US2009148507A1PendingUtilityA1
Chimeric polypeptides containing chemokine domains
Est. expiryFeb 28, 2017(expired)· nominal 20-yr term from priority
A61P 31/18A61P 43/00A61P 37/02A61P 37/04A61K 39/3955C07K 14/522A61K 38/00C07K 2319/00A61K 47/6813A61K 47/6835C07K 2319/30A61P 29/00C07K 14/523
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Claims
Abstract
This invention provides a chimeric DNA molecule comprising a sequence encoding a chemokine polypeptide covalently attached to a heterologous polypeptide, the encoded chimeric polypeptide, and uses thereof.
Claims
exact text as granted — not AI-modified1 - 56 . (canceled)
57 . A method for altering CXCR4 receptor function in a subject in need thereof comprising administering to said subject a therapeutically effective amount of a composition comprising a chimeric polypeptide and a pharmaceutically acceptable carrier, wherein said chimeric polypeptide comprises
at least one chemokine polypeptide covalently attached to at least one heterologous polypeptide, and wherein the heterologous polypeptide is an Fc polypeptide, wherein the chemokine polypeptide comprises SEQ ID NO:1 from amino acid 22 to amino acid 328.
58 . The method of claim 57 , wherein said composition is in the form of a liposome.
59 . The method of claim 57 , further comprising administering a cytokine, a lymphokine, a hematopoietic factor, a thrombolytic factor, or an anti-thrombolytic factor.
60 . The method of claim 57 , wherein said composition is administered orally, topically, by inhalation, or by cutaneous, subcutaneous, intraperitoneal, parenteral, or intravenous injection.
61 . The method of claim 60 , wherein said composition is administered orally in the form of a tablet, capsule, powder, solution or elixir.
62 . The method of claim 57 , wherein said composition comprises about 0.01 ng to about 100 mg of chimeric polypeptide per kg body weight.
63 . A method for inhibiting binding of a CXCR4 receptor to a CXCR4 receptor ligand comprising contacting a cell expressing said receptor with a chimeric polypeptide in an amount effective to inhibit binding of said receptor to said ligand, wherein said chimeric polypeptide comprises at least one chemokine polypeptide covalently attached to at least one heterologous polypeptide, and wherein the heterologous polypeptide is an Fc polypeptide, wherein the chemokine polypeptide comprises SEQ ID NO:1 from amino acid 22 to amino acid 328.
64 . The method of claim 63 , wherein said chimeric polypeptide is administered to a subject in vivo.
65 . The method of claim 63 , wherein said cell is contacted with said chimeric polypeptide in vitro.
66 . The method of claim 64 , wherein said chimeric polypeptide is in the form of a liposome.
67 . The method of claim 64 , further comprising administering a cytokine, a lymphokine, a hematopoietic factor, a thrombolytic factor, or an anti-thrombolytic factor.
68 . The method of claim 64 , wherein said chimeric polypeptide is administered orally, topically, by inhalation, or by cutaneous, subcutaneous, intraperitoneal, parenteral, or intravenous injection.
69 . The method of claim 68 , wherein said chimeric polypeptide is administered orally in the form of a tablet, capsule, powder, solution or elixir.
70 . The method of claim 64 , wherein said chimeric polypeptide comprises about 0.01 μg to about 100 mg of chimeric polypeptide per kg body weight.Cited by (0)
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