US2018071343A1PendingUtilityA1

Angiogenesis using placental stem cells

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Assignee: ABBOT STEWARTPriority: Apr 7, 2010Filed: Nov 16, 2017Published: Mar 15, 2018
Est. expiryApr 7, 2030(~3.7 yrs left)· nominal 20-yr term from priority
A61P 7/02A61P 35/00A61P 9/12A61P 9/10A61P 9/04A61P 9/00A61P 9/06A61P 29/00A61L 27/3834A61L 27/3895A61L 27/3633C12N 5/0605A61K 35/50A61L 27/3683A61K 35/28A61L 27/3808A61L 27/3886A61K 9/0019A61K 9/0085A61L 27/3604A61K 2300/00A61P 25/02
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Claims

Abstract

Provided herein are methods of treating individuals having diseases or disorders of the circulatory system, using placental cells, e.g., the placental stem cells and placental multipotent cells (PDACs) described herein, and populations of such placental cells. The invention also provides methods of angiogenesis using such cells or populations of cells comprising such cells.

Claims

exact text as granted — not AI-modified
What is claimed: 
     
         1 . An isolated placental derived adherent cell, wherein said cell is adherent to tissue culture plastic, and wherein said cell is CD10 + , CD34 − , CD105 +  and CD200 +  as determined by flow cytometry, and wherein said cell (1) promotes the proliferation of endothelial cells; (2) promotes the formation of sprouts or tube-like structures in a population of endothelial cells; or (3) promote the migration of endothelial cells. 
     
     
         2 . The isolated cell of  claim 1 , wherein said cell is CD45 −  and CD90 + , as determined by flow cytometry. 
     
     
         3 . The isolated cell of  claim 1 , wherein said cells express one or more of VEGF, HGF, IL-8, MCP-3, FGF2, follistatin, G-CSF, EGF, ENA-78, GRO, IL-6, MCP-1, PDGF-BB, TIMP-2, uPAR, or galectin-1 as determined by antibody binding. 
     
     
         4 . An isolated population of cells comprising the cell of  claim 1 . 
     
     
         5 . The isolated population of cells of  claim 4 , wherein at least 50% of the cells in said population are the cells of  claim 1 . 
     
     
         6 . The isolated population of cells of  claim 4 , wherein at least 90% of the cells in said population are the cells of  claim 1 . 
     
     
         7 . The isolated population of cells of  claim 7 , wherein at least 50% of the cells in said population are the cells of  claim 1 . 
     
     
         8 . The isolated population of cells of  claim 1 , wherein at least 90% of the cells in said population are the cells of  claim 1 . 
     
     
         9 . A composition comprising the isolated placental derived adherent cell of  claim 1 . 
     
     
         10 . The isolated population of  claim 4  comprising a second type of cell. 
     
     
         11 . The isolated population of cells of  claim 10 , wherein said second type of cell is an embryonic stem cell, a blood cell, a stem cell isolated from peripheral blood, a stem cell isolated from placental blood, a stem cell isolated from umbilical cord blood, an umbilical cord stem cell, a bone marrow-derived mesenchymal stem cell, a bone marrow-derived mesenchymal stromal cell, a hematopoietic stem cell, a somatic stem cell, a chondrocyte, a fibroblast, a muscle cells, an endothelial cell, an angioblast, an endothelial progenitor cell, a pericyte, a cardiomyocyte, a myocyte, a cardiomyoblast, a myoblast, an embryonic stem cell, or a cell manipulated to resemble an embryonic stem cell. 
     
     
         12 . The isolated population of cells of  claim 11 , wherein said second type of cell comprises at least 10% of cells in said population. 
     
     
         13 . The isolated population of cells of  claim 11 , wherein said second type of cell comprises at least 25% of cells in said population. 
     
     
         14 . The isolated population of cells of  claim 11 , wherein said second type of cell is a hematopoietic stem or progenitor cell. 
     
     
         15 . The isolated population of  claim 14 , wherein said hematopoietic stem or progenitor cell is a CD34 +  cell. 
     
     
         16 . A permanent or degradable decellularized or synthetic matrix or scaffold comprising the cell of  claim 1 . 
     
     
         17 . The matrix or scaffold of  claim 16 , wherein said matrix or scaffold is an amniotic membrane; a dehydrated extracellular matrix; placental collagen, or placental extracellular membrane. 
     
     
         18 . A method of treating an individual having a disease or disorder of the circulatory system, comprising administering a population of the cells of  claim 1  to said individual in an amount and for a time sufficient for detectable improvement of one or more symptoms of said disease or disorder. 
     
     
         19 . A method of treating an individual having a disease or disorder of the circulatory system, comprising administering a population of the cells of  claim 1  to said individual in an amount and for a time sufficient for detectable improvement of one or more indicia of cardiac function, wherein said indicia of cardiac function are chest cardiac output (CO), cardiac index (CI), pulmonary artery wedge pressure (PAWP), cardiac index (CI), % fractional shortening (% FS), ejection fraction (EF), left ventricular ejection fraction (LVEF); left ventricular end diastolic diameter (LVEDD), left ventricular end systolic diameter (LVESD), contractility (dP/dt), a decrease in atrial or ventricular functioning, an increase in pumping efficiency, a decrease in the rate of loss of pumping efficiency, a decrease in loss of hemodynamic functioning, or decrease in complications associated with cardiomyopathy, as compared to the individual prior to administration of placental derived adherent cells. 
     
     
         20 . A method of treating an individual having a disruption of blood flow in or around a limb, comprising administering a therapeutically effective amount of the placental derived adherent cells of  claim 1 .

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