US2011142807A1PendingUtilityA1

Mesenchymal Stem Cells and Uses Therefor

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Assignee: PITTENGER MARK FPriority: Mar 22, 2004Filed: Dec 21, 2010Published: Jun 16, 2011
Est. expiryMar 22, 2024(expired)· nominal 20-yr term from priority
A61P 7/06A61P 7/04A61P 37/06A61P 35/00A61P 5/14A61P 9/00A61P 37/02A61P 3/10A61P 43/00A61P 37/08A61P 37/00A61P 29/00A61P 27/02A61P 25/00C12N 5/0667A61P 17/14C12N 5/0663C12N 5/0668A61K 38/2066A61K 2035/124A61P 17/00C12N 5/0664A61P 13/08C12N 5/0665A61P 1/00A61K 35/28A61P 19/02C12N 5/0662C12N 5/0666A61P 1/04A61P 1/02A61K 38/2026A61K 45/06A61P 11/00A61P 19/08A61P 17/02A61P 17/06A61K 35/12Y02A50/30
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Claims

Abstract

Methods of treating autoimmune diseases, allergic responses, cancer, or inflammatory diseases in an animal, promoting would healing, and promoting angiogenesis in an organ or tissue of an animal by administering to the animal mesenchymal stem cells in an effective amount.

Claims

exact text as granted — not AI-modified
1 . A method of treating an inflammatory response in an animal having inflammatory bowel disease, comprising the step of:
 administering to the animal allogeneic, isolated mesenchymal stem cells in an amount effective to treat the inflammatory response in the animal,   wherein the mesenchymal stem cells limit or reduce intestinal inflammation.   
     
     
         2 . The method of  claim 1 , wherein the animal is a human. 
     
     
         3 . The method of  claim 1 , wherein the mesenchymal stem cells are administered in an amount of from about 1×10 5  cells/kg to about 1×10 7  cells/kg. 
     
     
         4 . The method of  claim 3 , wherein the mesenchymal stem cells are administered in an amount of from about 1×10 6  cells/kg to about 5×10 6  cells/kg. 
     
     
         5 . The method of  claim 1 , wherein the mesenchymal stem cells are administered systemically. 
     
     
         6 . The method of  claim 5 , wherein the mesenchymal stem cells are administered intravenously. 
     
     
         7 . The method of  claim 5 , wherein the mesenchymal stem cells are administered intraarterially. 
     
     
         8 . The method of  claim 5 , wherein the mesenchymal stem cells are administered intraperitoneally. 
     
     
         9 . The method of  claim 1 , wherein the mesenchymal stem cells express one or more cell surface markers selected from the group consisting of CD73, CD105, and CD166. 
     
     
         10 . The method of  claim 1 , wherein the mesenchymal stem cells bind to an antibody selected from the group consisting of an antibody produced from hybridoma cell line SH2, ATCC accession number HB 10743, an antibody produced from hybridoma cell line SH3, ATCC accession number HB 10744, and an antibody produced from hybridoma cell line SH4, ATCC accession number HB 10745. 
     
     
         11 . The method of  claim 1 , wherein the mesenchymal stem cells are administered in conjunction with an acceptable pharmaceutical carrier. 
     
     
         12 . The method of  claim 11 , wherein the acceptable pharmaceutical carrier is a pharmaceutically acceptable liquid medium for injection. 
     
     
         13 . The method of  claim 1 , wherein the mesenchymal stem cells are administered as a suspension of cells. 
     
     
         14 . The method of  claim 13 , wherein at least about 95% of the cells in the suspension express one or more cell surface markers selected from the group consisting of CD73, CD105, and CD166. 
     
     
         15 . The method of  claim 13 , wherein at least about 98% of the cells in the suspension express one or more cell surface markers selected from the group consisting of CD73, CD105, and CD166. 
     
     
         16 . A method of treating intestinal inflammation associated with inflammatory bowel disease in an animal, comprising the step of:
 systemically administering to the animal a suspension of cells in an amount effective to treat the intestinal inflammation;   wherein at least about 95% of the cells are allogeneic mesenchymal stem cells.   
     
     
         17 . The method of  claim 16 , wherein the animal is a human. 
     
     
         18 . The method of  claim 16 , wherein the suspension is administered in an amount of from about 1×10 5  cells/kg to about 1×10 7  cells/kg. 
     
     
         19 . The method of  claim 16 , wherein the suspension is administered in an amount of from about 1×10 6  cells/kg to about 5×10 6  cells/kg. 
     
     
         20 . The method of  claim 16 , wherein the suspension is administered intravenously. 
     
     
         21 . The method of  claim 16 , wherein the suspension is administered intraarterially. 
     
     
         22 . The method of  claim 16 , wherein the mesenchymal stem cells express one or more cell surface markers selected from the group consisting of CD73, CD105, and CD166. 
     
     
         23 . The method of  claim 16 , wherein the mesenchymal stem cells bind to an antibody selected from the group consisting of an antibody produced from hybridoma cell line SH2, ATCC accession number HB 10743, an antibody produced from hybridoma cell line SH3, ATCC accession number HB 10744, and an antibody produced from hybridoma cell line SH4, ATCC accession number HB 10745. 
     
     
         24 . The method of  claim 16 , wherein the suspension is further comprises an acceptable pharmaceutical carrier. 
     
     
         25 . The method of  claim 24 , wherein the acceptable pharmaceutical carrier is a pharmaceutically acceptable liquid medium for injection. 
     
     
         26 . The method of  claim 16 , wherein at least about 98% of the cells in the suspension are allogeneic mesenchymal stem cells.

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