Compositions and methods for treatment of bone associated diseases
US-2021403514-A1 · Dec 30, 2021 · US
US11976099B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11976099-B2 |
| Application number | US-202117393593-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 4, 2021 |
| Priority date | Aug 18, 2016 |
| Publication date | May 7, 2024 |
| Grant date | May 7, 2024 |
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Mutant M-CSF protein, comprising α v β 3 integrin binding motif and pharmaceutical compositions comprising same, are provided. Further, use of the composition for the treatment and or prevention of diseases associated with increased bone resorption are provided.
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The invention claimed is: 1. A polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 16, and SEQ ID NO: 19, wherein said polypeptide is characterized by antagonizing c-FMS and/or impairing osteoclast differentiation, and wherein said polypeptide may be further characterized by having diminished non-covalent dimerization. 2. The polypeptide of claim 1 , wherein said polypeptide comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 16 and SEQ ID NO: 19, and wherein residues 25-32 of said SEQ ID NO: 16 or SEQ ID NO: 19 is an RGD motif selected from the group consisting of: SEQ ID NO: 8 (QTRGDSPS), SEQ ID NO: 9 (TYPRGDMCS), and SEQ ID NO: 10 (EPVRGDNIN). 3. An isolated nucleic acid molecule encoding the polypeptide of claim 1 . 4. An expression vector comprising the nucleic acid of claim 3 . 5. A cell transformed or transfected with the expression vector of claim 4 . 6. A pharmaceutical composition comprising the polypeptide of claim 1 and a pharmaceutical acceptable carrier. 7. A method for treating a disease characterized by excessive osteoclast differentiation or increased bone resorption in a subject in need thereof, the method comprising the step of administering to said subject a therapeutically effective amount of a pharmaceutical composition comprising the polypeptide of claim 1 and a pharmaceutical acceptable carrier, thereby treating a disease characterized by excessive osteoclast differentiation or increased bone resorption in a subject in need thereof. 8. The method of claim 7 , wherein said disease associated with increased bone resorption is osteoporosis.
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