US2023212261A1PendingUtilityA1

Isolated polypeptides of cd44 and uses thereof

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Assignee: YISSUM RES DEV CO OF HEBREW UNIV JERUSALEM LTDPriority: Jul 15, 2014Filed: Dec 20, 2022Published: Jul 6, 2023
Est. expiryJul 15, 2034(~8 yrs left)· nominal 20-yr term from priority
A61K 38/177A61P 19/02A61P 29/00C07K 14/70585A61K 38/00A61P 17/06A61P 25/28A61P 35/00A61P 43/00A61P 9/00G01N 33/5044C07K 2319/00
69
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Claims

Abstract

Isolated polypeptides of CD44 are provided. Accordingly, there is provided an isolated polypeptide consisting of an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-3. Also provided is an isolated end-capping modified polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 1-3, wherein the modified polypeptide comprises an anti-inflammatory activity. Also provided are compositions of matter, fusion proteins and pharmaceutical compositions and their use in the treatment of inflammatory disease.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating an inflammatory disease in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a 5 amino acid peptide consisting of SEQ ID NO: 1, thereby treating the inflammatory disease in the subject. 
     
     
         2 . A method of treating an inflammatory disease in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a 5 amino acid peptide modified at the N— and/or C— terminus, wherein the peptide consists of SEQ ID NO: 1 and has an anti-inflammatory activity, thereby treating the inflammatory disease in the subject. 
     
     
         3 . The method of  claim 2 , wherein said peptide is modified at the N terminus with an Acetyl. 
     
     
         4 . The method of  claim 2 , wherein said peptide is modified at the C terminus with an Amide. 
     
     
         5 . The method of  claim 2 , wherein said peptide is modified at the N-terminus with an Acetyl and at the C-terminus with an Amide as set forth in SEQ ID NO: 4. 
     
     
         6 . The method of  claim 1 , wherein said peptide is attached to a non-proteinaceous moiety. 
     
     
         7 . The method of  claim 6 , wherein said attached is covalent attachment. 
     
     
         8 . The method of  claim 2 , wherein said peptide is attached to a non-proteinaceous moiety. 
     
     
         9 . The method of  claim 8 , wherein said attached is covalent attachment. 
     
     
         10 . The method of  claim 2 , wherein said anti-inflammatory activity is not dependent on vaccination or mucosal tolerance. 
     
     
         11 . The method of  claim 2 , wherein said peptide is capable of binding a protein selected from the group consisting of serum amyloid A, Transthyretin and apolipoprotein B. 
     
     
         12 . The method of  claim 1 , wherein said administering comprises oral administering. 
     
     
         13 . The method of  claim 2 , wherein said administering comprises oral administering. 
     
     
         14 . The method of  claim 1 , wherein said inflammatory disease is a neurodegenerative disease. 
     
     
         15 . The method of  claim 2 , wherein said inflammatory disease is a neurodegenerative disease. 
     
     
         16 . The method of  claim 1 , wherein said inflammatory disease is cancer. 
     
     
         17 . The method of  claim 2 , wherein said inflammatory disease is cancer.

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