IP Library Granted Patent US 12,083,149
Granted Patent B2
US 12,083,149 · App. 16/322,781 · Granted Sep 10, 2024

Amelioration and treatment of chronic lung disease using pluripotent stem cells

Inventors: Yoshiaki Sato (Nagoya, JP); Toshihiko Suzuki (Nagoya, JP); Shinobu Shimizu (Nagoya, JP); Masaaki Mizuno (Nagoya, JP); Masahiro Hayakawa (Nagoya, JP); Mari Dezawa (Sendai, JP)
Assignee: TOHOKU UNIVERSITY
A61K35/545A61P11/00
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Quick Facts
Patent No.
US 12,083,149
App. No.
16/322,781
Granted
Sep 10, 2024
Kind
B2
Abstract

The purpose of the present invention is to provide a novel medical use of pluripotent stem cells (Muse cells) in the regenerative medicine area. Provided are a cell preparation and a medicinal composition for ameliorating and treating chronic lung disease in newborns, said cell preparation and medicinal composition comprising SSEA-3-positive pluripotent stem cells isolated from a mesenchymal tissue in a living body or cultured mesenchymal cells. The cell preparation according to the present invention is based on a mechanism whereby the aforesaid disease is ameliorated and treated by administering Muse cells to a subject suffering from the disease and engrafting the cells in lung tissues.

Claims (9)

1. A method of treating persistent pulmonary hypertension of the human newborn (PPHN) and/or hypertension of the human newborn caused by chronic lung disease, the method comprising:

(i) intravenously administering a therapeutically effective amount of human pluripotent stem cells to a human newborn that has PPHN and/or hypertension of the human newborn caused by chronic lung disease,

wherein the human pluripotent stem cells are isolated from mesenchymal tissue, and

wherein the human pluripotent stem cells express SSEA-3 and CD105 but do not express CD117 and CD146, have low or no telomerase activity; have the capability to differentiate into any of three germ layers; exhibit no neoplastic proliferation; and have ability to self-renewal.

2. The method according to claim 1 , wherein the human pluripotent stem cells positive for SSEA-3 have been concentrated by external stress treatment.

3. The method according to claim 1 , wherein the human pluripotent stem cells are CD117-negative, CD146-negative, NG2-negative, CD34-negative, vWF-negative, and CD271-negative.

4. The method according to claim 1 , wherein the human pluripotent stem cells are CD34-negative, CD117-negative, CD146-negative, CD271-negative, NG2-negative, vWF-negative, Sox10-negative, Snail-negative, Slug-negative, Tyrp1-negative, and Dct negative.

5. The method according to claim 1 , wherein the therapeutically effective amount of human pluripotent stem cells is from approximately 1×10 4 cells/individual to approximately 3×10 8 cells/individual.

6. The method according to claim 1 , wherein the therapeutically effective amount of human pluripotent stem cells is approximately 3×10 4 cells/kg to approximately 3×10 7 cells/kg per individual subject.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 8, 2024
From: NATIONAL UNIVERSITY CORPORATION TOKAI NATIONAL HIGHER EDUCATION AND RESEARCH SYSTEM; LIFE SCIENCE INSTITUTE, INC.
To: TOHOKU UNIVERSITY
Reel/Frame 068219/0572 →
CHANGE OF NAME Recorded Aug 8, 2024
From: NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY
To: NATIONAL UNIVERSITY CORPORATION TOKAI NATIONAL HIGHER EDUCATION AND RESEARCH SYSTEM
Reel/Frame 068512/0304 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2019
From: SATO, YOSHIAKI; SUZUKI, TOSHIHIKO; SHIMIZU, SHINOBU; MIZUNO, MASAAKI; HAYAKAWA, MASAHIRO; DEZAWA, MARI
To: NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY; LIFE SCIENCE INSTITUTE, INC.; TOHOKU UNIVERSITY
Reel/Frame 048221/0339 →
Priority Claims (1)
JP 2016-153263 · Aug 3, 2016 · national
Continuity (1)
Related Publication 20190240262A1 · Aug 8, 2019