METHODS AND COMPOSITIONS FOR MODULATING AN IMMUNE RESPONSE

• US 20140242077A1
• Filed: 01/23/2014
• Published: 08/28/2014
• Est. Priority Date: 01/23/2013
• Status: Abandoned Application

• Current Assignee: Abbvie Incorporated
• Original Assignee: Abbvie Incorporated
• Inventors: GHAYUR, Tariq, CHOI, Chee-Ho, TAO, Qingfeng, BARDWELL, Philip
• Application Number:
  US14/162,716
• Publication Number:
  US 20140242077A1
• Time in Patent Office: Days
• US Class Current: 424/136.1
• CPC Class Codes: A61K 2039/507 Comprising a combination of two or more separate antibodies
• CPC Class Codes: A61K 2039/572 cytotoxic response
• CPC Class Codes: A61K 39/3955 against proteinaceous materials, e.g. enzymes, hormones, lymphokines
• CPC Class Codes: C07K 16/2806 against CD2
• CPC Class Codes: C07K 16/2809 against the T-cell receptor (TcR)-CD3 complex
• CPC Class Codes: C07K 16/2863 against receptors for growth factors, growth regulators
• CPC Class Codes: C07K 16/2878 against the NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
• CPC Class Codes: C07K 16/2896 against molecules with a "CD"-designation, not provided for elsewhere
• CPC Class Codes: C07K 16/468 Immunoglobulins having two or more different antigen binding sites, e.g. multifunctional antibodies
• CPC Class Codes: C07K 2317/31 multispecific
• CPC Class Codes: C07K 2317/626 Diabody or triabody
• CPC Class Codes: C07K 2317/66 comprising a swap of domains, e.g. CH3-CH2, VH-CL or VL-CH1
• CPC Class Codes: C07K 2317/73 Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
• CPC Class Codes: C07K 2317/74 Inducing cell proliferation

Abstract

Provided are multispecific binding proteins and methods for using these multispecific binding proteins to modulate the activation state of immune cells, such as T-cells (e.g., cytotoxic T-cells). Also provided are methods of modulating an immune response (e.g., cell killing by cytotoxic T-cells) in a subject (e.g., a human subject). Also provided are nucleic acids, expression vectors and host cells encoding the multispecific binding proteins.

Claims

1. A multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, a second binding site that specifically binds to a cell surface receptor on an immune cell, and a third binding site that specifically binds to cell surface modulator on the immune cell.

2. The multispecific binding protein of claim 1, wherein the immune cell is a myeloid cell, a lymphoid cell;

an effector cell, a T-cell, a macrophage, a dendritic cell, a natural killer cell, an eosinophil, or a cytotoxic T-cell.

6. The multispecific binding protein of claim 1, wherein the cell surface receptor on the immune cell is a T-cell receptor (TCR) complex component.

7. The multispecific binding protein of claim 1, comprising a first binding site that specifically binds to a target cell antigen, a second binding site that specifically binds to a T-cell receptor (TCR) complex component on a T-cell, and a third binding site that specifically binds to a T-cell modulator on the T-cell.

8. The multispecific binding protein of claim 1, wherein the target cell antigen is a disease-associated antigen.

9. The multispecific binding protein of claim 1, wherein the target cell antigen is tumor-associated antigen.

11. The multispecific binding protein of claim 6, wherein the TCR complex component is CD3γ

, CD3δ

, or CD3ε

.

13. The multispecific binding protein of claim 1, wherein the modulator is a stimulator of T-cell activation.

14. The multispecific binding protein of claim 1, wherein the modulator is an inhibitor of T-cell activation.

18. The multispecific binding protein of claim 1 which is a DVD-Ig, half-DVD-Ig, a scDVD-Ig, an fDVD-Ig, an rDVD-Ig, a pDVD-Ig, an mDVD-Ig or a coDVD-Ig.

