Methods of treating inflammation with monomeric CXCL12 peptide
The present invention provides a CXCL12 1 peptide engineered to resist peptide-induced dimerization by maintaining steric repulsion of the chemokine helix, pharmaceutical compositions thereof, and methods of using said dimer in the treatment of cancer, inflammatory disorders, autoimmune disease, and HIV/AIDS.
1. A method of reducing inflammation in a subject suffering from inflammation, the method comprising administering to the subject a therapeutically effective amount of a composition comprising a constitutively monomeric CXCL12 peptide comprising the amino acid sequence of SEQ ID NO:1 wherein the amino acids at positions 55 and 58 are substituted with cysteine.
2. The method of claim 1 , wherein CXCL12 peptide is CXCL12 1 having the amino acid sequence of SEQ ID NO:2.
3. The method of claim 1 , wherein the inflammation is associated with a disease selected from the group consisting of Multiple Sclerosis (MS), Guillain-Barre Syndrome, Amyotrophic Lateral Sclerosis, Parkinson's disease, Alzheimer's disease, Type I diabetes, lupus, ankylosing spondylitis, rheumatoid arthritis, psoriatic arthritis, juvenile arthritis, early arthritis, reactive arthritis, osteoarthritis, ankylosing spondylitis, autoimmune uveitis, and inflammatory bowel diseases.
4. The method of claim 1 , wherein the subject has inflammation associated with Type I diabetes.
5. The method of claim 4 , wherein the subject is a human.
6. The method of claim 1 , wherein the subject is a mammal.
7. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable carrier or diluent.