IP Library › Granted Patent US 10,058,572
Granted Patent B2
US 10,058,572 · App. 14/912,066 · Granted Aug 28, 2018

Placenta-derived multipotent stem cells

Inventors: Aijun Wang (Davis, CA); Diana L. Farmer (Davis, CA)
Assignee: The Regents of the University of California
A61K35/28A61K35/50C12N5/0605C12N5/0668A61K9/0085A61K9/06
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Quick Facts
Patent No.
US 10,058,572
App. No.
14/912,066
Granted
Aug 28, 2018
Kind
B2
Abstract

This disclosure provides isolated cells and compositions comprising one or more isolated cell(s) as described herein. In one aspect, the isolated cell is a pre-term placenta-derived stem cell (also referred to placenta-derived multi potent stem cells (pmSCs). As used herein, the term “pre-term placenta-derived multipotent stem cell or placenta-derived stem cells” intends a cell isolated from placental tissue prior to delivery of the fetus by surgery or birth. In another aspect, the isolated cell is a chorionic villus (CV)-derived multipotent placental stem cells (C-mpSCs). Also provided are compositions comprising these cells, wherein the composition comprises an effective amount of the isolated cells as described herein.

Claims (13)

1. A method for treating spina bifida in a subject in need thereof comprising administering to the subject an effective amount of an isolated pre-term placenta-derived multipotent stem cell or cells (PMSCs) or culture conditioned media therefrom.

2. The method of claim 1 , wherein the PMSCs comprise chorionic villus (CV)-derived multipotent stem cells (C-mpSCs).

3. The method of claim 1 , wherein the PMSCs or the culture conditioned media therefrom are administered in a pharmaceutically acceptable carrier or a biocompatible matrix.

4. The method of claim 1 or 3 , wherein the subject is a fetus and the PMSCs or the culture conditioned media therefrom is administered to the fetus in utero.

5. The method of claim 1 , wherein said PMSCs express one or both markers of CD56 + or CD271 + .

6. The method of claim 5 , wherein said PMSCs express one or more markers of CD105 + , CD90 + , CD73 + , CD44 + or CD29 + .

7. The method of claim 5 , wherein said PMSCs express the marker CD184 + .

8. The method of claim 1 , wherein said PMSCs express an integrin receptor comprising one or both of CD49d or CD49f.

9. The method of claim 1 , wherein said PMSCs express an intracellular marker comprising one or more of Nestin, Vimentin, S100β or neurofilament medium (NFM).

10. The method of claim 1 , wherein said PMSCs express a transcriptional factor comprising one or more of Sox2, Sox10, Sox17 or Slug.

11. The method of claim 1 , wherein said PMSCs lack expression of one or more endothelial markers or hematopoietic markers.

12. The method of claim 11 , wherein said marker is one or more of CD31, CD34 or CD45.

13. The method of claim 1 , wherein the conditioned media is concentrated in an amount selected from the group of at least about 5 fold; at least about 10 fold; at least about 15 fold; at least about 20 fold; at least about 25 fold; at least about 30 fold; at least about 35 fold; at least about 40 fold; at least about 45 fold; at least about 50 fold; at least about 55 fold; at least about 60 fold; at least about 65 fold; at least about 70 fold; at least about 75 fold; at least about 80 fold; at least about 85 fold; or at least about 90 fold.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 22, 2018
From: WANG, AIJUN; FARMER, DIANA L.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 045869/0942 →
Continuity (3)
Provisional Application 61866524 · Aug 15, 2013
Provisional Application 61982804 · Apr 22, 2014
Related Publication 20160184365A1 · Jun 30, 2016