A complex adenovirus-vectored vaccine against Rift Valley fever virus protects mice against lethal infection in the presence of preexisting vector immunity

Clin Vaccine Immunol. 2009 Nov;16(11):1624-32. doi: 10.1128/CVI.00182-09. Epub 2009 Sep 23.

Abstract

Rift Valley fever virus (RVFV) has been cited as a potential biological-weapon threat due to the serious and fatal disease it causes in humans and animals and the fact that this mosquito-borne virus can be lethal in an aerosolized form. Current human and veterinary vaccines against RVFV, however, are outdated, inefficient, and unsafe. We have incorporated the RVFV glycoprotein genes into a nonreplicating complex adenovirus (CAdVax) vector platform to develop a novel RVFV vaccine. Mice vaccinated with the CAdVax-based vaccine produced potent humoral immune responses and were protected against lethal RVFV infection. Additionally, protection was elicited in mice despite preexisting immunity to the adenovirus vector.

MeSH terms

  • Adenoviridae / genetics*
  • Animals
  • Antibodies, Viral / blood
  • Genetic Vectors*
  • Male
  • Mice
  • Rift Valley Fever / immunology
  • Rift Valley Fever / prevention & control*
  • Rift Valley fever virus / genetics
  • Rift Valley fever virus / immunology*
  • Survival Analysis
  • Viral Structural Proteins / genetics
  • Viral Structural Proteins / immunology
  • Viral Vaccines / genetics
  • Viral Vaccines / immunology*

Substances

  • Antibodies, Viral
  • Viral Structural Proteins
  • Viral Vaccines