US2023212261A1PendingUtilityA1
Isolated polypeptides of cd44 and uses thereof
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
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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-modifiedWhat 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.Cited by (0)
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