Methods for treating ulcers in thalassemia syndrome with an ActRIIB polypeptide
The present disclosure provides compositions and methods for treating or preventing ulcers in subjects having low red blood cell levels and/or hemoglobin levels (e.g, anemia). In some embodiments, the compositions of the disclosure may be used to treat or prevent ulcers associated with anemia.
1. A method for treating a cutaneous ulcer in a subject that has thalassemia syndrome, comprising administering to the subject a polypeptide comprising an amino acid sequence that is at least 85% identical to the sequence of amino acids 29-109 of SEQ ID NO: 1, wherein the polypeptide comprises and acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
2. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 90% identical to the sequence of amino acids 29-109 of SEQ ID NO:1, wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
3. The method of claim 1 , wherein the polypeptide is a fusion protein further comprising an immunoglobulin Fc domain.
4. The method of claim 3 , wherein the fusion protein further comprises a linker domain positioned between the polypeptide and the immunoglobulin Fc domain.
5. The method of claim 1 , wherein the polypeptide comprises one or more amino acid modifications selected from: a glycosylated amino acid, a PEGylated amino acid, a farnesylated amino acid, an acetylated amino acid, a biotinylated amino acid, and an amino acid conjugated to a lipid moiety.
6. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is 95% identical to amino acids 29-109 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
7. The method of claim 1 , wherein the polypeptide comprises amino acids 29-109 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
8. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 85% identical to the sequence of amino acids 25-131 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
9. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 90% identical to the sequence of amino acids 25-131 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
10. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 95% identical to the sequence of amino acids 25-131 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
11. The method of claim 1 , wherein the polypeptide comprises amino acids 25-131 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
12. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 85% identical to SEQ ID NO: 44, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
13. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 90% identical to SEQ ID NO: 44, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
14. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 95% identical to SEQ ID NO: 44, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.
15. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 44, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79of SEQ ID NO: 1.
16. The method of claim 1 , wherein the polypeptide inhibits signaling by GDF8 in a cell-based assay.
17. The method of claim 1 , wherein the polypeptide inhibits signaling by GDF11 in a cell-based assay.
18. The method of claim 1 , wherein the amino acid at the position corresponding to position 79 of SEQ ID NO: 1 is an aspartic acid.
19. The method of claim 1 , wherein the amino acid at the position corresponding to position 79 of SEQ ID NO:1 is a glutamic acid.
20. The method of claim 1 , wherein the patient has a β-thalassemia syndrome.
21. The method of claim 20 , wherein the patient has β-thalassemia minor.
22. The method of claim 20 , wherein the patient has β-thalassemia intermedia.
23. The method of claim 20 , wherein the patient has β-thalassemia major.
24. The method of claim 1 , wherein the patient has alpha-thalassemia syndrome.
25. The method of claim 1 , wherein the polypeptide binds GDF8.
26. The method of claim 1 , wherein the polypeptide binds GDF11.