US2004091464A1PendingUtilityA1

Isolated stromal cells for use in the treatment of diseases of the central nervous system

Assignee: PHILADELPHIA HEALTH & EDUCATIOPriority: Mar 28, 1995Filed: Jun 27, 2003Published: May 13, 2004
Est. expiryMar 28, 2015(expired)· nominal 20-yr term from priority
A61P 35/00A61P 43/00A61P 25/16A61P 25/00A61P 25/28A61K 48/00C12N 2502/1311C12N 2501/135C12N 2502/08A61K 35/28A61K 38/44A61K 38/177C12Y 114/16002C12N 5/0622C12N 2799/027A61K 38/4846C07K 14/4702A61P 11/00A61K 38/2264C07K 14/78C07K 16/2845A61K 38/00C12Y 304/21022C12N 5/0663C07K 14/745C12N 2506/1353C07K 14/61
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Claims

Abstract

Methods of treating a human patient having a disease, disorder or condition of the central nervous system are disclosed. The methods include obtaining a bone marrow sample from a human donor, isolating stromal cells from the bone marrow sample, and administering the isolated stromal cells to the central nervous system of the human patient, wherein the presence of the isolated stromal cells in the brain effects treatment of the disease, disorder or condition. Stromal cells which are isolated may be cultured in vitro, they may be genetically engineered to produce therapeutic compounds, and/or they may be pre-differentiated prior to administration into the central nervous system.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A method of treating a human patient having a disease, disorder or condition of the central nervous system, the method comprising obtaining a bone marrow sample from a human donor, isolating stromal cells from said bone marrow sample, and administering said isolated stromal cells to the central nervous system of said human patient, wherein the presence of said isolated stromal cells in said central nervous system effects treatment of said disease, disorder or condition.  
     
     
         2 . The method of  claim 1 , wherein said human donor is not suffering from a disease, disorder or condition of the central nervous system and wherein said human donor is synergeneic with said patient.  
     
     
         3 . The method of  claim 1 , wherein said human donor is said human patient.  
     
     
         4 . The method of  claim 1 , wherein said disease, disorder or condition of the central nervous system is selected from the group consisting of a genetic disease, a tumor, trauma and stroke.  
     
     
         5 . The method of  claim 4 , wherein said disease, disorder or condition is injury to the tissues or cells of said central nervous system.  
     
     
         6 . The method of  claim 4 , wherein said disease, disorder or condition is a brain tumor.  
     
     
         7 . The method of  claim 1 , wherein said isolated stromal cells administered to said central nervous system remain present or replicate in said central nervous system.  
     
     
         8 . The method of  claim 1 , wherein prior to administering said isolated stromal cells, said cells are cultured in vitro.  
     
     
         9 . The method of  claim 1 , wherein prior to administering said isolated stromal cells, said isolated stromal cells are transfected with an isolated nucleic acid encoding a therapeutic protein, wherein when said protein is expressed in said cells said protein serves to effect treatment of said disease, disorder or condition.  
     
     
         10 . The method of  claim 9 , wherein said therapeutic protein is selected from the group consisting of a cytokine, a chemokine and a neurotrophin.  
     
     
         11 . The method of  claim 1 , wherein prior to administering said isolated stromal cells, said isolated stromal cells are transfected with an isolated nucleic acid encoding a therapeutic protein wherein when such protein is secreted by said cells said protein serves to effect treatment of said disease, disorder or condition.  
     
     
         12 . The method of  claim 11 , wherein said isolated nucleic acid is operably linked to a promoter/regulatory sequence.  
     
     
         13 . The method of  claim 11 , wherein said therapeutic protein is selected from the group consisting of a cytokine, a chemokine and a neurotrophin.  
     
     
         14 . The method of  claim 9 , wherein said isolated nucleic acid is a wild type copy of a mutated, non-functioning or under-expressed gene, wherein said isolated nucleic acid is operably linked to a promoter/regulatory sequence and is expressed in said isolated stromal cells.  
     
     
         15 . The method of  claim 11 , wherein said isolated nucleic acid is a wild type copy of a mutated, non-functioning or under-expressed gene, wherein said isolated nucleic acid is operably linked to a promoter/regulatory sequence and is expressed in to generate a protein which is secreted from said isolated stromal cells.  
     
     
         16 . The method of  claim 1 , wherein prior to administrating said stromal cells, said cells are pre-differentiated by coculturing said stromal cells in the presence of a substantially homogeneous population of differentiated cells, whereby said stromal cells differentiate and acquire the phenotypic characteristics of said differentiated cells.  
     
     
         17 . The method of  claim 1 , wherein prior to administration of said isolated stromal cells at least one of the steps of culturing said cells in vitro, introducing isolated nucleic acid into said cells, and pre-differentiating said cells, is performed.  
     
     
         18 . The method of  claim 1 , wherein said isolated stromal cells are immunologically isolated.  
     
     
         19 . A method of directing the differentiation of an isolated stromal cell comprising culturing said isolated stromal cell in the presence of a substantially homogeneous population of differentiated cells whereby said isolated stromal cell differentiates and acquires the phenotypic characteristics of said differentiated cells.  
     
     
         20 . The method of  claim 19 , wherein said differentiated cells are astrocytes.

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