H5 proteins, nucleic acid molecules and vectors encoding for those, and their medicinal use
The present invention relates to novel hemagglutinin H5 proteins, nucleic acids and vectors encoding for those as well as vaccines comprising any of such H5 proteins, nucleic acids or vectors encoding for those H5 proteins. Moreover, the present invention also relates to the medicinal use of any of such compositions in humans and animals.
1. A vaccine comprising
a. one or more immunogenic components selected from the group consisting of
i. an isolated nucleic acid encoding a recombinant H5 protein, wherein the recombinant H5 protein comprises SEQ ID NO: 4 and includes amino acid 223N, modification 328K+, and amino acid 94N, wherein numbering of the amino acid positions refers to the amino acid position as exemplified by SEQ ID NO: 1 and wherein the modification 328K+ means that a second lysine (K+) is inserted at amino acid position 328 of the H5 protein,
ii. a vector comprising the isolated nucleic acid,
iii. the recombinant H5 protein, and
iv. any combination thereof; and
b. a pharmaceutical acceptable carrier and/or excipient.
2. The vaccine of claim 1 , wherein the excipient is one or more adjuvants.
3. The vaccine of claim 2 , wherein the adjuvant is an EMULSIGEN® oil-in-water emulsion-based adjuvant.
4. The vaccine of claim 1 , wherein the vaccine further comprises one or more additional antigens.
5. The vaccine of claim 4 , wherein the additional antigen is an antigen of a poultry pathogen or a mammalian pathogen.
6. The vaccine of claim 4 , wherein the additional antigen is a H3, H7, or H9 protein of an influenza virus.
7. The vaccine of claim 1 , wherein the vector is a recombinant baculovirus.
8. The vaccine of claim 1 , wherein an immunogenic component is the isolated nucleic acid.
9. The vaccine of claim 1 , wherein an immunogenic component is the vector.
10. The vaccine of claim 1 , wherein an immunogenic component is the recombinant H5 protein.
11. The vaccine of claim 1 , wherein an immunogenic component is a combination.
12. A method of making a vaccine comprising:
a. obtaining one or more immunogenic components selected from the group consisting of
i. an isolated nucleic acid encoding a recombinant H5 protein, wherein the recombinant H5 protein comprises SEQ ID NO: 4 and includes amino acid 223N, modification 328K+, and amino acid 94N, wherein numbering of the amino acid positions refers to the amino acid position as exemplified by SEQ ID NO: 1 and wherein the modification 328K+ means that a second lysine (K+) is inserted at amino acid position 328 of the H5 protein,
ii. a vector comprising the isolated nucleic acid,
iii. the recombinant H5 protein, and
iv. any combination thereof; and
b. admixing one or more immunogenic components with a pharmaceutical acceptable carrier and/or excipient.
13. The method of claim 12 , wherein the excipient is one or more adjuvants.
14. The method of claim 13 , wherein the adjuvant is an EMULSIGEN® oil-in-water emulsion-based adjuvant.
15. The method of claim 12 , further comprising admixing one or more additional antigens into the vaccine.
16. The method of claim 15 , wherein an additional antigen is an antigen of a poultry pathogen or a mammalian pathogen.
17. The method of claim 15 , wherein an additional antigen is a H3, H7, or H9 protein of an influenza virus.