TY - JOUR
T1 - A bivalent B-cell epitope dendrimer peptide can confer long-lasting immunity in swine against foot-and-mouth disease
AU - Cañas-Arranz, Rodrigo
AU - Forner, Mar
AU - Defaus, Sira
AU - Rodríguez-Pulido, Miguel
AU - de León, Patricia
AU - Torres, Elisa
AU - Bustos, María J.
AU - Borrego, Belén
AU - Sáiz, Margarita
AU - Blanco, Esther
AU - Andreu, David
AU - Sobrino, Francisco
N1 - Publisher Copyright:
© 2020 Blackwell Verlag GmbH
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Foot-and-mouth disease virus (FMDV) causes a widely extended contagious disease of livestock. We have previously reported that a synthetic dendrimeric peptide, termed B2T(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 B2T(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 B2T(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 B2T(mal). The effect on the B2T(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.
AB - Foot-and-mouth disease virus (FMDV) causes a widely extended contagious disease of livestock. We have previously reported that a synthetic dendrimeric peptide, termed B2T(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 B2T(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 B2T(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 B2T(mal). The effect on the B2T(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.
KW - dendrimer peptide
KW - FMDV
KW - protection
KW - swine
KW - vaccine
UR - https://www.scopus.com/pages/publications/85079384964
U2 - 10.1111/tbed.13497
DO - 10.1111/tbed.13497
M3 - Article
C2 - 31994334
AN - SCOPUS:85079384964
SN - 1865-1674
VL - 67
SP - 1614
EP - 1622
JO - Transboundary and emerging diseases
JF - Transboundary and emerging diseases
IS - 4
ER -