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Clinical and Vaccine Immunology, November 2009, p. 1624-1632, Vol. 16, No. 11
1071-412X/09/$08.00+0 doi:10.1128/CVI.00182-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

GenPhar, Inc., Division of Biodefense Vaccines, 600 Seacoast Pkwy., Mount Pleasant, South Carolina 29464,1 University of Texas Medical Branch, Department of Pathology, 301 University Blvd., Galveston, Texas 77555-0609,2 Medical University of South Carolina, Department of Microbiology and Immunology, 171 Ashley Avenue, BSB201, Charleston, South Carolina 294033
Received 6 May 2009/ Returned for modification 22 June 2009/ Accepted 8 September 2009
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 Current human and veterinary vaccines against RVFV, however, are outdated, inefficient, and unsafe.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.
Published ahead of print on 23 September 2009.
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