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A bivalent B-cell epitope dendrimer peptide can confer long-lasting immunity in swine against foot-and-mouth disease.
Cañas-Arranz, Rodrigo; Forner, Mar; Defaus, Sira; Rodríguez-Pulido, Miguel; de León, Patricia; Torres, Elisa; Bustos, María J; Borrego, Belén; Sáiz, Margarita; Blanco, Esther; Andreu, David; Sobrino, Francisco.
Afiliação
  • Cañas-Arranz R; Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Madrid, Spain.
  • Forner M; Departament de Ciències, Experimentals i de la Salut, Universitat Pompeu-Fabra, Barcelona, Spain.
  • Defaus S; Departament de Ciències, Experimentals i de la Salut, Universitat Pompeu-Fabra, Barcelona, Spain.
  • Rodríguez-Pulido M; Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Madrid, Spain.
  • de León P; Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Madrid, Spain.
  • Torres E; Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Madrid, Spain.
  • Bustos MJ; Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Madrid, Spain.
  • Borrego B; Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Spain.
  • Sáiz M; Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Madrid, Spain.
  • Blanco E; Centro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Spain.
  • Andreu D; Departament de Ciències, Experimentals i de la Salut, Universitat Pompeu-Fabra, Barcelona, Spain.
  • Sobrino F; Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Madrid, Spain.
Transbound Emerg Dis ; 67(4): 1614-1622, 2020 Jul.
Article em En | MEDLINE | ID: mdl-31994334
Foot-and-mouth disease virus (FMDV) causes a widely extended contagious disease of livestock. We have previously reported that a synthetic dendrimeric peptide, termed B2 T(mal), consisting of two copies of a B-cell epitope [VP1(140-158)] linked through maleimide groups to a T-cell epitope [3A(21-35)] of FMDV, elicits potent B- and T-cell-specific responses and confers solid protection in pigs to type O FMDV challenge. Longer duration of the protective response and the possibility of inducing protection after a single dose are important requirements for an efficient FMD vaccine. Herein, we show that administration of two doses of B2 T(mal) elicited high levels of specific total IgGs and neutralizing antibodies that lasted 4-5 months after the peptide boost. Additionally, concomitant levels of IFN-γ-producing specific T cells were observed. Immunization with two doses of B2 T(mal) conferred a long-lasting reduced susceptibility to FMDV infection, up to 136 days (19/20 weeks) post-boost. Remarkably, a similar duration of the protective response was achieved by a single dose of B2 T(mal). The effect on the B2 T(mal) vaccine of RNA transcripts derived from non-coding regions in the FMDV genome, known to enhance the immune response and protection induced by a conventional inactivated vaccine, was also analysed. The contribution of our results to the development of FMD dendrimeric vaccines is discussed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Doenças dos Suínos / Vacinas Virais / Epitopos de Linfócito B / Vírus da Febre Aftosa / Febre Aftosa Limite: Animals Idioma: En Revista: Transbound Emerg Dis Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Doenças dos Suínos / Vacinas Virais / Epitopos de Linfócito B / Vírus da Febre Aftosa / Febre Aftosa Limite: Animals Idioma: En Revista: Transbound Emerg Dis Ano de publicação: 2020 Tipo de documento: Article