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Immunogenicity of dengue virus type 1 DNA vaccines expressing truncated and full length envelope protein
Authors:Raviprakash K  Kochel T J  Ewing D  Simmons M  Phillips I  Hayes C G  Porter K R
Affiliation:Virology Program, Infectious Diseases Department, Naval Medical Research Institute, 8901 Wisconsin Avenue, Bethesda, MD, USA. ravik@nmripo.nmri.nnmc.navy.mil
Abstract:Recombinant plasmid DNA constructs expressing truncated or full-length dengue-1 envelope (E) with or without the pre-membrane (prM) were tested for immunogenicity in mice, as candidate dengue DNA vaccines. Two plasmids, one expressing the N-terminal 80% E and the other expressing prM and full length E were immunogenic in intradermally inoculated mice. The vaccinated mice produced dengue-1 specific antibodies that were both neutralizing and long lasting. Data suggested that the plasmid expressing prM and full length E produced virus like particles in transfected cells, and is probably a better immunogen compared to that expressing 80% E.
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