20. The method of claim 18, wherein the pDVD-Ig comprises first, second, third and fourth polypeptide chains,

wherein said first polypeptide chain comprises VD1-(X1)n-VD2-C-(X2)n, wherein VD1 is a first heavy chain variable domain, VD2 is a second heavy chain variable domain, C is a constant domain, X1 is a linker with the proviso that it is not a constant domain, and X2 is an Fc region;

wherein said second polypeptide chain comprises VD3-(X1)n-VD4-C-(X2)n, wherein VD3 is a first light chain variable domain, VD4 is a second light chain variable domain, C is a constant domain, X1 is a linker with the proviso that it is not a constant domain, and X2 does not comprise an Fc region;

wherein said third polypeptide chain comprises VD5-C-(X3)n, wherein VD5 is a third heavy chain variable domain, C is a constant domain, and X3 is an Fc region;

wherein said fourth polypeptide chain comprises VD6-C-(X3)n, wherein VD6 is a third light chain variable domain, C is a constant domain, and X4 does not comprise an Fc region;

wherein n is 0 or 1, and wherein the VD1 and VD3 domains on the first and second polypeptide chains form one functional binding site for a first antigen, the VD2 and VD4 domains on the first and second polypeptide chains form one functional binding site for a second antigen, and the VD5 and VD6 domains on the third and fourth polypeptide chains form one functional binding site for a third antigen.

21. The multispecific binding protein of claim 20, wherein the Fc region of the first and third polypeptide chains each comprises a mutation, wherein said mutations on the two Fc regions enhance heterodimerization of the first and third polypeptide chains.

22. The multispecific binding protein of claim 20, wherein the first antigen is the target cell antigen.

23. The multispecific binding protein of claim 20, wherein the second antigen is the TCR complex component.

24. The multispecific binding protein of claim 20, wherein the third antigen is the modulator.

25. The multispecific binding protein of claim 20, wherein VD1, VD2, or VD5 comprises a CDR region amino acid sequence selected from SEQ ID NO:

88-111.

28. The multispecific binding protein of claim 20, which comprises a polypeptide sequence selected from the group consisting of SEQ ID NO:

32-79.

46. A method of killing a target cell in a subject comprising administering to the subject an effective amount of the multispecific binding protein of claim 1 or therapeutic combination of claim 45, wherein the therapeutic combination comprises the first multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, and a second binding site that specifically binds to an immune cell receptor complex component on the immune cell;

and a second multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, and a second binding site that specifically binds to a cell surface modulator on the immune cell.

47. A method of killing a target cell in a subject comprising administering to the subject an effective amount of a multispecific binding protein of any one of claim 1, wherein the multispecific binding protein induces less cytokine production in the subject compared to administration of an equivalent effective amount of a therapeutic combination, wherein the therapeutic combination comprises a first multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, and a second binding site that specifically binds to an immune cell receptor complex component on the immune cell;

and a second multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, and a second binding site that specifically binds to a cell surface modulator on the immune cell.

48. A method of killing a target cell in a subject comprising administering to the subject an effective amount of a multispecific binding protein of claim 1, wherein the multispecific binding protein induces greater immune cell activation in the subject compared to administration of an equivalent effective amount of a therapeutic combination, wherein the therapeutic combination comprises a first multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, and a second binding site that specifically binds to an immune cell receptor complex component on the immune cell;

and a second multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, and a second binding site that specifically binds to a cell surface modulator on the immune cell.

74. A multispecific binding protein of claim 1, wherein the binding protein is a crystallized binding protein.

75. An isolated nucleic acid encoding the binding protein amino acid sequence of claim 1.

76. A vector comprising an isolated nucleic acid of claim 75.

77. A host cell comprising a vector of claim 76.

78. A method of producing a multispecific binding protein, comprising culturing the host cell described in claim 77 in culture medium under conditions sufficient to produce the binding protein.

