Use of Sdf-1 for the Treatment and/or Prevention of Neurological Diseases
The invention relates to the use of SDF-1, or of an agonist of SDF-1 activity, for the treatment and/or prevention of a neurological disease.
1 - 28 . (canceled)
29 . A method of treating a neurological disease comprising the administration of a pharmaceutical composition comprising SDF-1 or naturally occurring isoforms thereof to an individual in an amount sufficient to treat said neurological disease, wherein said neurological disease is selected from the group consisting of traumatic nerve injury, stroke, peripheral neuropathy, diabetic neuropathy, neuropathic pain, multiple sclerosis (MS), primary progressive multiple sclerosis (MS), secondary progressive multiple sclerosis (MS), chronic inflammatory multiple sclerosis, demyelinating polyneuropathy (CIDP) or Guillain-Barré syndrome (GBS).
30 . The method of claim 29 , wherein SDF-1 is selected from the group consisting of:
(a) a polypeptide comprising amino acids of SEQ ID NO: 1;
(b) a polypeptide comprising amino acids of SEQ ID NO: 4;
(c) a polypeptide comprising amino acids of SEQ ID NO: 7; and
(d) a polypeptide of (a) to (c) further comprising a signal sequence.
31 . The method of claim 29 , wherein SDF-1 is fused to a carrier molecule, a peptide or a protein that promotes the crossing of the blood brain barrier.
32 . The method of claim 29 , wherein SDF-1 is PEGylated.
33 . The method of claim 29 , wherein the fused protein comprises an immunoglobulin (Ig) fusion.
34 . The method of claim 29 , wherein said composition further comprises an interferon and/or osteopontin and/or clusterin.
35 . The method of claim 34 , wherein the interferon is interferon-β.
36 . The method of claim 29 , wherein SDF-1 is administered in an amount of about 0.001 to 1 mg/kg of body weight, or about 0.01 to 10 mg/kg of bodyweight or about 9, 8, 7, 6, 5, 4, 3, 2 or 1 mg/kg of body weight or about 0.1 to 1 mg/kg of body weight to said individual.