Molecular adjuvant and vaccine
The invention relates to the fields of vaccines and vaccine adjuvants, and generally relates to polynucleotide adjuvants, polynucleotide vaccines and vaccine compositions. More specifically, the invention relates to said polynucleotides and vaccine compositions for use in inducing or enhancing a prophylactic or therapeutic immune response in a mammalian subject. Furthermore, it relates to said polynucleotides and vaccine compositions for use in the prophylactic or therapeutic treatment of an infectious disease, such as in the prophylactic or therapeutic treatment of leishmaniasis.
1. A method for protecting a canine or human subject from leishmaniasis, the method comprising administering to the subject a plasmid comprising the nucleic acid sequence of SEQ ID NO: 3 and the nucleic acid sequence of SEQ ID NO: 5.
2. The method of claim 1 , wherein said nucleic acid sequence SEQ ID NO: 3 and said nucleic acid sequence of SEQ ID NO: 5 are operably linked to a control sequence.
3. The method of claim 1 , wherein said plasmid is a circular or linear bacterial DNA.
4. The method of claim 1 , wherein the plasmid comprises no antibiotic resistance genes.
5. The method of claim 1 , wherein the plasmid is the pPAL-LACK plasmid of SEQ ID NO: 23.
6. A vaccine for protecting a canine or human subject from leishmaniasis, the vaccine comprising a pharmaceutically acceptable carrier, additive or excipient and a plasmid the nucleic acid sequence of SEQ ID NO: 3, and the nucleic acid sequence of SEQ ID NO:5.
7. The method of claim 1 , wherein said subject is a canine and wherein said leishmaniasis is canine leishmaniasis.
8. The method of claim 1 , wherein the administering comprises a homologous prime-boost regime.
9. A method for producing antibodies, comprising immunizing a canine or human subject with a polynucleotide sequence comprising the nucleic acid of SEQ ID NO: 3 and the nucleic acid of SEQ ID NO: 5, or a pharmaceutical composition comprising the same.
10. The vaccine of claim 6 , wherein the plasmid is the pPAL-LACK plasmid of SEQ ID NO: 23.
11. The method of claim 9 , wherein the plasmid is the pPAL-LACK plasmid of SEQ ID NO: 23.
12. The method of claim 1 , wherein said subject is a human subject.
13. The method of claim 12 , wherein said leishmaniasis is visceral leishmaniasis.