Adenovirus serotype 5-vectored foot-and-mouth disease subunit vaccines: the first decade

Author:

Grubman Marvin J1,Moraes Mauro P2,Schutta Christopher3,Barrera Jose4,Neilan John3,Ettyreddy Damodar5,Butman Bryan T5,Brough Douglas E5,Brake David A6

Affiliation:

1. USDA, ARS, NAA, Plum Island Animal Disease Center, PO Box 848, Greenport, NY 11944, USA.

2. Plum Island Animal Disease Center, North Atlantic Area, Agricultural Research Service, US Department of Agriculture, Greenport, NY 11944, USA.

3. Plum Island Animal Disease Center, Department of Homeland Security, Science & Technology Directorate, Greenport, NY 11944, USA.

4. The McConnell Group, Inc., Dublin, PA 18917, USA.

5. GenVec, Inc., Gaithersburg, MD 20878, USA.

6. BioQuest Associates LLC, East Lyme, CT 06333, USA.

Abstract

The results of the first decade of the development of a replication-defective human adenovirus serotype 5 (Ad5) containing the capsid- and 3C protease-coding regions of foot-and-mouth disease (FMD) virus as a vaccine candidate are presented. In proof-of-concept studies, it was demonstrated that a single inoculation with this vaccine vector containing the capsid of FMD virus A24 Cruzeiro protected both swine and cattle following homologous challenge by direct inoculation 1 week postvaccination. We have expanded these studies in cattle with larger numbers of animals and by testing the vaccine in direct-contact challenge studies, including its ability to prevent FMD virus shedding and transmission. Furthermore, we have developed manufacturing protocols to allow the scalable production of these FMD molecular vaccine products for US Department of Agriculture licensure approval and availability for inclusion in the US National Veterinary Stockpile. We have also constructed and initiated cattle efficacy testing of Ad5 vectors containing the capsid-coding regions from other FMD virus serotypes and subtypes, as well as initiated studies to improve FMD molecular vaccine potency.

Publisher

Future Medicine Ltd

Subject

Virology

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