B7-DC variants

• US 8,039,589 B1
• Filed: 10/31/2007
• Issued: 10/18/2011
• Est. Priority Date: 10/04/2002
• Status: Active Grant

• Current Assignee: Mayo Foundation For Medical Education And Research (Mayo Clinic)
• Original Assignee: Mayo Foundation For Medical Education And Research (Mayo Clinic)
• Inventors: Chen, Lieping
• Primary Examiner(s): OUSPENSKI, ILIA I
• Application Number:
  US11/932,471
• Time in Patent Office: 1,448 Days
• Field of Search: None
• US Class Current: 530/350
• CPC Class Codes: A61P 37/04 Immunostimulants
• CPC Class Codes: C07K 14/47 from mammals
• CPC Class Codes: C07K 14/70532 B7 molecules, e.g. CD80, CD86

Abstract

Variant costimulatory polypeptides, nucleic acids encoding such polypeptides, and methods for using the polypeptides and nucleic acids to enhance a T cell response are provided herein.

Claims

1. An isolated variant B7-DC polypeptide comprising an IgV domain, wherein the variant polypeptide is a variant of wild-type B7-DC polypeptide, has altered binding affinity for PD-1 compared to the wild-type B7-DC polypeptide, and comprises a substitution of an amino acid in the A′

, B, C, C′

, C″

, D, E, F, or G β

-strand of wild-type B7-DC polypeptide according to SEQ ID NO;

5 or 6.

2. The isolated variant polypeptide of claim 1, which is a variant of murine B7-DC.

3. The isolated variant polypeptide of claim 1, comprising a substitution of the amino acid at position 111 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

4. The isolated variant polypeptide of claim 3, wherein said substitution comprises replacing the amino acid at position 111 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a serine residue.

5. The isolated variant polypeptide of claim 1 comprising a substitution of the amino acid at position 113 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

6. The isolated variant polypeptide of claim 5, wherein said substitution comprises replacing the amino acid at position 113 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a serine residue.

7. The isolated variant polypeptide of claim 1 comprising a substitution of the amino acid at position 56 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

8. The isolated variant polypeptide of claim 7, wherein said substitution comprises replacing the amino acid at position 56 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a serine residue.

9. The isolated variant polypeptide of claim 1, comprising a substitution of the amino acid at position 67 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

10. The isolated variant polypeptide of claim 9, wherein said substitution comprises replacing the amino acid at position 67 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a tyrosine residue.

11. The isolated variant polypeptide of claim 1, comprising a substitution of the amino acid at position 71 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

12. The isolated variant polypeptide of claim 11, wherein said substitution comprises replacing the amino acid at position 71 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a serine residue.

13. The isolated variant polypeptide of claim 1 comprising a substitution of the amino acid at position 101 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

14. The isolated variant polypeptide of claim 13, wherein said substitution comprises replacing the amino acid at position 101 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a serine residue.

15. The isolated variant polypeptide of claim 1 comprising a substitution of the amino acid at position 105 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

16. The isolated variant polypeptide of claim 15, wherein said substitution comprises replacing the amino acid at position 105 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with an alanine residue.

17. The variant B7-DC polypeptide or fragment thereof of claim 1, wherein the variant B7-DC polypeptide or fragment thereof has decreased binding affinity for PD-1 compared to wild-type B7-DC polypeptide.

18. A fusion polypeptide comprising a first fusion partner comprising the polypeptide of claim 17, and a second fusion partner.

19. The fusion polypeptide of claim 18, wherein the second fusion partner comprises one or more domains of an Ig heavy chain constant region.

20. A method for enhancing an immune response in a mammal comprising administering to the mammal the isolated polypeptide of claim 1 or claim 19, or a nucleic acid molecule encoding the polypeptide.

21. The method of claim 20, wherein the mammal is a human.

29. The isolated polypeptide of claim 1, wherein the B7-DC polypeptide is human B7-DC.

30. The fusion polypeptide of claim 19, wherein the second polypeptide comprises an amino acid sequence corresponding to the hinge, C_H2 and C_H3 regions of a human immunoglobulin chain.

31. The fusion polypeptide of claim 30, wherein the first polypeptide comprises the extracellular domain of B7-DC or a fragment thereof, and wherein the second polypeptide comprises an amino acid sequence corresponding to the hinge, C_H2 and C_H3 regions of a human immunoglobulin chain.

32. The isolated variant B7-DC polypeptide of claim 17, wherein the variant B7-DC polypeptide or fragment thereof enhances an immune response in a mammal.

33. The isolated variant B7-DC polypeptide or fragment thereof of claim 1, wherein the variant B7-DC polypeptide or fragment thereof has increased binding affinity for PD-1 compared to wild-type B7-DC polypeptide.

