Methods and Systems for Designing and/or Characterizing Soluble Lipidated Ligand Agents
US-2019135882-A1 · May 9, 2019 · US
US11197906B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11197906-B2 |
| Application number | US-201716070467-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 23, 2017 |
| Priority date | Jan 22, 2016 |
| Publication date | Dec 14, 2021 |
| Grant date | Dec 14, 2021 |
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The present disclosure relates to, among other things, compositions and methods for treating an inflammatory condition including, but not limited to, ocular inflammation, dry eye disease, and ocular neuropathic pain. One aspect of the present disclosure relates to a composition comprising (a) chemerin or a fragment or analog thereof and (b) a lipid entity linked to the chemerin or fragment or analog thereof.
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What is claimed is: 1. A method of decreasing blink reflex in a human subject having dry eye disease, the method comprising topically administering to an eye of the human subject a therapeutically effective amount of a composition, thereby decreasing the blink reflex, wherein the composition comprises: a chemerin fragment consisting of the sequence of Y-F-P-G-Q-F-A-F-S(SEQ ID NO.: 2) or a chemerin analog consisting of the sequence of Y*-F-L-P-S*-Q-F-A*-Tic-S (SEQ ID NO.: 3), wherein * denotes D amino acids and Tic represents 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid; a lipid entity linked to the chemerin fragment or chemerin analog, wherein the lipid entity is selected from the group consisting of α-linolenic acid, γ-linolenic acid, palmitic acid, vaccenic acid, oleic acid, and elaidic acid; and a linker connecting the lipid entity to the chemerin fragment or chemerin analog, wherein the linker comprises polyethylene glycol, KGG, or a combination thereof. 2. The method of claim 1 , wherein the composition is administered once a day, twice a day, or thrice a day. 3. The method of claim 1 , wherein the composition is formulated for topical administration as eye drops. 4. The method of claim 1 , wherein the lipid entity is linked at or near the N-terminus of the chemerin fragment or chemerin analog. 5. The method of claim 4 , wherein palmitate-PEG 8 KGG is linked at or near the N-terminus of the chemerin analog.
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