Compositions and methods for treating fibrosis
US-10245298-B2 · Apr 2, 2019 · US
US12465640B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12465640-B2 |
| Application number | US-202017310802-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 25, 2020 |
| Priority date | Feb 25, 2019 |
| Publication date | Nov 11, 2025 |
| Grant date | Nov 11, 2025 |
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The disclosure relates to the engineering of collagen-binding modification of anti-inflammatory agents using collagen-binding peptide (CBP) and vWF A3 to achieve targeted therapy for inflammatory diseases. Accordingly, embodiments of the disclosure relate to a composition comprising an anti-inflammatory agent operatively linked to an extracellular matrix (ECM)-affinity peptide. Also disclosed are cytokines and anti-inflammatory agents, such as CD200, linked to a serum protein and/or an ECM-affinity peptide. Further aspects of the disclosure relate to a method for treating an autoimmune or inflammatory condition in a subject comprising administering a composition of the disclosure to the subject.
Opening claim text (preview).
The invention claimed is: 1 . A method for reducing inflammation in a subject comprising administering to the subject an effective amount of a composition comprising IL-10 linked to a peptide having at least 95% sequence identity to one of SEQ ID NOs: 3, 4, 5, 47, or 52. 2 . The method of claim 1 , wherein the inflammation comprises an inflammatory condition selected from the group consisting of inflammatory bowel disease, idiopathic pulmonary fibrosis, multiple sclerosis, type 1 diabetes, Crohn's disease, psoriasis, acute inflammation, chronic inflammation, neuroinflammation, and rheumatoid arthritis. 3 . The method of claim 1 , wherein the composition is administered systemically. 4 . The method of claim 3 , wherein the composition is administered by intravenous injection. 5 . The method of claim 1 , wherein the composition is administered locally. 6 . The method of claim 5 , wherein the composition is administered to or adjacent to a site of inflammation. 7 . The method of claim 1 , wherein the method further comprises administration of an additional inflammation therapy. 8 . The method of claim 1 , wherein the IL-10 linked to the peptide having 95% sequence identity to one of SEQ ID NOs: 3, 4, 5, 47, or 52 further comprises a serum protein linked to the peptide or IL-10. 9 . The method of claim 8 , wherein the serum protein comprises albumin. 10 . The method of claim 1 , wherein the ratio of peptide having 95% sequence identity to one of SEQ ID NOs: 3, 4, 5, 47, or 52 to the IL-10 is 1:1 to 5:1. 11 . The method of claim 2 , wherein the inflammatory condition comprises inflammatory bowel disease and wherein the inflammatory bowel disease is selected from Crohn's disease, autoimmune-mediated gastrointestinal diseases, colitis, and autoimmune inflammatory bowel disease. 12 . The method of claim 11 , wherein the colitis is selected from ulcerative colitis, colitis ulcerosa, microscopic colitis, collagenous colitis, colitis polyposa, necrotizing enterocolitis, and transmural colitis. 13 . The method of claim 1 , wherein the IL-10 is linked to a peptide having the amino acid sequence of one of SEQ ID NOs: 3, 4, 5, 47, or 52. 14 . The method of claim 1 , wherein the IL-10 is linked to a peptide having the amino acid sequence of SEQ ID NO:47. 15 . The method of claim 1 , wherein the IL-10 is linked to a peptide having the amino acid sequence of SEQ ID NO:52.
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