US2017319623A1PendingUtilityA1

Multipotent stem cells and uses thereof

Assignee: BRIGHAM & WOMENS HOSPITAL INCPriority: May 3, 2007Filed: Dec 19, 2016Published: Nov 9, 2017
Est. expiryMay 3, 2027(~0.8 yrs left)· nominal 20-yr term from priority
A61P 37/02A61P 9/00A61P 17/02C12N 2501/39C12N 2501/2303C12N 5/0676C12N 5/0662C12N 2500/25C12N 2500/38C12N 2500/36C12N 2501/999C12N 2501/2306C12N 5/0657C12N 2501/41A61K 35/12C12N 2501/235C12N 2501/135C12N 5/0661C12N 5/067C12N 5/0658C12N 2501/105C12N 2501/11C12N 2501/26C12N 5/0653C12N 2501/40C12N 5/0668C12N 2501/125C12N 2501/22A61K 35/14C12N 5/0654C12N 2501/155C12N 5/0655C12N 5/0647A61K 35/24C12N 5/0639
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Claims

Abstract

The invention provides a quiescent stem cell having the capacity to differentiate into ectoderm, mesoderm and endoderm, and which does not express cell surface markers including MHC class I, MHC class II, CD44, CD45, CD13, CD34, CD49c, CD73, CD105 and CD90. The invention further provides a proliferative stem cell, which expresses genes including Oct-4, Nanog, Sox2, GDF3, P16INK4, BMI, Notch, HDAC4, TERT, Rex-1 and TWIST but does not express cell surface markers including MHC class I, MHC class II, CD44, CD45, CD13, CD34, CD49c, CD73, CD105 and CD90. The cells of the invention can be isolated from adult mammals, have embryonic cell characteristics, and can form embryoid bodies. Methods for obtaining the stem cells, as well as methods of treating diseases and the differentiated stem cells, are also provided.

Claims

exact text as granted — not AI-modified
1 . A tissue regenerative formulation comprising:
 a population of stem cells that express a stem cell transcription factor but do not detectably express MHC Class I or cell surface markers CD13, CD44, CD45, CD90, and CD105;   and a pharmaceutically acceptable carrier.   
     
     
         2 . The formulation of  claim 1 , further comprising a cellular differentiating agent. 
     
     
         3 . The formulation of  claim 2 , wherein the cellular differentiating agent is a chondrogenic agent. 
     
     
         4 . The formulation of  claim 3 , wherein the chondrogenic agent is a corticosteroid, a cytokine or a growth factor. 
     
     
         5 . The formulation of  claim 4 , wherein the chondrogenic agent is selected from the group consisting of: dexamethasone, TGF-beta and BMPs. 
     
     
         6 . The formulation of  claim 2 , wherein the cellular differentiating agent is a tenocyte inducing agent. 
     
     
         7 . The formulation of  claim 6 , wherein the tenocyte inducing agent is a BMP. 
     
     
         8 . The formulation of  claim 2 , wherein the cellular differentiating agent is an osteoinductive agent. 
     
     
         9 . The formulation of  claim 8 , wherein the cellular osteoinductive agent is a BMP. 
     
     
         10 . The formulation of  claim 2 , wherein the cellular differentiating agent is an endothelial cell-inductive agent. 
     
     
         11 . The formulation of  claim 10 , wherein the endothelial cell-inductive agent is a growth factor. 
     
     
         12 . The formulation of  claim 2 , wherein the population of stem cells is committed to differentiate. 
     
     
         13 . The formulation of  claim 1 , further comprising at least one subpopulation of differentiated progeny cells. 
     
     
         14 . The formulation of  claim 1 , further comprising at least one subpopulation of differentiated immune cells. 
     
     
         15 . The formulation of  claim 1 , further comprising an extracellular matrix component. 
     
     
         16 . The formulation of  claim 1 , wherein the population of stem cells further comprise a subpopulation of stem cells having a transgene that expresses a polypeptide or oligonucleotide. 
     
     
         17 . The formulation of  claim 1 , wherein the population of stem cells is autologous with respect to an intended recipient of the formulation. 
     
     
         18 . The formulation of  claim 1 , wherein the population of stem cells is allogeneic with respect to an intended recipient of the formulation.

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