79. A pharmaceutical composition comprising the binding protein of claim 1, and a pharmaceutically acceptable carrier.

80. A method of identifying a multispecific binding protein that modulates a T-cell response, the method comprising:

a) contacting a population of cytotoxic T-cells with a population of target cells in the presence and absence of the multispecific binding protein of claim 1, wherein the multispecific binding protein simultaneously and specifically binds to a cell surface co-stimulator or co-repressor on T-cells and to a cell surface antigen on a target cell; and

b) measuring the amount cell killing of the population of target cells, wherein an increase or decrease in cell killing in the presence of the multispecific binding, compared to the absence of the multispecific binding protein, identifies the multispecific binding protein as modulator of a T-cell response.

81. A method of identifying a multispecific binding protein that modulates a T-cell response, the method comprising:

a) contacting a population of cytotoxic T-cells with a population of antigen presenting cells in the presence and absence of the multispecific binding protein of claim 1, wherein the multispecific binding protein simultaneously and specifically binds to two cell surface co-stimulators or co-repressors on T-cells; and

b) measuring the amount of cytokine released from the population of T-cells, wherein an increase or decrease in amount of cytokine released in the presence of the multispecific binding, compared to the absence of the multispecific binding protein, identifies the multispecific binding protein as modulator of a T-cell response.

82. A method of modulating an immune response in a subject, the method comprising:

administering a therapeutic amount of the multispecific binding protein of claim 1 that simultaneously and specifically binds to a cell surface co-stimulator or co-repressor on an T-cell and to a cell surface antigen on a target cell, wherein the multispecific binding protein modulates a normal response of the T-cell to target cell binding.

3-5. -5. (canceled)

10. (canceled)

12. (canceled)

15-17. -17. (canceled)

19. (canceled)

26-27. -27. (canceled)

29. (canceled)

30. A therapeutic combination comprising:

a first multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, and a second binding site that specifically binds to an immune cell receptor complex component on the immune cell; and

a second multispecific binding protein comprising a first binding site that specifically binds to a target cell antigen, and a second binding site that specifically binds to a cell surface modulator on the immune cell.

31. The therapeutic combination of claim 30, wherein the target cell antigen is a disease-associated antigen.

32. The therapeutic combination of claim 30, wherein the target cell antigen is tumor-associated antigen.

41. The therapeutic combination of claim 30, wherein the first and/or second multispecific binding protein is a DVD-Ig, half-DVD-Ig, a scDVD-Ig, an fDVD-Ig, an rDVD-Ig, a pDVD-Ig, an mDVD-Ig or a coDVD-Ig.

42. The therapeutic combination of claim 30, wherein the first multispecific binding protein comprises a polypeptide chain having the formula VD1-(X1)n-VD2-C-(X2)n, wherein

VD1 is a first heavy chain variable domain;

VD2 is a second heavy chain variable domain;

C is a heavy chain constant domain;

X1 is a linker with the proviso that it is not CH1;

X2 is an Fc region;

(X1)n is (X1)0 or (X1)1;

(X2)n is (X2)0 or (X2)1; and

wherein

(a) VD1 or VD2 comprise a CDR region amino acid sequence selected from SEQ ID NO;

100, 101, 102;

106, 107, and 108;

(b) VD1 or VD2 comprises HCDR1-3 regions selected from the group consisting of SEQ ID NO;

100, 101, 102;

106, 107, and 108;

(c) VD1 and VD2 comprise HCDR1-3 regions selected from the group consisting of SEQ ID NO;

100, 101, 102;

106, 107, and 108;

(d) VD1 or VD2 comprise a VH amino acid sequence selected from the group consisting of SEQ ID NO;

84 and 86;

(e) VD1 and VD2 comprise SEQ ID NO;

84 and 86, respectively.

