chemistry
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Vaccines, Subunit / chemistry
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Viral Vaccines / chemistry*
Substances
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Immunoglobulin G
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Malaria Vaccines
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Vaccines
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Vaccines, Subunit
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Viral Vaccines