Polynucleotides encoding antigenic HIV type B polypeptides, polypeptides and uses thereof
The present invention relates to polynucleotides encoding immunogenic HIV polypeptides. Uses of the polynucleotides in applications including immunization, generation of packaging cell lines, and production of HIV polypeptides are also described. Polynucleotides encoding antigenic HIV polypeptides are described, as are uses of these polynucleotides and polypeptide products therefrom, including formulations of immunogenic compositions and uses thereof.
1. An expression cassette, comprising a polynucleotide sequence encoding a polypeptide including an HIV Tat polypeptide, wherein the polynucleotide sequence encoding said Tat polypeptide comprises a sequence having at least 90% sequence identity to the full length of sequence SEQ ID NO:52.
2. A recombinant expression system for use in a selected host cell, comprising, an expression cassette of claim 1 , and wherein said polynucleotide sequence is operably linked to control elements compatible with expression in the selected host cell.
3. The recombinant expression system of claim 2 , wherein said control elements are selected from the group consisting of a transcription promoter, a transcription enhancer element, a transcription termination signal, polyadenylation sequences, sequences for optimization of initiation of translation, and translation termination sequences.
4. The recombinant expression system of claim 2 , wherein said transcription promoter is selected from the group consisting of CMV, CMV+intron A, SV40, RSV, HIV-Ltr, MMLV-ltr, and metallothionein.
5. An isolated cell comprising an expression cassette of claim 1 , and wherein said polynucleotide sequence is operably linked to control elements compatible with expression in the selected cell.
6. The cell of claim 5 , wherein the cell is a mammalian cell.
7. The cell of claim 6 , wherein the cell is selected from the group consisting of BHK, VERO, HT1080, 293, RD, COS-7, and CHO cells.
8. The cell of claim 7 , wherein said cell is a CHO cell.
9. The cell of claim 5 , wherein the cell is an insect cell.
10. The cell of claim 9 , wherein the cell is either Trichoplusia ni (Tn5) or Sf9 insect cells.
11. The cell of claim 5 , wherein the cell is a bacterial cell.
12. The cell of claim 5 , wherein the cell is a yeast cell.
13. The cell of claim 5 , wherein the cell is a plant cell.
14. The cell of claim 5 , wherein the cell is an antigen presenting cell.
15. The cell of claim 14 , wherein the antigen presenting cell is a lymphoid cell selected from the group consisting of macrophages, monocytes, dendritic cells, B-cells, T-cells, stem cells, and progenitor cells thereof.
16. The cell of claim 5 , wherein the cell is a primary cell.
17. The cell of claim 5 , wherein the cell is an immortalized cell.
18. The cell of claim 5 , wherein the cell is a tumor-derived cell.
19. A vector for use in generating an immune response in a mammalian subject, comprising
an expression cassette of claim 1 , and wherein said polynucleotide sequence is operably linked to control elements compatible with expression of the polynucleotide in the subject.
20. A method of DNA immunization of a subject, comprising,
introducing a vector of claim 19 into said subject under conditions that are compatible with expression of said expression cassette in said subject.
21. The method of claim 20 , wherein said vector is a nonviral vector.
22. The method of claim 20 , wherein said vector is delivered using a particulate carrier.
23. The method of claim 22 , wherein said vector is coated on a gold or tungsten particle and said coated particle is delivered to said subject using a gene gun.
24. The method of claim 20 , wherein said vector is encapsulated in a liposome preparation.
25. The method of claim 20 , wherein said vector is a viral vector.
26. The method of claim 25 , wherein said viral vector is a retroviral vector.
27. The method of claim 25 , wherein said viral vector is an alphaviral vector.
28. The method of claim 25 , wherein said viral vector is a lentiviral vector.
29. The method of claim 20 , wherein said subject is a mammal.
30. The method of claim 29 , wherein said mammal is a human.
31. A method of generating an immune response in a subject, comprising
transfecting cells of said subject with a vector of claim 19 , under conditions that permit the expression of said polynucleotide and production of said polypeptide, thereby eliciting an immunological response to said polypeptide.
32. The method of claim 31 , wherein said vector is a nonviral vector.
33. The method of claim 31 , wherein said vector is delivered using a particulate carrier.
34. The method of claim 33 , wherein said vector is coated on a gold or tungsten particle and said coated particle is delivered to said vertebrate cell using a gene gun.
35. The method of claim 31 , wherein said vector is encapsulated in a liposome preparation.
36. The method of claim 31 , wherein said vector is a viral vector.
37. The method of claim 36 , wherein said viral vector is a retroviral vector.
38. The method of claim 36 , wherein said viral vector is an alphaviral vector.
39. The method of claim 36 , wherein said viral vector is a lentiviral vector.
40. The method of claim 31 , wherein said subject is a mammal.
41. The method of claim 40 , wherein said mammal is a human.
42. The method of claim 31 , wherein said transfecting is done ex vivo and said transfected cells are reintroduced into said subject.
43. The method of claim 31 , wherein said transfecting is done in vivo in said subject.
44. The method of claim 31 , where said immune response is a humoral immune response.
45. The method of claim 31 , where said immune response is a cellular immune response.
46. The method of claim 31 , wherein the vector is administered intramuscularly, intramucosally, intranasally, subcutaneously, intradermally, transdermally, intravaginally, intrarectally, orally or intravenously.