IP Library Granted Patent US 9,808,485
Granted Patent B2
US 9,808,485 · App. 13/345,036 · Granted Nov 7, 2017

Immunomodulatory properties of multipotent adult progenitor cells and uses thereof

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Quick Facts
Patent No.
US 9,808,485
App. No.
13/345,036
Granted
Nov 7, 2017
Kind
B2
Abstract

Isolated cells are described that are not embryonic stem cells, not embryonic germ cells, and not germ cells. The cells can differentiate into at least one cell type of each of at least two of the endodermal, ectodermal, and mesodermal lineages. The cells do not provoke a harmful immune response. The cells can modulate immune responses. As an example, the cells can suppress an immune response in a host engendered by allogeneic cells, tissues, and organs. Methods are described for using the cells, by themselves or adjunctively, to treat subjects. For instance, the cells can be used adjunctively for immunosuppression in transplant therapy. Methods for obtaining the cells and compositions for using them also are described.

Claims (28)

1. A method of treatment of diabetes in a subject, comprising: administering to a subject in need of treatment for diabetes—by an effective route and in an effective amount to treat diabetes, cells that: are not embryonic stem cells, embryonic germ cells, or germ cells; can differentiate into at least one cell type of each of at least two of the endodermal, ectodermal, and mesodermal embryonic lineages; express telomerase; are allogeneic or xenogeneic to the subject; do not provoke a deleterious immune response in the subject; and are effective to treat diabetes in the subject,—wherein the cells are administered adjunctively to one or more other treatments, without also administering an immunosuppressive treatment adjunctively to treatment with the cells wherein the cells have not been genetically engineered to improve their immunomodulatory properties.

2. A method according to claim 1 , wherein said cells can differentiate into at least one cell type of each of the endodermal, ectodermal, and mesodermal embryonic lineages.

3. A method according to claim 1 , wherein said cells are positive for oct-3/4.

4. A method according to claim 1 , wherein said cells have undergone at least 10 to 40 cell doublings in culture prior to their administration to the subject.

5. A method according to claim 1 , wherein said cells are allogeneic to the subject.

6. A method according to claim 1 , wherein said cells are administered to the subject adjunctively to another treatment that is administered before, at the same time as, or after said cells are administered.

7. A method according to claim 1 , wherein said cells are mammalian cells.

8. A method according to claim 7 , wherein said cells are human cells.

9. A method according to claim 7 , wherein said cells are derived from cells isolated from placental tissue, umbilical cord tissue, umbilical cord blood, bone marrow, blood, spleen tissue, thymus tissue, spinal cord tissue, or liver tissue.

10. A method according to claim 1 , wherein the subject is a mammal.

11. A method according to claim 10 , wherein the subject is human.

12. A method according to claim 11 , wherein said cells are administered to the subject in one or more doses comprising 10 4 to 10 8 of said cells per kilogram of the subject's mass.

13. A method according to claim 1 , wherein the diabetes is Type I diabetes mellitus.

14. A method according to claim 13 , wherein said cells can differentiate into at least one cell type of each of the endodermal, ectodermal, and mesodermal embryonic lineages.

15. A method according to claim 13 , wherein said cells are positive for oct-3/4.

16. A method according to claim 13 , wherein said cells have undergone at least 10 to 40 cell doublings in culture prior to their administration to the subject.

17. A method according to claim 13 , wherein said cells are allogeneic to the subject.

18. A method according to claim 13 , wherein said cells are mammalian cells.

19. A method according to claim 13 , wherein said cells are human cells.

20. A method according to claim 13 , wherein said cells are derived from cells isolated from placental tissue, umbilical cord tissue, umbilical cord blood, bone marrow, blood, spleen tissue, thymus tissue, spinal cord tissue, or liver tissue.

21. A method according to claim 13 , wherein the subject is a mammal.

22. A method according to claim 13 , wherein the subject is human.

23. A method according to claim 13 , wherein said cells are administered to the subject in one or more doses comprising 10 4 to 10 8 of said cells per kilogram of the subject's mass.

24. A method according to claim 13 , wherein the diabetes is Type I diabetes mellitus.

25. A method according to claim 1 , wherein the cells are derived from bone marrow.

26. A method according to claim 25 , wherein the cells are derived from human bone marrow.

27. A method according to claim 13 , wherein the cells are derived from bone marrow.

28. A method according to claim 27 , wherein the cells are derived from human bone marrow.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2024
From: ABT HOLDING COMPANY; ATHERSYS, INC.; ADVANCED BIOTHERAPEUTICS, INC.; REGENESYS BVBA; REGENESYS, LLC
To: HEALIOS K.K.
Reel/Frame 067606/0139 →
RELEASE OF SECURITY INTEREST Recorded May 29, 2024
From: HEALIOS K.K.
To: ABT HOLDING COMPANY; ATHERSYS, INC.; ADVANCED BIOTHERAPEUTICS, INC.; REGENESYS BVBA; REGENESYS, LLC
Reel/Frame 067566/0638 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 1, 2024
From: ABT HOLDING COMPANY; ATHERSYS, INC.; ADVANCED BIOTHERAPEUTICS, INC.; REGENESYS BVBA; REGENESYS, LLC
To: HEALIOS K.K.
Reel/Frame 066435/0775 →
CHANGE OF NAME Recorded Jun 24, 2019
From: ATHERSYS, INC.
To: ABT HOLDING COMPANY
Reel/Frame 049564/0986 →