Methods and compositions for modulating angiogenesis and pericyte composition

Patent metadata

Field	Value
Publication number	US-2022017600-A1
Application number	US-202117184692-A
Country	US
Kind code	A1
Filing date	Feb 25, 2021
Priority date	Nov 2, 2006
Publication date	Jan 20, 2022
Grant date	—

Abstract

In certain aspects, the present disclosure relates to the insight that a polypeptide comprising a ligand-binding portion of the extracellular domain of activin-like kinase I (ALK1) polypeptide may be used to inhibit angiogenesis in vivo, particularly in mammals suffering angiogenesis-related disorders. Additionally, the disclosure demonstrates that inhibitors of ALK1 may be used to increase pericyte coverage in vascularized tissues, including tumors and the retina. The disclosure also identifies ligands for ALK1 and demonstrates that such ligands have pro-angiogenic activity, and describes antibodies that inhibit receptor-ligand interaction.

First claim

1 .- 8 . (canceled)

9 . A method for inhibiting angiogenesis in a mammal in need thereof, the method comprising administering to the mammal an effective amount of a pharmaceutical preparation comprising an ALK1-Fc fusion protein comprising: a polypeptide having an amino acid sequence that is at least 97% identical to the sequence of amino acids 22-118 of SEQ ID NO:1, which polypeptide is fused to an Fc portion of an immunoglobulin, and wherein the ALK1-Fc fusion protein binds to GDF5, GDF7 and BMP9 with a K D of less than 1×10 −7 M and binds to TGFβ-1 with a K D of greater than 1×10 −6 , and wherein at least 90% of the ALK1-Fc fusion protein is present in a dimeric form.

10 .- 12 . (canceled)

13 . The method of claim 9 , wherein the method further comprises administering a second agent that inhibits angiogenesis.

14 . A method of promoting an increase in pericyte coverage in a vascularized tissue of a mammal in need thereof, the method comprising administering to the mammal an effective amount of an ALK1 ECD protein.

15 . The method of claim 14 , wherein the ALK1 ECD protein is an ALK1-Fc fusion protein.

16 . The method of claim 15 , wherein the ALK1-Fc fusion protein comprises a polypeptide having an amino acid sequence that is at least 90% identical to the sequence of amino acids 22-118 of SEQ ID NO:1, which polypeptide is fused to an Fc portion of an immunoglobulin, and wherein the ALK1-Fc fusion protein binds to TGFβ-1 with a KD of greater than 1×10 −6 .

17 . The method of claim 14 , wherein the ALK1 ECD protein binds to one or more ALK1 ligands selected from the group consisting of: GDF5, GDF6, GDF7, BMP9 and BMP10.

18 . The method of claim 14 , wherein the ALK1 ECD polypeptide comprises an amino acid sequence that is at least 90% identical to the sequence of amino acids corresponding to amino acids 34-95 of SEQ ID NO:1.

19 . The method of claim 14 , wherein the ALK1 ECD comprises an amino acid sequence encoded by a nucleic acid that hybridizes under stringent hybridization conditions to nucleotides 100-285 of SEQ ID NO:2 or a variant of nucleotides 100-285 of SEQ ID NO:2 that encodes the same amino acid sequence.

20 . The method of claim 15 , wherein the ALK1-Fc fusion protein has a sequence of SEQ ID NO:3.

21 . The method of claim 15 , wherein the ALK1-Fc fusion protein is administered in a pharmaceutical preparation wherein at least 90% of the ALK1-Fc fusion protein is in a dimeric form.

22 . The method of claim 14 , wherein the ALK1 ECD fusion protein is delivered intravenously or locally to the eye.

23 . The method of claim 14 , wherein the method further comprises administering a second agent that inhibits angiogenesis.

24 . The method of claim 14 , wherein the vascularized tissue is selected from the group consisting of: the eye of the mammal, a tumor, a bone and a joint.

25 . The method of claim 14 , wherein the mammal has diabetic retinopathy or other retinal disorder characterized by a loss of pericyte coverage in the retinal vasculature.

26 . The method of claim 14 , wherein the mammal has a tumor selected from the group consisting of: melanoma, a lung tumor, multiple myeloma and breast cancer.

27 . The method of claim 14 , wherein the mammal has a pancreatic tumor.

28 . The method of claim 27 , wherein the mammal has a tumor of the pancreatic endocrine tissue.

29 .- 39 . (canceled)

40 . A method for treating a tumor in a mammal, the method comprising, administering to a mammal that has a tumor an effective amount of an agent selected from the group consisting of:
(a) an ALK1 ECD protein; (b) an antibody that binds to an ALK1 ligand and inhibits the binding of the ALK1 ligand to ALK1, wherein the ALK1 ligand is selected from the group consisting of GDF5, GDF6, GDF7, BMP9 and BMP10; (c) an antibody that binds to an ALK1 polypeptide consisting of amino acids 22-118 of SEQ ID NO:1 and inhibits the binding of at least one ALK1 ligand selected from the group consisting of: GDF5, GDF6, GDF7, BMP9 and BMP10; and (d) a DAN polypeptide,
wherein the tumor is selected from the group consisting of: melanoma, multiple myeloma, a tumor associated with bone, a tumor that has metastasized to bone, a lung tumor, a pancreatic tumor and breast cancer.

41 . The method of claim 40 , wherein the ALK-1 ECD protein is an ALK1-Fc fusion protein.

42 . The method of claim 41 , wherein the ALK1-Fc fusion protein comprises a polypeptide having an amino acid sequence that is at least 90% identical to the sequence of amino acids 22-118 of SEQ ID NO:1, which polypeptide is fused to an Fc portion of an immunoglobulin, and wherein the ALK1-Fc fusion protein binds to TGFβ-1 with a K D of greater than 1×10 −6 .

43 .- 60 . (canceled)

Assignees

• Acceleron Pharma Inc
• Ludwig Inst For Cancer Res Ltd

Inventors

• Grinberg Asya
• Knopf John
• Pearsall Robert S
• Kumar Ravindra
• Seehra Jasbir
• Pietras Kristian

Classifications

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title

• C07K2319/30

  Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto · CPC title

• C07K2319/32

  fusions with soluble part of a cell surface receptor, "decoy receptors" · CPC title

• A61P27/02

  Ophthalmic agents · CPC title

• C07K14/71 Primary

  for growth factors; for growth regulators · CPC title