Method of treating an inflammatory bowel disease comprising agonists of orexin-1 receptor
The present invention relates to methods and pharmaceutical compositions for the treatment of inflammatory bowel diseases. The presents methods relates to a method of treating an inflammatory bowel disease in a subject in need thereof comprising administering the subject with a therapeutically effective amount of at least one OX1R agonist.
1. A method of treating an inflammatory bowel disease in a subject in need thereof comprising administering to the subject at least one OX1R agonist in an amount sufficient to reduce secretion of a pro-inflammatory cytokine in cells of the subject, wherein the OX1R agonist is a polypeptide selected from the group consisting of SEQ ID NO:2, a polypeptide having at least 70% of identity with SEQ ID NO:3, and a polypeptide having at least 70% of identity with SEQ ID NO:4.
2. The method of claim 1 wherein the inflammatory bowel disease is ulcerative colitis, Crohn's disease, microscopic colitis, infectious colitis caused by bacteria or by virus, radiation colitis, ischemic colitis, pediatric colitis, undetermined colitis, and functional bowel disorders without evident anatomical abnormalities.
3. The method of claim 2 , wherein the Crohn's disease specifically affects the colon either with ileitis or without ileitis.
4. The method of claim 1 wherein the OX agonist is selected from the group consisting of small organic molecules, antibodies, aptamers and polypeptides.
5. The method of claim 1 wherein the OX1R agonist is a polypeptide selected from the group consisting of SEQ ID NO:3 and SEQ ID NO:4.
6. The method of claim 1 wherein the is fused to a Fc domain to form an immunoadhesin.
7. The method of claim 1 wherein the OX1R agonist is administered to the subject in combination with a standard treatment selected from the group consisting of corticosteroids, immunosuppressive drugs, aminosalicylates, immunosuppressors and biological treatments.
8. The method of claim 7 , wherein the aminosalicylate is Mesalazine, Sulfasalazine, Balsalazide, or Olsalazine.
9. The method of claim 7 , wherein the immunosuppressor is azathioprine, 6-mercaptopurine, methotrexate, rapamycine, cyclosporine or tacrolimus.
10. The method of claim 7 , wherein the biological treatment is Infliximab, Visilizumab, Adalimumab, Vedolizumab, golimumab or tofacitinib.
11. The method of claim 1 , wherein the pro-inflammatory cytokine is TNFα.