Antibodies which specifically bind to canine vascular endothelial growth factor and uses thereof
View Patent ↗Disclosed herein are antibodies capable of inhibiting canine vascular endothelial growth factor and uses thereof in treating a canine angiogenesis-related disorder such as a proliferative disease.
1. An isolated antibody that binds a canine vascular endothelial growth factor (VEGF), wherein the antibody comprises
(i) a heavy chain that includes a heavy chain complementarity determining region 1 (HC CDR1) set forth as SEQ ID NO: 5, a heavy chain complementarity determining region 2 (HC CDR2) set forth as SEQ ID NO: 6, and a heavy chain complementarity determining region 3 (HC CDR3) set forth as SEQ ID NO: 7, and
(ii) a light chain that includes a light chain complementarity determining region 1 (LC CDR1) set forth as SEQ ID NO: 8, a light chain complementarity determining region 2 (LC CDR2) set forth as SEQ ID NO: 9, and a light chain complementarity determining region 3 (LC CDR3) set forth as SEQ ID NO: 10.
2. The isolated antibody of claim 1 , wherein the heavy chain comprises a heavy chain variable region that comprises the amino acid sequence of SEQ ID NO: 2.
3. The isolated antibody of claim 2 , wherein the light chain comprises a light chain variable region that comprises the amino acid sequence of SEQ ID NO: 4.
4. The isolated antibody of claim 1 , wherein the light chain comprises a light chain variable region that comprises the amino acid sequence of SEQ ID NO: 4.
5. The isolated antibody of claim 1 , wherein the antibody is a full length antibody or an antigen-binding fragment thereof.
6. The isolated antibody of claim 1 , wherein the antibody is a canine antibody or a caninized antibody.
7. A pharmaceutical composition comprising the antibody of claim 1 and a pharmaceutically acceptable carrier.
8. A method for inhibiting VEGF in a canine subject, comprising administering to a canine subject in need thereof an effective amount of an antibody of claim 1 .
9. The method of claim 8 , wherein the antibody comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 2, and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 4.
10. The method of claim 8 , wherein the antibody is a full length antibody or an antigen-binding fragment thereof.
11. The method of claim 8 , wherein the canine subject has or is suspected of having an angiogenesis-related disease.
12. The method of claim 11 , wherein the canine subject has an angiogenesis-related disease is selected from the group consisting of a proliferative disease, macular degeneration, age-related macular degeneration, diabetic retinopathy, retinal detachment, glaucoma, pterygium of the conjunctiva and cornea, neuomyelitis optica, corneal neovascularization, neoplastic meningitis, myelofibrosis, radiation necrosis, and keloid.
13. The method of claim 11 , wherein the angiogenesis-related disease is cancer.
14. The method of claim 13 , wherein the cancer is selected from the group consisting of glioblastoma, sarcoma, hepatocellular carcinoma, inflammatory breast carcinoma pancreatic cancer, metastatic melanoma, ovarian cancer, high-risk neuroblastoma, esophageal cancer, gastric cancer, metastatic head tumor, metastatic neck tumor, cervical cancer, peritoneal cancer, and squamous cell carcinoma.
15. The method of claim 13 , further comprising administering to the canine subject a chemotherapeutic agent.