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HSV-1 amplicon vectors that direct the in situ production of foot-and-mouth disease virus antigens in mammalian cells can be used for genetic immunization.

Abstract
HSV-1 amplicon vectors encoding heterologous antigens were capable to mediate in situ generation of protein synthesis and to generate a specific immune response to the corresponding antigens. In this study, foot-and-mouth disease (FMD) virus antigens were used to generate a genetic vaccine prototype. The amplicons were designed to provide a high safety profile as they do not express any HSV-1 genes when packaged using a helper virus-free system, and they are able to encapsidate several copies of the transgene or allow the simultaneous expression of different genes. Virus-like particles were produced after cell processing of the delivered DNA. Inoculation of mice with 5 × 10(5) transducing units of amplicon vectors resulted in FMDV-specific humoral responses in the absence of adjuvants, which were dependent on the in situ de novo production of the vector-encoded antigens. Challenge of mice vaccinated with these amplicons with a high dose of live virus, resulted in partial protection, with a significant reduction of viremia. This work highlights the potential use of a HSV-1 amplicon vector platform for generation of safe genetic vaccines.
AuthorsAlejandra D'Antuono, Andrea S Laimbacher, Jose La Torre, Virginia Tribulatti, Carina Romanutti, Patricia Zamorano, Valeria Quattrocchi, Elisabeth M Schraner, Mathias Ackermann, Cornel Fraefel, Nora Mattion
JournalVaccine (Vaccine) Vol. 28 Issue 46 Pg. 7363-72 (Oct 28 2010) ISSN: 1873-2518 [Electronic] Netherlands
PMID20851082 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2010 Elsevier Ltd. All rights reserved.
Chemical References
  • Antibodies, Viral
  • Antigens, Viral
  • Capsid Proteins
  • Vaccines, DNA
  • Viral Vaccines
Topics
  • Animals
  • Antibodies, Viral (blood)
  • Antigens, Viral (biosynthesis, immunology)
  • Capsid Proteins (biosynthesis, immunology)
  • Chlorocebus aethiops
  • Foot-and-Mouth Disease (immunology, prevention & control)
  • Foot-and-Mouth Disease Virus (genetics, immunology)
  • Genetic Vectors
  • HEK293 Cells
  • Herpesvirus 1, Human (immunology)
  • Humans
  • Mice
  • Mice, Inbred BALB C
  • Transgenes
  • Vaccines, DNA (biosynthesis, immunology)
  • Vero Cells
  • Viral Vaccines (biosynthesis, immunology)

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