US2021213068A1PendingUtilityA1

Pluripotent stem cell for treatment of cerebral infarction

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Assignee: LIFE SCIENCE INST INCPriority: Feb 25, 2014Filed: Mar 31, 2021Published: Jul 15, 2021
Est. expiryFeb 25, 2034(~7.6 yrs left)· nominal 20-yr term from priority
A61P 9/10A61K 35/545A61P 25/28A61K 35/28A61P 25/00A61P 43/00A61P 9/00
61
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Claims

Abstract

An object of the present invention is to provide a novel medical application to regenerative medicine that uses pluripotent stem cells (Muse cells). The present invention provides a cell preparation for treating cerebral infarction and sequelae associated therewith that contains SSEA-3-positive pluripotent stem cells isolated from mesenchymal tissue in the body or cultured mesenchymal cells. The cell preparation of the present invention is based on a brain tissue regeneration mechanism by which Muse cells differentiate into nerve cells and the like in damaged brain tissue by administering Muse cells into cerebral parenchyma.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for treating a cerebral infarction in a subject in need thereof, the method comprising: administering a cell preparation containing pluripotent stem cells positive for SSEA-3 isolated from biological mesenchymal tissue or cultured mesenchymal cells to the subject, to treat the cerebral infarction. 
     
     
         2 . The method according to  claim 1 , wherein the cell preparation prevents and/or treats sequelae from cerebral infarction. 
     
     
         3 . The method according to  claim 1 , wherein the pluripotent stem cells positive for SSEA-3 contain a concentrated cell fraction as a result of stimulation by external stress. 
     
     
         4 . The method according to  claim 1 , wherein the pluripotent stem cells are CD105-positive. 
     
     
         5 . The method according to  claim 1 , wherein the pluripotent stem cells are CD117-negative and CD146-negative. 
     
     
         6 . The method according to  claim 1 , wherein the pluripotent stem cells are CD117-negative, CD146-negative, NG2-negative, CD34-negative, vWF-negative and CD271-negative. 
     
     
         7 . The method according to  claim 1 , wherein the pluripotent stem cells are CD34-negative, CD117-negative, CD146-negative, CD271-negative, NG2-negative, vWF-negative, Sox10-negative, Snail-negative, Slug-negative, Tyrp1-negative and Dct-negative. 
     
     
         8 . The method according to  claim 1 , wherein the pluripotent stem cells are pluripotent stem cells having all of the properties indicated below:
 (i) low or absent telomerase activity;   (ii) ability to differentiate into any of the three germ layers;   (iii) absence of demonstration of neoplastic proliferation; and,   iv) self-renewal ability.   
     
     
         9 . The method according to  claim 1 , wherein the pluripotent stem cells have the ability to differentiate into one or more cells selected from the group consisting of nerve cells, glial cells, vascular endothelial cells, and/or microglial cells. 
     
     
         10 . The method according to  claim 1 , wherein the pluripotent stem cells reduce infarct size by a mechanism involving regeneration of brain tissue.

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