IP Library Granted Patent US 10,501,725
Granted Patent B2
US 10,501,725 · App. 15/535,032 · Granted Dec 10, 2019

Method for producing therapeutic corneal endothelial substitute cell sphere

Inventors: Shigeto Shimmura (Tokyo, JP); Shin Hatou (Tokyo, JP); Kazuo Tsubota (Tokyo, JP)
Assignee: KEIO UNIVERSITY
C12N5/0621A61K31/203A61K35/30A61K35/44A61K38/22A61K38/28A61K47/36A61K48/0091A61P27/02C12N5/10A61F9/0017
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,501,725
App. No.
15/535,032
Granted
Dec 10, 2019
Kind
B2
Abstract

The problem of the present invention is to provide a method of efficiently producing therapeutic alternative corneal endothelial cells, particularly, a method capable of stably producing them in a condition suitable for intraocular transplantation (in the anterior chamber) in a large amount. Furthermore, the present invention aims to provide a composition for transplantation, which is preferable for intraocular administration, particularly, into the anterior chamber. A therapeutic alternative corneal endothelial cell sphere can be produced by culturing stem cells in suspension in a differentiation induction medium containing a GSK3 inhibitor, retinoic acid and a ROCK inhibitor. Addition of a viscoelastic substance during intraocular (into the anterior chamber) transplantation of the sphere or cultured corneal endothelial cells dispersed into single cells can increase the number of adherent cells after transplantation.

Claims (11)

1. A pharmaceutical composition for transplantation comprising a therapeutic corneal endothelial cell sphere suspension having a cell density of 1-5×10 6 cells/ml, and a viscoelastic substance, wherein the viscoelastic substance is 5-40 mg/ml hyaluronic acid and/or 5-50 mg/ml chondroitin sulfate, and wherein the ratio of viscoelastic substance:cell sphere suspension is 1:1 to 1:5.

2. A pharmaceutical composition for transplantation comprising a cultured corneal endothelial cell suspension having a cell density of 1-5 ×10 6 cells/ml, and a viscoelastic substance, wherein the cultured corneal endothelial cells are dispersed as single cells or in the form of a cell aggregate, wherein the viscoelastic substance is 5-40 mg/ml hyaluronic acid and/or 5-50 mg/ml chondroitin sulfate, and wherein the ratio of viscoelastic substance:cell suspension is 1:1 to 1:5.

3. The pharmaceutical composition according to claim 1 , which is for transplantation into anterior chamber.

4. The pharmaceutical composition according to claim 1 , wherein the sphere of therapeutic corneal endothelial cells is obtained by a production method comprising culturing stem cells in suspension in a differentiation induction medium, wherein the differentiation induction medium comprises a GSK3inhibitor, retinoic acid and a ROCK inhibitor.

5. The pharmaceutical composition according to claim 2 , wherein the cultured corneal endothelial cells in the suspension are dispersed into single cells.

6. The pharmaceutical composition according to claim 1 , further comprising retinoic acid and a ROCK inhibitor.

7. The pharmaceutical composition according to claim 6 , further comprising insulin, EGF and bFGF.

8. The pharmaceutical composition according to claim 2 , which is for transplantation into anterior chamber.

9. The pharmaceutical composition according to claim 2 , further comprising retinoic acid and a ROCK inhibitor.

10. The pharmaceutical composition according to claim 9 , further comprising insulin, EGF and bFGF.

11. A method for improving cell engraftment during transplantation, comprising transplanting a corneal endothelial cell composition comprising (a) a cultured corneal endothelial cell suspension having a cell density of 1-5×10 6 cells/ml and (b) a viscoelastic substance into an anterior chamber of an eye, wherein the viscoelastic substance is 5-40 mg/ml hyaluronic acid and/or 5-50 mg/ml chondroitin sulfate, wherein the cells are dispersed into single cells or used in the form of a cell aggregate, wherein the ratio of viscoelastic substance:cell suspension is 1:1 to 1:5.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2017
From: SHIMMURA, SHIGETO; HATOU, SHIN; TSUBOTA, KAZUO
To: KEIO UNIVERSITY
Reel/Frame 042670/0663 →
Priority Claims (1)
JP 2014-251236 · Dec 11, 2014 · national
Continuity (1)
Related Publication 20170340677A1 · Nov 30, 2017
Cited By (1)
US 12,350,294