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Evaluation of hydrophobic chitosan-based particulate formulations of porcine reproductive and respiratory syndrome virus vaccine candidate T cell antigens.
Mokhtar, Helen; Biffar, Lucia; Somavarapu, Satyanarayana; Frossard, Jean-Pierre; McGowan, Sarah; Pedrera, Miriam; Strong, Rebecca; Edwards, Jane C; Garcia-Durán, Margarita; Rodriguez, Maria Jose; Stewart, Graham R; Steinbach, Falko; Graham, Simon P.
Afiliación
  • Mokhtar H; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom; Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, United Kingdom.
  • Biffar L; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom.
  • Somavarapu S; School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, United Kingdom.
  • Frossard JP; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom.
  • McGowan S; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom.
  • Pedrera M; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom.
  • Strong R; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom.
  • Edwards JC; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom.
  • Garcia-Durán M; Ingenasa, C/Hermanos García Noblejas, 41, 2° Madrid, 28037, Spain.
  • Rodriguez MJ; Ingenasa, C/Hermanos García Noblejas, 41, 2° Madrid, 28037, Spain.
  • Stewart GR; Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, United Kingdom.
  • Steinbach F; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom; Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, United Kingdom.
  • Graham SP; Virology Department, Animal and Plant Health Agency, Addlestone, KT15 3NB, United Kingdom; Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, United Kingdom. Electronic address: simon.graham@pirbright.ac.uk.
Vet Microbiol ; 209: 66-74, 2017 Sep.
Article en En | MEDLINE | ID: mdl-28228336
PRRS control is hampered by the inadequacies of existing vaccines to combat the extreme diversity of circulating viruses. Since immune clearance of PRRSV infection may not be dependent on the development of neutralising antibodies and the identification of broadly-neutralising antibody epitopes have proven elusive, we hypothesised that conserved T cell antigens represent potential candidates for development of a novel PRRS vaccine. Previously we had identified the M and NSP5 proteins as well-conserved targets of polyfunctional CD8 and CD4 T cells. To assess their vaccine potential, peptides representing M and NSP5 were encapsulated in hydrophobically-modified chitosan particles adjuvanted by incorporation of a synthetic multi-TLR2/TLR7 agonist and coated with a model B cell PRRSV antigen. For comparison, empty particles and adjuvanted particles encapsulating inactivated PRRSV-1 were prepared. Vaccination with the particulate formulations induced antigen-specific antibody responses, which were most pronounced following booster immunisation. M and NSP5-specific CD4, but not CD8, T cell IFN-γ reactivity was measurable following the booster immunisation in a proportion of animals vaccinated with peptide-loaded particles. Upon challenge, CD4 and CD8 T cell reactivity was detected in all groups, with the greatest responses being detected in the peptide vaccinated group but with limited evidence of an enhanced control of viraemia. Analysis of the lungs during the resolution of infection showed significant M/NSP5 specific IFN-γ responses from CD8 rather than CD4 T cells. Vaccine primed CD8 T cell responses may therefore be required for protection and future work should focus on enhancing the cross-presentation of M/NSP5 to CD8 T cells.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vacunas Virales / Linfocitos T / Síndrome Respiratorio y de la Reproducción Porcina / Antígenos Virales Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Vet Microbiol Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vacunas Virales / Linfocitos T / Síndrome Respiratorio y de la Reproducción Porcina / Antígenos Virales Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Vet Microbiol Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Países Bajos