IP Library Granted Patent US 7,211,659
Granted Patent B2
US 7,211,659 · App. 10/190,435 · Granted May 1, 2007

Polynucleotides encoding antigenic HIV type C polypeptides, polypeptides and uses thereof

Assignee: Chiron Corporation
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Quick Facts
Patent No.
US 7,211,659
App. No.
10/190,435
Granted
May 1, 2007
Kind
B2
Abstract

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.

Claims (49)

1. An expression cassette, comprising a polynucleotide sequence encoding a polypeptide including an immunogenic HIV Gag polypeptide, wherein the polynucleotide sequence encoding said immunogenic HIV Gag polypeptide comprises a sequence having at least 90% sequence identity to SEQ ID NO:9.

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, HJV-Ltr, MMLV-ltr, and metallothionein.

5. A 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 method for producing a polypeptide including HIV Gag polypeptide sequences, said method comprising,

incubating the cells of claim 5 , under conditions for producing said polypeptide.

20. A vector for use in a mammalian subject, wherein the vector comprises an expression cassette of claim 1 , and wherein said polynucleotide sequence is operably linked to control elements compatible with expression in the subject.

21. A method of DNA immunization of a subject, comprising,

introducing a vector of claim 20 into said subject under conditions that are compatible with expression of said expression cassette in said subject.

22. The method of claim 21 , wherein said vector is a nonviral vector.

23. The method of claim 21 , wherein said vector is delivered using a particulate carrier.

24. The method of claim 23 , wherein said vector is coated on a gold or tungsten particle and said coated particle is delivered to said subject using a gene gun.

25. The method of claim 21 , wherein said vector is encapsulated in a liposome preparation.

26. The method of claim 21 , wherein said vector is a viral vector.

27. The method of claim 26 , wherein said viral vector is a retroviral vector.

28. The method of claim 26 , wherein said viral vector is an alphaviral vector.

29. The method of claim 26 , wherein said viral vector is a lentiviral vector.

30. The method of claim 21 , wherein said subject is a mammal.

31. The method of claim 30 , wherein said mammal is a human.

32. A method of generating an immune response in a subject, comprising transfecting cells of said subject with a vector of claim 20 , under conditions that permit the expression of said polynucleotide and production of said polypeptide, thereby eliciting an immunological response to said polypeptide.

33. The method of claim 32 , wherein said vector is a nonviral vector.

34. The method of claim 32 , wherein said vector is delivered using a particulate carrier.

35. The method of claim 32 , 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.

36. The method of claim 32 , wherein said vector is encapsulated in a liposome preparation.

37. The method of claim 32 , wherein said vector is a viral vector.

38. The method of claim 37 , wherein said viral vector is a retroviral vector.

39. The method of claim 37 , wherein said viral vector is an alphaviral vector.

40. The method of claim 37 , wherein said viral vector is a lentiviral vector.

41. The method of claim 32 , wherein said subject is a mammal.

42. The method of claim 41 , wherein said mammal is a human.

43. The method of claim 32 , wherein said transfecting is done ex vivo and said transfected cells are reintroduced into said subject.

44. The method of claim 32 , wherein said transfecting is done in vivo in said subject.

45. The method of claim 32 , where said immune response is a humoral immune response.

46. The method of claim 32 , where said immune response is a cellular immune response.

47. The method of claim 32 , wherein the vector is administered intramuscularly, intramucosally, intranasally, subcutaneously, intradermally, transdermally, intravaginally, intrarectally, orally or intravenously.

Assignments (4)
MERGER AND CHANGE OF NAME Recorded Jul 22, 2015
From: NOVARTIS BIOTECH PARTNERSHIP, INC.; CHIRON CORPORATION
To: NOVARTIS VACCINES AND DIAGNOSTICS, INC.
Reel/Frame 036157/0559 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 7, 2010
From: CHIRON CORPORATION
To: NOVARTIS VACCINES & DIAGNOSTICS, INC.
Reel/Frame 025462/0947 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2004
From: ENGELBRECHT, SUSAN; VAN RENSBURG, ESTRALITA JANSE; SCRIBA, THOMAS JENS
To: STELLENBOSCH, UNIVERSITY OF
Reel/Frame 014347/0478 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2004
From: ZUR MEGEDE, JAN; BARNETT, SUSAN W.; LIANG, YING
To: CHIRON CORPORATION
Reel/Frame 014928/0264 →
Continuity (4)
Provisional Application 6034987100 · Jan 16, 2002
Provisional Application 6031686000 · Aug 31, 2001
Provisional Application 6030319200 · Jul 5, 2001
Related Publication 20030143248A1 · Jul 31, 2003