US2012020936A1PendingUtilityA1

Treatment of neurodegenerative disease using placental stem cells

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Assignee: HARIRI ROBERT JPriority: Dec 6, 2000Filed: Oct 3, 2011Published: Jan 26, 2012
Est. expiryDec 6, 2020(expired)· nominal 20-yr term from priority
A61P 7/06A61P 9/10A61P 5/14A61P 9/00A61P 43/00A61P 25/00A61P 29/00A61P 25/16A61P 25/28A61P 27/02A61P 3/00A61P 27/06A61P 17/02A61P 13/02A61P 13/12A61P 13/00A61P 21/00A61P 17/00A61P 11/00A61M 2210/1466A61M 2210/1458C12N 2509/00C12N 5/0603C12N 5/0668C12N 5/0647C12N 2510/02A61K 35/12C12M 47/04A61K 48/00A61M 1/02A61M 2202/0462A61K 2035/124A61K 35/50C12N 2533/90C12M 29/10C12N 5/0605A01N 1/122C12N 5/0607C12N 5/0606
63
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Claims

Abstract

The present invention provides a method of extracting and recovering embryonic-like stem cells, including, but not limited to pluripotent or multipotent stem cells, from an exsanguinated human placenta. A placenta is treated to remove residual umbilical cord blood by perfusing an exsanguinated placenta, preferably with an anticoagulant solution, to flush out residual cells. The residual cells and perfusion liquid from the exsanguinated placenta are collected, and the embryonic-like stem cells are separated from the residual cells and perfusion liquid. The invention also provides a method of utilizing the isolated and perfused placenta as a bioreactor in which to propagate endogenous cells, including, but not limited to, embryonic-like stem cells. The invention also provides methods for propagation of exogenous cells in a placental bioreactor and collecting the propagated exogenous cells and bioactive molecules therefrom.

Claims

exact text as granted — not AI-modified
1 - 59 . (canceled) 
     
     
         60 . A method of treating an individual who has a neurodegenerative disease, comprising administering to the individual therapeutically effective amount of isolated human placental stem cells, wherein said placental stem cells are:
 CD34 − , CD10 + , CD29 + , CD44 + , CD45 − , CD54 + , CD90 + , SH3 + , SH4 + , SSEA3 − , SSEA4 − , wherein OCT-4 is octamer binding protein 4;   OCT-4 + , CD34 − , SSEA3 −  and SSEA4 − ;   OCT-4 +  and CD34 − , and additionally SH3 +  or SH4 − ; or   CD34 −  and one or more of CD29 + , CD45 − , CD90 + , SH2 + , SH3 + , SH4 + , or MHC Class. II − .   
     
     
         61 . The method of  claim 60 , wherein said placental stem cells are CD34 − , CD10 + , CD29 + , CD44 + , CD45 − , CD54 + , CD90 + , SH3 + , SH4 + , SSEA3, SSEA4. 
     
     
         62 . The method of  claim 60 , wherein said placental stem cells are OCT-4 + , CD34 − , SSEA3 −  and SSEA4 − . 
     
     
         63 . The method of  claim 60 , wherein said placental stem cells are OCT-4 +  and CD34 − , and additionally SH3 +  or SH4 + . 
     
     
         64 . The method of  claim 63 , wherein said isolated placental stem cells have at least one of the following characteristics: CD10 + , CD29 + , CD44 + , CD45 − , CD54 + , CD90 + , SSEA3 − , or SSEA4 − . 
     
     
         65 . The method of  claim 63 , wherein said isolated placental stem cells have at least the following characteristics: CD10 + , CD29 + , CD44 + , CD45 − , CD54 − , CD90 + , SSEA3 − , and SSEA4 − . 
     
     
         66 . The method of  claim 60 , wherein said placental stem cells are CD34 −  and one or more of CD29 + , CD45 − , CD90 + , SH2 + , SH3 + , SH4 + , or MHC Class II − . 
     
     
         67 . The method of  claim 60 , wherein said neurodegenerative disease is Alzheimer's disease. 
     
     
         68 . The method of  claim 60 , wherein said neurodegenerative disease is Parkinson's disease.

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