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Vaccine-mediated protection of pigs against infection with pandemic H1N1 2009 swine influenza A virus requires a close antigenic match between the vaccine antigen and challenge virus
Authors:Helen E. Everett  Mario Aramouni  Vivien Coward  Andrew Ramsay  Michael Kelly  Sophie Morgan  Elma Tchilian  Laetitia Canini  Mark E.J. Woolhouse  Sarah Gilbert  Bryan Charleston  Ian H. Brown  Sharon M. Brookes
Affiliation:1. Virology Department, Animal and Plant Health Agency (APHA-Weybridge), New Haw, Addlestone KT15 3NB, UK;2. The Jenner Institute, University of Oxford, ORCRB, Roosevelt Drive, Oxford OX3 7DQ, UK;3. University of Edinburgh, Charlotte Auerbach Road, Edinburgh EH9 3FL, UK;4. The Pirbright Institute, Ash Road, Pirbright, Woking GU24 0NF, UK
Abstract:Swine influenza A virus (SwIV) infection has considerable economic and animal welfare consequences and, because of the zoonotic potential, can also have public health implications. The 2009 pandemic H1N1 ‘swine-origin’ infection is now endemic in both pigs and humans. In Europe, avian-like H1avN1, human-like H1huN2, human-like swine H3N2 and, since 2009, pandemic H1N1 (pH1N1) lineage viruses and reassortants, constitute the dominant subtypes. In this study, we used a swine pH1N1 challenge virus to investigate the efficacy of whole inactivated virus vaccines homologous or heterologous to the challenge virus as well as a commercial vaccine. We found that vaccine-mediated protection was most effective when vaccine antigen and challenge virus were homologous and correlated with the specific production of neutralising antibodies and a cellular response to the challenge virus. We conclude that a conventional whole inactivated SwIV vaccine must be antigenically matched to the challenge strain to be an effective control measure.
Keywords:Swine influenza A virus  Pandemic 2009 influenza A virus  H1N1  Whole inactivated virus vaccine  Immune response
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