Methods and compositions for producing an adenovirus vector for use with multiple vaccinations
Methods for generating immune responses using adenovirus vectors that allow multiple vaccinations with the same adenovirus vector and vaccinations in individuals with preexisting immunity to adenovirus are provided.
1. A composition comprising a replication defective adenovirus vector comprising 1) a deletion in the E2b region and 2) a nucleic acid sequence encoding an antigen, wherein the antigen is a viral protein, and wherein the viral protein is derived from an influenza virus.
2. The composition of claim 1 , wherein the replication defective adenovirus vector further comprises a deletion in the E1 region.
3. The composition of claim 1 , wherein the nucleic acid sequence encoding the antigen is located in the E1 region.
4. The composition of claim 1 , wherein the replication defective adenovirus vector further comprises a deletion in the E3 region.
5. The composition of claim 1 , wherein the nucleic acid sequence encoding the antigen is located in the E3 region.
6. The composition of claim 1 , wherein the replication defective adenovirus vector is derived from Adenovirus serotype 5.
7. The composition of claim 1 , wherein the composition comprises the replication defective adenovirus vector at a concentration of at least 10 10 virus particles/ml.
8. The composition of claim 1 , wherein the replication defective adenovirus vector is not helper-adenovirus dependent.
9. The composition of claim 1 , wherein the antigen is selected from the list consisting of influenza neuraminidase, hemagglutinin, and Matrix Protein M1.
10. The composition of claim 1 , wherein the influenza virus protein is derived from an influenza virus selected from the group consisting of: H5N1, H3N2, H9N1, H1N1, H2N2, H7N7, H1N2, H9N2, H7N2, H7N3, and H10N7.
11. The composition of claim 1 , further comprising an adjuvant.
12. The composition of claim 11 , wherein the adjuvant is granulocyte macrophage colony-stimulating factor (GM-CSF), granulocyte-colony stimulating factor (G-CSF), interferon-gamma (IFN-y), tumor necrosis factor-alpha (TNF-a), interleukin-2 (IL-2), IL-7, IL-12, IL-4, IL-5, IL-6, IL-10, IL-12, or a combination thereof.
13. The composition of claim 1 , wherein the composition is formulated for intramuscular, subcutaneous, or intradermal administration.
14. The composition of claim 1 , wherein the composition comprises the replication defective adenovirus vector at a concentration of at least 10 9 virus particles/ml.
15. The composition of claim 1 , wherein the antigen has been modified to increase immunogenicity.
16. The composition of claim 1 , further comprising a second replication defective adenovirus vector comprising a deletion in the E2b region and a nucleic acid sequence encoding an adjuvant.
17. A cell comprising the composition of claim 1 .
18. The cell of claim 16 , wherein the cell constitutively expresses DNA polymerase and preterminal protein.
19. The cell of claim 18 , wherein the cell is an antigen presenting cell.