DNA Vaccination Elicits Protective Immune Responses against Pandemic and Classic Swine Influenza Viruses in Pigs

Author:

Gorres J. Patrick1,Lager Kelly M.2,Kong Wing-Pui3,Royals Michael4,Todd John-Paul1,Vincent Amy L.2,Wei Chih-Jen3,Loving Crystal L.2,Zanella Eraldo L.5,Janke Bruce6,Kehrli Marcus E.2,Nabel Gary J.3,Rao Srinivas S.1

Affiliation:

1. Laboratory Animal Medicine, Vaccine Research Center, National Institutes of Health, Bethesda, Maryland 20892

2. Virus and Prion Diseases Research Unit, National Animal Disease Center, U.S. Department of Agriculture Agricultural Research Service, Ames, Iowa 50010

3. Vector Core, Vaccine Research Center, National Institutes of Health, Bethesda, Maryland 20892

4. PharmaJet, Inc., Golden, Colorado 80401

5. Universidade de Passo Fundo, Curso de Medicina Veterinária, Campus Universitário do Bairro São José, Caixa Postal 611, Passo Fundo RS 99001-970, Brazil

6. Iowa State University College of Veterinary Medicine, Vet Diagnostic and Production Animal Med, 1657 Vet Med, Ames, Iowa 50011

Abstract

ABSTRACT Swine influenza is a highly contagious viral infection in pigs that significantly impacts the pork industry due to weight loss and secondary infections. There is also the potential of a significant threat to public health, as was seen in 2009 when the pandemic H1N1 influenza virus strain emerged from reassortment events among avian, swine, and human influenza viruses within pigs. As classic and pandemic H1N1 strains now circulate in swine, an effective vaccine may be the best strategy to protect the pork industry and public health. Current inactivated-virus vaccines available for swine influenza protect only against viral strains closely related to the vaccine strain, and egg-based production of these vaccines is insufficient to respond to large outbreaks. DNA vaccines are a promising alternative since they can potentially induce broad-based protection with more efficient production methods. In this study we evaluated the potentials of monovalent and trivalent DNA vaccine constructs to (i) elicit both humoral and gamma interferon (IFN-γ) responses and (ii) protect pigs against viral shedding and lung disease after challenge with pandemic H1N1 or classic swine H1N1 influenza virus. We also compared the efficiency of a needle-free vaccine delivery method to that of a conventional needle/syringe injection. We report that DNA vaccination elicits robust serum antibody and cellular responses after three immunizations and confers significant protection against influenza virus challenge. Needle-free delivery elicited improved antibody responses with the same efficiency as conventional injection and should be considered for development as a practical alternative for vaccine administration.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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