Adenovirus vectors
View Patent ↗An adenoviral vector comprising a promoter further comprising a fragment of the 5′ untranslated region of the CMV IE1 gene including intron A and a nucleic acid sequence encoding a pathogen or tumor antigen for use as a medicament.
1. A recombinant adenoviral vector comprising a promoter and at least one nucleic acid sequence encoding an antigen of a bacterial pathogen or a parasitic pathogen under the control of said promoter, wherein said promoter consists of SEQ ID NO: 7 and wherein said parasitic antigen is not a murine malaria parasite antigen.
2. The adenoviral vector of claim 1 , wherein said vector is replication deficient.
3. The adenoviral vector of claim 1 , wherein the adenoviral vector is the chimpanzee adenoviral vector AdC6 (C6), AdC7 (C7), or AdC9 (C9) vector.
4. The adenoviral vector of claim 1 , wherein the promoter excludes exon B of the cytomegalovirus immediate early 1 (CMV IE1) gene.
5. The adenoviral vector of claim 1 , wherein the parasitic antigen is a malaria antigen, which is not a murine malaria antigen.
6. The adenoviral vector of claim 5 , wherein the malaria antigen is a Plasmodium falciparum antigen.
7. The adenoviral vector of claim 5 , wherein the malaria antigen is a pre-erythrocytic malaria antigen or a blood stage malaria antigen.
8. The adenoviral vector of claim 6 , wherein the malaria antigen is selected from the group consisting of multi-epitope string-thrombospondin-related adhesion protein (ME-TRAP), circumsporozoite protein (CSP), and merozoite surface protein-1 (MSP-1).
9. The adenoviral vector of claim 8 , wherein the MSP-1 malaria antigen is PfM117 having the amino acid sequence of SEQ ID NO: 1, or PfM128 having the amino acid sequence of SEQ ID NO: 3.
10. The adenoviral vector of claim 1 , wherein the bacterial antigen is the Mycobacterium tuberculosis antigen 85A.
11. An immunogenic composition comprising the adenoviral vector of claim 1 admixed with one or more pharmaceutically acceptable vehicles, carriers, diluents, or adjuvants.
12. A composition or a kit comprising:
(a) a priming composition comprising the adenoviral vector of claim 1 and
(b) a boosting composition comprising a recombinant pox virus vector, said pox virus vector further comprising at least one nucleic acid sequence encoding an antigen from a bacterial pathogen or a parasitic pathogen which antigen is the same as the antigen in the priming composition.
13. The composition or the kit of claim 12 , wherein the promoter excludes exon B of the CMV IE1 gene.
14. The composition or the kit of claim 12 , wherein the parasitic antigen is a malaria antigen, which is not a murine malaria antigen.
15. The composition or the kit of claim 14 , wherein the malaria antigen is a Plasmodium falciparum antigen.
16. The composition or the kit of claim 14 , wherein the malaria antigen is selected from the group consisting of multi-epitope string-thrombospondin-related adhesion protein (ME-TRAP), circumsporozoite protein (CSP), and merozoite surface protein-1 (MSP-1).
17. The composition or the kit of claim 16 , wherein the MSP-1 malaria antigen is PfM117 having the amino acid sequence of SEQ ID NO: 1, or PfM128 having the amino acid sequence of SEQ ID NO: 3.
18. A composition comprising the immunogenic composition of claim 11 and a CpG adjuvant.
19. A method of eliciting an immune response to an antigen of a bacterial pathogen or a parasitic pathogen in a mammalian subject comprising administering to the subject an effective amount of the immunogenic composition of claim 11 sufficient to elicit the immune response to the antigen in said subject.
20. A method of enhancing T cell immune responses to the immunogenic composition of claim 11 in a mammalian subject comprising administering said immunogenic composition in combination with a CpG adjuvant to said mammalian subject.