2018
DOI: 10.1016/j.vaccine.2018.02.074
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A canine adenovirus type 2 vaccine vector confers protection against foot-and-mouth disease in guinea pigs

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Cited by 12 publications
(14 citation statements)
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“…For instance, RDAd vaccine expressing only the FMDV VP1 capsid protein can only induce low levels of neutralizing antibodies [61], whereas RDAd vaccines expressing the complete P1-encoded capsid polypeptide of FMDV and the 3C pro protease can fully protect swine and cattle [58,62,63]. Protection was also achieved in animal models with this FMDV antigen formulation expressed in an RDCaAd2 vector instead of the "traditional" RDHuAd5 vector [56], highlighting the efficacy of this antigen construct. The choice of antigen for vaccination should, therefore, be based on the knowledge of host-pathogen interactions and the characterization of the protective immunity that arises during infection.…”
Section: Antigen-encoding Rdad As Vaccinesmentioning
confidence: 98%
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“…For instance, RDAd vaccine expressing only the FMDV VP1 capsid protein can only induce low levels of neutralizing antibodies [61], whereas RDAd vaccines expressing the complete P1-encoded capsid polypeptide of FMDV and the 3C pro protease can fully protect swine and cattle [58,62,63]. Protection was also achieved in animal models with this FMDV antigen formulation expressed in an RDCaAd2 vector instead of the "traditional" RDHuAd5 vector [56], highlighting the efficacy of this antigen construct. The choice of antigen for vaccination should, therefore, be based on the knowledge of host-pathogen interactions and the characterization of the protective immunity that arises during infection.…”
Section: Antigen-encoding Rdad As Vaccinesmentioning
confidence: 98%
“…One of the main barriers for the development of nonhuman RDAd vectors is the necessity to construct cell lines capable of complementing the viral genome so that these vaccines can be propagated. The production of RD vectors has nonetheless been achieved for several nonprimate species [48,53], and RDCaAd2 vectors expressing immunogenic viral subunits have shown potential for vaccination against rabies [54], bluetongue virus (BTV) [55], or FMDV [56]. Because Ad infect a wide range of mammalian cells from different species, these nonhuman RDAd vectors could also be used to circumvent pre-existing immunity.…”
Section: Human Vs Nonhuman Adenovirus For Veterinary Usementioning
confidence: 99%
“…All the HPV L1 reference sequences of 6,16,18,31,33,34,35,45,52, and 58 were obtained from the PaVE website (http://pave.niaid.nih.gov) (GenBank accession number GI:60955, GI:333031, GI:60975, GI:333048, GI:333049, GI:9627334, GI:396997, GI:397022, GI:397038, and GI:222386, respectively). It was previously shown that a human codon optimized L1 gene resulted in higher accumulation of L1 when expressed in plants compared to expression of plant codon optimized and native L1 gene sequences [23].…”
Section: Hpv Recombinant Plasmidsmentioning
confidence: 99%
“…The plant-produced VLP vaccine candidates and empty vector negative control were emulsified in mineral oil MONTANIDE™ ISA 50 V2 adjuvant at a 60:40 (vaccine:adjuvant) ratio. MONTANIDE ISA 50 V2 is a ready-to-use oily vaccine adjuvant that has previously been used in mice [33,34]. Purified plant-produced HPV L1 proteins were used as coating antigens in ELISAs.…”
Section: Immunization Of Micementioning
confidence: 99%
“…Foot-and-mouth disease (FMD) is one of the most important infectious diseases of cloven-hoofed livestock and wildlife [1] , which is an acute, hot, and highly contagious infectious disease caused by the foot-and-mouth disease virus (FMDV). In 2007, the British FMD epidemic caused a major blow to the export of cloven-hoofed animals and their products (http :// www.…”
Section: Introductionmentioning
confidence: 99%