IP Library Granted Patent US 8,529,888
Granted Patent B2
US 8,529,888 · App. 12/678,756 · Granted Sep 10, 2013

Adherent cells from adipose or placenta tissues and use thereof in therapy

Inventors: Moran Meiron (Zikhron-Yaakov, IL); Amir Toren (Zikhron-Yaakov, IL); Rachel Ofir (Mitzpe Adi, IL); Zami Aberman (Tel-Mond, IL); Nirit Drori-Carmi (Kibbutz Nahsholim - Doar-Na Hof HaCarmel, IL)
Assignee: Pluristem Ltd.
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Quick Facts
Patent No.
US 8,529,888
App. No.
12/678,756
Granted
Sep 10, 2013
Kind
B2
Abstract

A method of treating ischemia in a subject in need thereof is disclosed. The method comprising administering to the subject a therapeutically effective amount of adherent cells of a tissue selected from the group consisting of a placenta and an adipose tissue, thereby treating the ischemia in the subject. A method of treating a medical condition requiring connective tissue regeneration and/or repair is also disclosed.

Claims (18)

1. A method of treating ischemia peripheral arterial disease (PAD) in a subject in need of treatment for PAD, comprising:

administering to the subject a therapeutically effective amount of undifferentiated placenta-derived adherent stromal cells,

wherein the adherent stromal cells do not express CD34;

thereby treating the PAD.

2. The method of claim 1 , wherein at least 10% of said cells are at a proliferative phase.

3. The method of claim 1 , wherein said peripheral arterial disease (PAD) is critical limb ischemia (CLI).

4. The method of claim 1 , wherein said cells are propagated in three-dimensional (3D) culturing conditions.

5. The method of claim 4 , wherein said three-dimensional (3D) culturing conditions comprise a 3D bioreactor.

6. The method of claim 4 , wherein said three-dimensional (3D) culturing conditions are effected under perfusion.

7. The method of claim 4 , wherein said three-dimensional (3D) culturing conditions comprise an adherent material selected from the group consisting of a polystyrene, a polyester, and a polypropylene.

8. The method of claim 1 , wherein culturing of said cells is effected for at least 3 days.

9. The method of claim 1 , wherein culturing of said cells is effected until at least 10% of said cells are proliferating.

10. The method of claim 4 , wherein said cells express a marker selected from the group consisting of CD73, CD90, CD29 and CD105.

11. The method of claim 4 , wherein said cells do not express a marker selected from the group consisting of CD3, CD4, CD45, CD80, HLA-DR, CD11b, CD14, CD19, and CD79.

12. The method of claim 6 , wherein said perfusion rate is adjusted in order to maintain a constant glucose concentration in the culture medium.

13. The method of claim 12 , wherein said constant glucose concentration is about 550 mg/L.

14. The method of claim 1 , wherein said cells are propagated in two-dimensional (2D) culturing conditions.

15. The method of claim 14 , wherein said cells express a marker selected from the group consisting of CD90, CD105, CD73 and CD29.

Assignments (2)
CHANGE OF NAME Recorded Dec 30, 2022
From: PLURISTEM LTD.
To: PLURI BIOTECH LTD.
Reel/Frame 062247/0037 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2010
From: MEIRON, MORAN; TOREN, AMIR; OFIR, RACHEL; ABERMAN, ZAMI; DRORI-CARMI, NIRIT
To: PLURISTEM LTD.
Reel/Frame 024148/0977 →
Continuity (2)
Provisional Application 60960184 · Sep 19, 2007
Related Publication 20100209403A1 · Aug 19, 2010