Nogo receptor binding protein
View Patent ↗The invention provides Sp35 polypeptides and fusion proteins thereof, Sp35 antibodies and antigen-binding fragments thereof and nucleic acids encoding the same. The invention also provides compositions comprising, and methods for making and using, such Sp35 antibodies, antigen-binding fragments thereof, Sp35 polypeptides and fusion proteins thereof.
1. A method of treating a CNS disease, disorder or injury associated with neurodegeneration in a mammal in need thereof comprising administering to said mammal a therapeutically effective amount of an Sp35 antagonist.
2. The method of claim 1 , wherein the Sp35 antagonist is a soluble fragment of SEQ ID NO:2.
3. The method of claim 2 , wherein the soluble fragment of SEQ ID NO:2 is selected from the group consisting of:
(a) a polypeptide comprising amino acids 34-532 of SEQ ID NO:2;
(b) a polypeptide comprising amino acids 34-417 of SEQ ID NO:2;
(c) a polypeptide comprising amino acids 34-432 of SEQ ID NO:2;
(d) a polypeptide comprising amino acids 417-531 of SEQ ID NO:2;
(e) a polypeptide comprising amino acids 425-531 of SEQ ID NO:2;
(f) a polypeptide comprising amino acids 1-531 of SEQ ID NO:2;
(g) a polypeptide comprising amino acids 433-493 of SEQ ID NO:2;
(h) a polypeptide comprising an Sp35 LRR domain, an Sp35 basic region C-terminal to the LRR domain, and an Sp35 immunoglobulin (Ig) domain C-terminal to the basic region, but lacks a transmembrane domain;
(i) a polypeptide comprising an Sp35 Ig domain, but lacking an Sp35 LRR domain, an Sp35 basic region, a transmembrane domain, and a cytoplasmic domain;
(j) a polypeptide comprising an Sp35 LRR domain, but lacking an Sp35 Ig domain, an Sp35 basic region, a transmembrane domain, and a cytoplasmic domain;
(k) a polypeptide as in (h), further lacking a cytoplasmic domain; and
(l) a polypeptide consisting of the amino acids of SEQ ID NO:10 (LSPRKH).
4. The method of claim 2 , wherein the soluble fragment of SEQ ID NO:2 is conjugated to a polymer.
5. The method of claim 4 , wherein the polymer is selected from the group consisting of polyalkylene glycol, a sugar polymer, and a heterologous polypeptide.
6. The method of claim 5 , wherein the heterologous polypeptide is selected from the group consisting of: an Ig polypeptide, a serum albumin polypeptide, a targeting polypeptide, a reporter polypeptide, a human NgR1-binding polypeptide, one or more cysteine residues and a purification-facilitating polypeptide.
7. The method of claim 6 , wherein the Ig polypeptide is an Fc polypeptide.
8. The method of claim 1 , wherein the Sp35 antagonist is an Sp35 antibody.
9. The method of claim 8 , wherein said CNS disease, disorder or injury is multiple sclerosis.
10. The method of claim 1 , wherein said CNS disease, disorder, or injury is selected from the group consisting of multiple sclerosis, ALS, Huntington's disease, Alzheimer's disease, Parkinson's disease, diabetic neuropathy, stroke, traumatic brain injury, optic nerve injury and spinal cord injury.
11. The method of claim 1 , wherein the Sp35 antagonist is administered locally.
12. A method of treating spinal cord injury in a mammal in need thereof comprising administering to said mammal a therapeutically effective amount of an Sp35 antagonist.
13. A method of treating optic nerve injury in a mammal in need thereof comprising administering to said mammal a therapeutically effective amount of an Sp35 antagonist.
14. A method of treating multiple sclerosis in a mammal in need thereof comprising administering to said mammal a therapeutically effective amount of an Sp35 antagonist.
15. A method of treating CNS disease, disorder or injury associated with neurodegeneration in a mammal in need thereof comprising administering to said mammal a therapeutically effective amount of an interfering RNA molecule, wherein said interfering RNA molecule inhibits the expression of Sp35.
16. The method of claim 15 , wherein the interfering RNA molecule comprises a nucleic acid sequence selected from the group consisting of SEQ ID NO: 41 and SEQ ID NO: 42.