US2006216276A1PendingUtilityA1

Use of materials for treatment of central nervous system lesions

Assignee: DEZAWA MARIPriority: Mar 7, 2005Filed: Mar 6, 2006Published: Sep 28, 2006
Est. expiryMar 7, 2025(expired)· nominal 20-yr term from priority
A61P 9/10A61K 35/30A61P 25/00
50
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

Disclosed are methods and materials for treatment of central nervous system lesions. Preferred methods and materials comprise neuronal precursor cells and/or marrow adherent stem cell-derived neuronal cells.

Claims

exact text as granted — not AI-modified
1 . A method comprising: 
 providing neuronal precursor cells; and    administering the neuronal precursor cells to a patient suffering from a central nervous system lesion in an amount sufficient to facilitate functional recovery of the patient.    
     
     
         2 . The method of  claim 1 , wherein the neuronal precursor cells are administered locally.  
     
     
         3 . The method of  claim 2 , wherein the neuronal precursor cells are administered to a central nervous system lesion of the patient.  
     
     
         4 . The method of  claim 1 , wherein the neuronal precursor cells are administered intraparenchymally.  
     
     
         5 . The method of  claim 1 , wherein the neuronal precursor cells comprise human neuronal precursor cells.  
     
     
         6 . The method of  claim 1 , wherein providing neuronal precursor cells comprises: 
 providing marrow adherent stem cells;    transdifferentiating the marrow adherent stem cells into neuronal precursor cells.    
     
     
         7 . The method of  claim 1 , wherein the central nervous system lesion is caused by ischemic stroke or hemorrhagic stroke.  
     
     
         8 . The method of  claim 1 , further comprising 
 allowing the neuronal precursor cells to migrate from a site of administration to other locations in the patient.    
     
     
         9 . The method of  claim 8 , wherein another location in the patient comprises a central nervous system lesion.  
     
     
         10 . The method of  claim 1 , further comprising 
 administering an immunosuppressive agent to the patient.    
     
     
         11 . The method of  claim 1 , wherein the functional recovery is a partial functional recovery.  
     
     
         12 . The method of  claim 1 , wherein the neuronal precursor cells are allogeneic with respect to the patient.  
     
     
         13 . A graft forming unit comprising: 
 neuronal precursor cells present in an amount sufficient to facilitate functional recovery of a patient suffering from a central nervous system lesion following administration of the neuronal precursor cells to the patient; and    a pharmaceutically acceptable carrier.    
     
     
         14 . The graft forming unit of  claim 13 , wherein the pharmaceutically acceptable carrier comprises a solvent, a dispersion media, an antibacterial agents, or an antifungal agent.  
     
     
         15 . The graft forming unit of  claim 13 , wherein the graft comprises neuronal precursor cells in an amount ranging from about 10,000 to about 100 million neuronal precursor cells.  
     
     
         16 . The graft forming unit of  claim 13 , wherein the neuronal precursor cells comprise a label.  
     
     
         17 . The graft forming unit of  claim 13 , wherein the neuronal precursor cells comprise human neuronal precursor cells.  
     
     
         18 . A method comprising: 
 providing marrow-adherent stem cell-derived neuronal cells; and    administering the marrow-adherent stem cell-derived neuronal cells to a patient suffering from a central nervous system lesion in an amount sufficient to facilitate functional recovery of the patient.    
     
     
         19 . The method of  claim 18 , wherein the marrow-adherent stem cell-derived neuronal cells are administered locally.  
     
     
         20 . The method of  claim 19 , wherein the marrow-adherent stem cell-derived neuronal cells are administered to a central nervous system lesion of the patient.  
     
     
         21 . The method of  claim 18 , wherein the marrow-adherent stem cell-derived neuronal cells are administered intraparenchymally.  
     
     
         22 . The method of  claim 18 , wherein the marrow-adherent stem cell-derived neuronal cells comprise human marrow-adherent stem cell-derived neuronal cells.  
     
     
         23 . The method of  claim 18 , wherein providing marrow-adherent stem cell-derived neuronal cells comprises: 
 providing marrow adherent stem cells; and    inducing the marrow adherent stem cells to form marrow-adherent stem cell-derived neuronal cells.    
     
     
         24 . The method of  claim 23 , further comprising: 
 transdifferentiating the marrow adherent stem cells into neuronal precursor cells; and    inducing the neuronal precursor cells to form neuronal cells.    
     
     
         25 . The method of  claim 18 , wherein the central nervous system lesion is caused by ischemic stroke or hemorrhagic stroke.  
     
     
         26 . The method of  claim 18 , further comprising administering an immunosuppressive agent to the patient.  
     
     
         27 . The method of  claim 18 , wherein the functional recovery is a partial functional recovery.  
     
     
         28 . The method of  claim 18 , wherein the marrow-adherent stem cell-derived neuronal cells are allogeneic with respect to the patient.  
     
     
         29 . A graft forming unit comprising: 
 marrow-adherent stem cell-derived neuronal cells present in an amount sufficient to facilitate functional recovery of a patient suffering from a central nervous system lesion following administration of the marrow-adherent stem cell-derived neuronal cells to the patient; and    a pharmaceutically acceptable carrier.    
     
     
         30 . The graft forming unit of  claim 29 , wherein the pharmaceutically acceptable carrier comprises a solvent, a dispersion media, an antibacterial agents, or an antifungal agent.  
     
     
         31 . The graft forming unit of  claim 29 , wherein the graft comprises neuronal precursor cells in an amount ranging from about 10,000 to about 100 million neuronal precursor cells.  
     
     
         32 . The graft forming unit of  claim 29 , wherein the marrow-adherent stem cell-derived neuronal cells comprise a label.  
     
     
         33 . The graft forming unit of  claim 29 , wherein the marrow-adherent stem cell-derived neuronal cells comprise human marrow-adherent stem cell-derived neuronal cells.

Join the waitlist — get patent alerts

Track US2006216276A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.