US2014107035A1PendingUtilityA1

Methods of treating fibrosing diseases by induction of immune tolerance

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Assignee: UNIV TENNESSEE RES FOUNDATIONPriority: Nov 16, 2005Filed: Dec 13, 2013Published: Apr 17, 2014
Est. expiryNov 16, 2025(expired)· nominal 20-yr term from priority
A61P 9/00A61P 43/00A61P 17/00A61P 13/12A61K 38/39A61P 1/00A61P 11/00A61P 1/16A61K 38/16A61K 38/00
55
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Claims

Abstract

The present invention has demonstrated for the first time that orally administered type I collagen (CI) induced tolerance to CI in patients suffering from systemic sclerosis (SSc) and ameliorated clinical manifestations of the disease. Accordingly, the present invention provides methods of treating a fibrosing disease by oral administration of a tissue protein, for example, collagen, derived from the tissue undergoing fibrosis.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for treating a fibrosing disease in a patient, comprising orally administering to the patient one or more collagen fragments, said collagen fragments selected from the group consisting of: α1(I) CB1, CB2, CB3, CB4, CB5, CB6, CB7, CB8 and α2(I) CB1, CB2, CB3, CB4 and CB5. 
     
     
         2 . The method of  claim 1 , wherein said fibrosing disease is selected from the group consisting of skin fibrosis, liver cirrhosis, renal fibrosis, lung fibrosis, heart fibrosis, gastrointestinal fibrosis and vascular fibrosis. 
     
     
         3 . The method of  claim 1 , wherein said patient has been suffering from said fibrosing disease for at least 3 years. 
     
     
         4 . The method of  claim 1 , wherein said collagen is derived from human or an animal species other than human. 
     
     
         5 . The method of  claim 1 , wherein said collagen is orally administered to said patient at about 500 μg/day. 
     
     
         6 . The method of  claim 1 , wherein the patient is treated for about 12 months. 
     
     
         7 . The method of  claim 1 , wherein the patient is treated for about 36 months. 
     
     
         8 . The method of  claim 1 , wherein the oral administration of said collagen induces tolerance in said patient. 
     
     
         9 . A dosage form for oral administration for treating a fibrosing disease in a patient, comprising one or more collagen fragments, said collagen fragments selected from the group consisting of: α(I) CB2, CB3, CB4, CB5, CB6, CB7, CB8, and α2(I) CB0, CB1, CB2, CB3, CB4 and CB5. 
     
     
         10 . The dosage form of  claim 9 , wherein said dosage form is adapted for daily administration. 
     
     
         11 . The dosage form of  claim 9 , wherein said one or more collagen fragments is adapted to induced tolerance in said patient upon oral administration. 
     
     
         12 . The dosage form of  claim 9 , wherein said dosage form is orally administered to a patient at about 500 μg/day.

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