Vaccine in the form of a recombinant sero type 9 avian adenovirus vector
AssigneeGrupo Industrial Pecuario, S.A. De C.V.
InventorsBernardo Lozano-Dubernard, Ernesto Soto-Priante, David Sarfati-Mizrahi
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AssigneeGrupo Industrial Pecuario, S.A. De C.V.
InventorsBernardo Lozano-Dubernard, Ernesto Soto-Priante, David Sarfati-Mizrahi
Estimating the term…
A recombinant vaccine comprising a serotype 9 fowl adenovirus vector (FAdV-9) having at least one exogenous nucleotide sequence inserted encoding at least one antigen of a disease of interest and replacing the adenovirus genome non-essential region, and a pharmaceutically acceptable vehicle, adjuvant and/or excipient, wherein the at least one exogenous nucleotide sequence encoding at least one antigen of a disease of interest and replacing the adenovirus genome non-essential region is located between the 491 and 2782 nucleotides. The vector of this vaccine is stable for industrial scale production. When administering this vaccine in combination with a vaccine against Marek's disease, both vaccines produce an adequate immune response which is not affected by interference between each other. In the same way, effectiveness of the recombinant vaccine is not affected by maternal antibodies, and is capable of inducing both an early and lasting protective response, even with only one application.
A recombinant vaccine comprising a serotype 9 fowl adenovirus vector (FAdV-9) having at least one exogenous nucleotide sequence inserted encoding at least one antigen of a disease of interest and replacing the adenovirus genome non-essential region, and a pharmaceutically acceptable vehicle, adjuvant and/or excipient, wherein the FAdV-9 vector is live, and the exogenous nucleotide sequence is located between the 491 and 2782 nucleotides, and wherein the recombinant vaccine provides protection, with one dose, up to at least 90 days after its administration.
A master seed of a serotype-9 fowl adenovirus recombinant virus (FAdV-9) which has an exogenous nucleotide sequence inserted encoding a disease of interest antigen and replacing the adenovirus genome non-essential region, located between the 491 and 2782 nucleotides, wherein it is obtained after 6 to 11 passes in cell culture.
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