34. The isolated variant B7-DC polypeptide of claim 33, wherein the variant B7-DC polypeptide or fragment thereof enhances an immune response in a mammal.

35. The isolated variant polypeptide of claim 33, which is a variant of murine or human B7-DC.

36. The isolated variant polypeptide of claim 33, comprising a substitution of the amino acid at position 58 number from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

37. The isolated variant polypeptide of claim 36, wherein the substitution comprises replacing the amino acid at position 58 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a tyrosine residue.

38. An isolated fusion polypeptide comprising a first fusion partner comprising the polypeptide of claim 33, and a second fusion partner.

39. The fusion polypeptide of claim 38, wherein the second fusion partner comprises one or more domains of an Ig heavy chain constant region.

40. The fusion polypeptide of claim 38, wherein the second polypeptide comprises an amino acid sequence corresponding to the hinge, C_H2 and C_H3 regions of a human immunoglobulin chain.

41. The fusion polypeptide of claim 38, wherein the first polypeptide comprises the extracellular domain of B7-DC or a fragment thereof, and wherein the second polypeptide comprises an amino acid sequence corresponding to the hinge, C_H2 and C_H3 regions of a human immunoglobulin chain.

22. An isolated polypeptide fragment of murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5), the polypeptide fragment comprising amino acids 67-71, amino acids 101-105, or amino acids 111-113 of SEQ ID NO;

6, wherein the polypeptide inhibits binding of endogenous B7-DC to PD-1.

23. The fragment of claim 22, comprising amino acids 101-113 of murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

24. A method of inhibiting the interaction between PD-1 and B7-DC, the method comprising contacting a PD-1 polypeptide with the polypeptide fragment of claim 22.

25. The method of claim 24, wherein the PD-1 is in vitro.

26. The method of claim 24, wherein the PD-1 is in a mammal.

27. The method of claim 24, wherein the method comprises administering the polypeptide fragment to the mammal.

28. The method of claim 26, wherein the mammal is a human.

42. A fusion polypeptide comprising the IgV domain of B7-DC fused to a second polypeptide, wherein the IgV domain of B7-DC is from human (SEQ ID NO:

5) or murine B7-DC (SEQ ID NO;

6) and comprises an amino acid substitution relative to wildtype human (SEQ ID NO;

5) or murine (SEQ ID NO;

6) B7-DC IgV domain, wherein the substitution alters binding affinity for PD-1 compared to the wild-type B7-DC polypeptide.

43. The fusion polypeptide of claim 42, wherein the second polypeptide comprises an amino acid sequence corresponding to the hinge, C_H2 and C_H3 regions of a human immunoglobulin chain.

44. The fusion polypeptide of claim 42 wherein the amino acid substitution in the extracellular domain occurs at the amino acid residue corresponding to amino acid position 111 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

45. The fusion polypeptide of claim 44, wherein the amino acid substitution is with a serine residue.

46. The fusion polypeptide of claim 42, wherein the substitution is at the amino acid residue corresponding to position 113 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

47. The fusion polypeptide of claim 46, wherein the substitution is with a serine residue.

48. The fusion polypeptide of claim 42 comprising a substitution of the amino acid is at the amino acid residue corresponding to position 56 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

49. The fusion polypeptide of claim 48, wherein the substitution comprises replacing the amino acid corresponding the amino acid at position 56 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a serine residue.

50. The fusion polypeptide of claim 42, comprising a substitution of the amino acid corresponding to the amino acid at position 67 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

51. The fusion polypeptide of claim 50, wherein the substitution comprises replacing the amino acid corresponding to the amino acid at position 67 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a tyrosine.

52. The fusion polypeptide of claim 42, comprising a substitution of the amino acid corresponding to the amino acid at position 71 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

53. The fusion polypeptide of claim 52, wherein the substitution comprises replacing the amino acid corresponding to the amino acid at position 71 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a serine residue.

54. The fusion polypeptide of claim 42, comprising a substitution of the amino acid corresponding to the amino acid at position 101 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

55. The fusion polypeptide of claim 54, wherein the substitution comprises replacing the amino acid corresponding to the amino acid at position 101 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with a serine residue.

56. The fusion polypeptide of claim 42, comprising a substitution of the amino acid at position 105 corresponding to the amino acid numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5).

57. The fusion polypeptide of claim 56, wherein the substitution comprises replacing the amino acid corresponding to the amino acid at position 105 numbered from the initiation methionine of wild-type murine B7-DC (SEQ ID NO:

6) or human B7-DC (SEQ ID NO;

5) with an alanine.