43. The therapeutic combination of claim 30, wherein the first multispecific binding protein comprises a polypeptide chain, wherein the polypeptide chain comprises VD1-(X1)n-VD2-C-(X2)n, wherein

VD1 is a first light chain variable domain;

VD2 is a second light chain variable domain;

C is a light chain constant domain;

X1 is a linker with the proviso that it is not CL;

X2 does not comprise an Fc region;

(X1)n is (X1)0 or (X1)1;

(X2)n is (X2)0 or (X2)1; and

wherein

(a) VD1 or VD2 comprise a CDR region amino acid sequence selected from SEQ ID NO;

103, 104, 105, 109, 110, and 111;

(b) VD1 or VD2 comprises LCDR1-3 regions selected from the group consisting of SEQ ID NO;

103, 104, and 105; and

109, 110, and 111;

(c) VD1 and VD2 comprise LCDR1-3 regions selected from the group consisting of SEQ ID NO;

103, 104, and 105; and

109, 110, and 111;

(d) VD1 or VD2 comprise a VL amino acid sequence selected from the group consisting of SEQ ID NO;

85, and 87;

(e) VD1 and VD2 comprise SEQ ID NO;

85 and 87, respectively.

44. The therapeutic combination of claim 30, wherein the second multispecific binding protein comprises a polypeptide chain having the formula VD1-(X1)n-VD2-C-(X2)n, wherein

VD1 is a first heavy chain variable domain;

VD2 is a second heavy chain variable domain;

C is a heavy chain constant domain;

X1 is a linker with the proviso that it is not CH1;

X2 is an Fc region;

(X1)n is (X1)0 or (X1)1;

(X2)n is (X2)0 or (X2)1; and

wherein

(a) VD1 or VD2 comprise a CDR region amino acid sequence selected from SEQ ID NO;

88, 89, 90;

94, 95, 96;

100, 101, and 102;

(b) VD1 or VD2 comprises HCDR1-3 regions selected from the group consisting of SEQ ID NO;

88, 89, and 90;

94, 95, and 96; and

100, 101, and 102;

(c) VD1 and VD2 comprise HCDR1-3 regions selected from the group consisting of SEQ ID NO;

88, 89, and 90;

94, 95, and 96; and

100, 101, and 102;

(d) VD1 or VD2 comprise a VH amino acid sequence selected from the group consisting of SEQ ID NO;

80, 82, and 84;

(e) VD1 and VD2 comprise SEQ ID NO;

80 and 84, respectively;

or

(f) VD2 and VD2 comprise SEQ ID NO;

82 and 84, respectively.

45. The therapeutic combination of claim 30, wherein the second multispecific binding protein comprises a polypeptide chain, wherein the polypeptide chain comprises VD1-(X1)n-VD2-C-(X2)n, wherein

VD1 is a first light chain variable domain;

VD2 is a second light chain variable domain;

C is a light chain constant domain;

X1 is a linker with the proviso that it is not CL;

X2 does not comprise an Fc region;

(X1)n is (X1)0 or (X1)1;

(X2)n is (X2)0 or (X2)1; and

wherein

(a) VD1 or VD2 comprise a CDR region amino acid sequence selected from SEQ ID NO;

91, 92, 93;

97, 98, 99;

103, 104, and 105;

(b) VD1 or VD2 comprises LCDR1-3 regions selected from the group consisting of SEQ ID NO;

91, 92, and 93;

97, 98, and 99; and

103, 104, and 105;

(c) VD1 and VD2 comprise LCDR1-3 regions selected from the group consisting of SEQ ID NO;

91, 92, and 93;

97, 98, and 99; and

103, 104, and 105;

(d) VD1 or VD2 comprise a VL amino acid sequence selected from the group consisting of SEQ ID NO;

81, 83, and 87;

(e) VD1 and VD2 comprise SEQ ID NO;

81 and 85, respectively;

or

(f) VD2 and VD2 comprise SEQ ID NO;

83 and 85, respectively.

33-40. -40. (canceled)

49-50. -50. (canceled)

51. A multispecific binding protein comprising:

a first binding site that specifically binds to a first T-cell modulator; and

a second binding site that specifically binds to a second T-cell modulator.

