Variant activin receptor polypeptides, alone or in combination with chemotherapy, and uses thereof
The present invention provides variant activin IIB soluble receptor polypeptides and proteins capable of binding and inhibiting the activities of activin A, myostatin, or GDF-11. The present invention also provides polynucleotides, vectors and host cells capable of producing the variant polypeptides and proteins. Compositions and methods for treating muscle-wasting and other diseases and disorders are also provided.
1. A method of reducing the size of a gonadal tumor mass in a subject in need of such treatment comprising administering to the subject: an effective amount of an isolated protein comprising a variant activin IIB receptor polypeptide (vActRIIB) wherein vActRIIB comprises a polypeptide sequence having at least 99% identity to the amino acid sequence set forth at amino acids 25 through 134 of SEQ ID NO: 18, wherein the polypeptide comprises an amino acid substitution at position 28, wherein the substitution at position 28 is selected from the group of amino acids consisting of A, W, and Y for E, and wherein the polypeptide is capable of binding myostatin, activin A, or GDF-11; and a chemotherapeutic agent.
2. The method of claim 1 , wherein the tumor mass is an ovarian tumor mass.
3. The method of claim 1 , wherein the isolated protein and the chemotherapeutic agent are administered at the same time.
4. The method of claim 1 , wherein the isolated protein and the chemotherapeutic agent are each administered at different times.
5. The method of claim 1 , wherein the substitution at position 28 of the vActRIIB polypeptide is W.
6. The method of claim 1 , wherein the isolated protein further comprises an Fc domain linked to vActRIIB via a linker.
7. The method of claim 6 , wherein the sequence of the Fc domain is shown in SEQ ID NO:80, and wherein the sequence of the linker is shown in SEQ ID NO:79.
8. The method of claim 1 , wherein the isolated protein further comprises an IgG2 Fc domain linked to vActRIIB via a peptide linker.
9. The method of claim 1 , wherein the chemotherapeutic agent is a nucleoside analogue, 5-fluorouracil, and/or dacarbazine.
10. A method of treating a gonadal cancer in a subject in need of such treatment comprising administering to the subject: an effective amount of an isolated protein comprising a variant activin IIB receptor polypeptide (vActRIIB) wherein vActRIIB comprises a polypeptide sequence having at least 99% identity to the amino acid sequence set forth at amino acids 25 through 134 of SEQ ID NO: 18, wherein the polypeptide comprises an amino acid substitution at position 28, wherein the substitution at position 28 is selected from the group of amino acids consisting of A, W, and Y for E, and wherein the polypeptide is capable of binding myostatin, activin A, or GDF-11; and a chemotherapeutic agent.
11. The method of claim 10 , wherein the gonadal cancer is ovarian cancer.
12. The method of claim 10 , wherein the isolated protein and the chemotherapeutic agent are each administered at different times.
13. The method of claim 10 , wherein the isolated protein and the chemotherapeutic agent are administered at the same time.
14. The method of claim 10 , wherein the substitution at position 28 of the vActRIIB polypeptide is W.
15. The method of claim 10 , wherein the isolated protein further comprises an Fc domain linked to vActRIIB via a linker.
16. The method of claim 15 , wherein the sequence of the Fc domain is shown in SEQ ID NO:80, and wherein the sequence of the linker is shown in SEQ ID NO:79.
17. The method of claim 10 , wherein the isolated protein further comprises an Fc domain linked to vActRIIB via a linker.
18. The method of claim 10 , wherein the isolated protein further comprises an IgG2Fc domain linked to vActRIIB via a peptide linker.
19. The method of claim 10 , wherein the chemotherapeutic agent is a nucleoside analogue, 5-fluorouracil, and/or dacarbazine.