Humanized anti-hepcidin antibodies and uses thereof
The present application relates to humanized antibodies that specifically bind to hepcidin and methods of using the humanized antibodies. Another aspect relates to humanized antibodies which bind hepcidin and regulate iron homeostasis. Another aspect relates to the use of humanized antibodies which bind hepcidin for the treatment of a disease or condition associated with hepcidin.
1. A humanized antibody, or antigen-binding fragment thereof, that specifically binds to hepcidin (Hep), that comprises a heavy chain variable region having an amino acid sequence set forth as SEQ ID NO: 43, 46, or 48; and a light chain variable region having an amino acid sequence set forth as SEQ ID NO: 50, 52, 54, or 55.
2. A humanized antibody, or antigen-binding fragment thereof, that specifically binds to hepcidin, that comprises a heavy chain variable region having an amino acid sequence set forth as SEQ ID NO: 43 and a light chain variable region having an amino acid sequence set forth as SEQ ID NO: 50.
3. A humanized antibody, or antigen-binding fragment thereof, that specifically binds to hepcidin, that comprises a heavy chain variable region having an amino acid sequence set forth as SEQ ID NO: 43 and a light chain variable region having an amino acid sequence set forth as SEQ ID NO: 54.
4. A humanized antibody, or antigen-binding fragment thereof, that specifically binds to hepcidin, that comprises a heavy chain variable region having an amino acid sequence set forth as SEQ ID NO: 48 and a light chain variable region having an amino acid sequence set forth as SEQ ID NO: 52.
5. A humanized antibody, or antigen-binding fragment thereof, that specifically binds to hepcidin, that comprises a heavy chain variable region having an amino acid sequence set forth as SEQ ID NO: 43 and a light chain variable region having an amino acid sequence set forth as SEQ ID NO: 55.
6. A humanized antibody, or antigen-binding fragment thereof, that specifically binds to hepcidin, that comprises a heavy chain variable region having an amino acid sequence set forth as SEQ ID NO: 46 and a light chain variable region having an amino acid sequence set forth as SEQ ID NO: 50.
7. A humanized antibody, or antigen-binding fragment thereof, that specifically binds to hepcidin, that comprises a heavy chain variable region having an amino acid sequence set forth as SEQ ID NO: 46 and a light chain variable region having an amino acid sequence set forth as SEQ ID NO: 52.
8. The humanized antigen-binding fragment of claim 1 , wherein the antigen-binding fragment is a Fab fragment, a Fab′ fragment, a F(ab′) 2 fragment, a Fv fragment, a scFv fragment, or a single chain binding polypeptide.
9. A method of treating a disorder of iron homeostasis associated with elevated hepcidin levels in a subject in need thereof, comprising administering to the subject an antibody, or an antigen-binding fragment thereof, of claim 1 .
10. The method of claim 9 , wherein the disorder of iron homeostasis comprises an anemia.
11. The method of claim 10 , wherein the anemia comprises an iron refractory iron deficiency anemia (IRIDA), an Anemia of Chronic Disease (ACD), an Anemia of Cancer, an Anemia of Inflammation, a Congenital Dyserythropoietic Anemia, or a Chemotherapy Induced Anemia (CIA).
12. A method of diagnosing a disorder of iron homeostasis associated with elevated hepcidin levels in a subject, comprising:
a. detecting whether hepcidin is present in a biological sample obtained from the subject by contacting the sample with an antibody, or an antigen-binding fragment thereof, of claim 1 , and detecting binding between hepcidin and the antibody or the antigen-binding fragment thereof; and
b. diagnosing the subject with a disorder of iron homeostasis associated with elevated hepcidin levels when the amount of hepcidin bound to the antibody, or the antigen-binding fragment thereof, is greater than a predetermined threshold.
13. The method of claim 12 , wherein the disorder of iron homeostasis comprises an anemia.
14. The method of claim 13 , wherein the anemia comprises an iron refractory iron deficiency anemia (IRIDA), an Anemia of Chronic Disease (ACD), an Anemia of Cancer, an Anemia of Inflammation, a Congenital Dyserythropoietic Anemia, or a Chemotherapy Induced Anemia (CIA).
15. The method of claim 12 , further comprising administering the antibody, or the antigen-binding fragment thereof, to the subject when the amount of hepcidin bound to the antibody, or the antigen-binding fragment thereof, is greater than the predetermined threshold.
16. A container that comprises an antibody, or an antigen-binding fragment thereof, of claim 1 , wherein the container comprises a vial, a syringe, a bottle, an intravenous bag, or an ampoule.
17. A kit for treating a disorder associated with elevated hepcidin levels or a disorder of iron homeostasis associated with elevated hepcidin levels, that comprises an antibody, or an antigen-binding fragment thereof, of claim 1 , and a label attached to, or packaged within, the kit; the label describing use of the antibody, or the antigen-binding fragment thereof.
18. The kit of claim 17 , that further comprises an erythropoiesis stimulator.
19. A kit for diagnosing a disorder associated with elevated hepcidin levels or a disorder of iron homeostasis associated with elevated hepcidin levels, that comprises an antibody, or an antigen-binding fragment thereof, of claim 1 , and a label attached to, or packaged within, the kit; the label describing use of the antibody, or the antigen-binding fragment thereof.
20. The kit of claim 19 , wherein the label describes use of the antibody, or the antigen-binding fragment thereof, to diagnose a subject having a level of hepcidin in a physiologically normal range, but elevated relative to a plasma iron level, or to a percentage of transferrin saturation (% TSAT).