64. The multispecific binding protein of claim 51 which is a DVD-Ig, half-DVD-Ig, a scDVD-Ig, an fDVD-Ig, an rDVD-Ig, a pDVD-Ig, an mDVD-Ig or a coDVD-Ig.

65. The multispecific binding protein of claim 51, comprising a polypeptide chain having the formula VD1-(X1)n-VD2-C-(X2)n, wherein

VD1 is a first heavy chain variable domain;

VD2 is a second heavy chain variable domain;

C is a heavy chain constant domain;

X1 is a linker with the proviso that it is not CH1;

X2 is an Fc region;

(X1)n is (X1)0 or (X1)1;

(X2)n is (X2)0 or (X2)1; and

wherein

(a) VD1 or VD2 comprise a CDR region amino acid sequence selected from SEQ ID NO;

120, 121, 122, 126, 127, 128, 132, 134, 134, 138, 139, 140;

(b) VD1 or VD2 comprises HCDR1-3 regions selected from the group consisting of SEQ ID NO;

120, 121, and 122;

126, 127, and 128;

132, 134, and 134, and 138, 139, and 140;

(c) VD1 and VD2 comprise HCDR1-3 regions selected from the group consisting of SEQ ID NO;

120, 121, and 122;

126, 127, and 128;

132, 134, and 134, and 138, 139, and 140;

(d) VD1 or VD2 comprise a VH amino acid sequence selected from the group consisting of SEQ ID NO;

112, 114, 115, 116, 118;

(e) VD1 and VD2 comprise a VH amino acid sequence selected from the group consisting of SEQ ID NO;

112, 114, 115, 116, 118;

or

(f) the polypeptide chain comprises an amino acid sequence selected from the group consisting of SEQ ID NO;

144, 146, 148, 150, 152, 154, 156, and 158.

66. The multispecific binding protein of claim 51, comprising a polypeptide chain a polypeptide chain, wherein the polypeptide chain comprises VD1-(X1)n-VD2-C-(X2)n, wherein

VD1 is a first light chain variable domain;

VD2 is a second light chain variable domain;

C is a light chain constant domain;

X1 is a linker with the proviso that it is not CL;

X2 does not comprise an Fc region;

(X1)n is (X1)0 or (X1)1;

(X2)n is (X2)0 or (X2)1; and

wherein

(a) VD1 or VD2 comprise a CDR region amino acid sequence selected from SEQ ID NO;

123, 124, 125, 129, 130, 131, 135, 136, 137, 141, 142, 143;

(b) VD1 or VD2 comprises HCDR1-3 regions selected from the group consisting of SEQ ID NO;

123, 124, and 125;

129, 130, and 131;

135, 136, and 137; and

141, 142, and 143;

(c) VD1 and VD2 comprise HCDR1-3 regions selected from the group consisting of SEQ ID NO;

123, 124, and 125;

129, 130, and 131;

135, 136, and 137; and

141, 142, and 143;

(d) VD1 or VD2 comprise a VL amino acid sequence selected from the group consisting of SEQ ID NO;

113, 115, 117, and 119;

(e) VD1 and VD2 comprise a VL amino acid sequence selected from the group consisting of SEQ ID NO;

113, 115, 117, and 119;

or

(f) the polypeptide chain comprises an amino acid sequence selected from the group consisting of SEQ ID NO;

145, 147, 149, 151, 153, 155, 157, and 159.

67. A method of modulating the activation state of an immune cell, the method comprising contacting the immune cell with a multispecific binding protein of claim 51.

70. A method of directing a cytotoxic T-cell to lyse a target cell in a subject, the method comprising administering to the subject an effective amount of a multispecific binding protein of claim 51.

72. A method of reducing inflammation in a subject, the method comprising administering to the subject an effective amount of a multispecific binding protein of claim 51.

52-63. -63. (canceled)

68-69. -69. (canceled)

71. (canceled)

73. (canceled)