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Immunogenicity of chimeric hemagglutinins delivered by an orf virus vector platform against swine influenza virus. | LitMetric

Immunogenicity of chimeric hemagglutinins delivered by an orf virus vector platform against swine influenza virus.

Front Immunol

Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, United States.

Published: March 2024

AI Article Synopsis

  • Orf virus (ORFV) is utilized as a vector to deliver chimeric hemagglutinins (HAs) of Influenza A virus in pigs, addressing the challenge of strain-specific immunity in vaccine development.
  • Researchers created two recombinant ORFVs expressing HAs that include a common stalk from a contemporary H1N1 strain along with different exotic head domains (H6 and H8).
  • After vaccination, piglets showed enhanced antibody responses, indicating strong immune responses, and reduced viral shedding when challenged with divergent IAV-S strains, highlighting the potential effectiveness of ORFV-based vaccines.

Article Abstract

Orf virus (ORFV) is a large DNA virus that can harbor and efficiently deliver viral antigens in swine. Here we used ORFV as a vector platform to deliver chimeric hemagglutinins (HA) of Influenza A virus of swine (IAV-S). Vaccine development against IAV-S faces limitations posed by strain-specific immunity and the antigenic diversity of the IAV-S strains circulating in the field. A promising alternative aiming at re-directing immune responses on conserved epitopes of the stalk segment of the hemagglutinin (HA2) has recently emerged. Sequential immunization with chimeric HAs comprising the same stalk but distinct exotic head domains can potentially induce cross-reactive immune responses against conserved epitopes of the HA2 while breaking the immunodominance of the head domain (HA1). Here, we generated two recombinant ORFVs expressing chimeric HAs encoding the stalk region of a contemporary H1N1 IAV-S strain and exotic heads derived from either H6 or H8 subtypes, ORFVcH6/1 and ORFVcH8/1, respectively. The resulting recombinant viruses were able to express the heterologous protein . Further, the immunogenicity and cross-protection of these vaccine candidates were assessed in swine after sequential intramuscular immunization with OV-cH6/1 and OV-cH8/1, and subsequent challenge with divergent IAV-S strains. Humoral responses showed that vaccinated piglets presented increasing IgG responses in sera. Additionally, cross-reactive IgG and IgA antibody responses elicited by immunization were detected in sera and bronchoalveolar lavage (BAL), respectively, by ELISA against different viral clades and a diverse range of contemporary H1N1 IAV-S strains, indicating induction of humoral and mucosal immunity in vaccinated animals. Importantly, viral shedding was reduced in nasal swabs from vaccinated piglets after intranasal challenge with either Oh07 (gamma clade) or Ca09 (npdm clade) IAV-S strains. These results demonstrated the efficiency of ORFV-based vectors in delivering chimeric IAV-S HA-based vaccine candidates and underline the potential use of chimeric-HAs for prevention and control of influenza in swine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10933025PMC
http://dx.doi.org/10.3389/fimmu.2024.1322879DOI Listing

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