US2007072291A1PendingUtilityA1
Dedifferentiated, programmable stem cells of monocytic origin, and their production and use
Est. expiryMar 28, 2022(expired)· nominal 20-yr term from priority
A61P 5/00A61P 43/00A61P 9/10A61P 9/02A61P 25/00C12N 2501/20A61L 27/3886C12N 5/0653C12N 2501/23C12N 2501/22C12N 2510/00A61P 17/02C12N 2501/12A61P 1/18A61K 35/15C12N 5/0647C12N 5/069C12N 5/0645C12N 2501/39C12N 2500/44A61P 17/00A61P 1/16C12N 2501/235C12N 2501/117C12N 2500/30C12N 2506/11C12N 2501/33C12N 2501/385A61L 27/3895A61K 35/12C12N 2506/03C12N 5/0676C12N 5/0618A61L 27/3834A61K 2035/124A61L 27/3804C12N 2501/119A61P 11/00C12N 5/0607C12N 5/0619C12N 2501/10C12N 5/0622C12N 2502/14C12N 5/067C12N 2501/11C12N 5/0629A61P 13/12
58
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The invention relates to the production of adult dedifferentiated, programmable stem cells from human monocytes by cultivation of monocytes in a culture medium which contains M-CSF and IL-3. The invention further relates to pharmaceutical preparations, which contain the dedifferentiated, programmable stem cells and the use of these stem cells for the production of target cells and target tissue.
Claims
exact text as granted — not AI-modified1 - 29 . (canceled)
30 . A method of producing a target cell from a dedifferentiated, programmable cell of human monocytic origin comprising:
a) obtaining a desired target cell from a target tissue; b) incubating said desired target cell in a suitable culture medium; and c) providing supernatant from said culture medium after incubation with said desired target cell to dedifferentiated, programmable stem cells of human monocytic origin, wherein said cells express a CD14 antigen and a CD90 antigen to differentiate said cell of human monocytic origin into a target cell.
31 . The method according to claim 30 , wherein said cell of human monocytic origin is differentiated into a adipocyte, a neuron, a glia cell, an endothelial cell, a keratinocyte, a hepatocyte or an islet cell.
32 - 34 . (canceled)
35 . The method according to claim 30 , wherein said target cell also expresses a CD14 antigen.
36 . The method according to claim 30 , wherein said dedifferentiated, programmable cell of human monocytic origin expresses a CD123 antigen.
37 . A method of producing a target cell from a dedifferentiated, programmable cell of human monocytic origin comprising:
a) providing a differentiation medium for differentiation of said dedifferentiated, programmable cell of human monocytic origin, wherein said dedifferentiated, programmable cell expresses a CD14 antigen and a CD90 antigen; and b) differentiating said dedifferentiated, programmable cell of human monocytic origin into a target cell that express a target cell protein.
38 . The method according to claim 37 , wherein said target cell also expresses a CD14 antigen.
39 . The method according to claim 37 , wherein said differentiation medium comprises a factor selected from a group consisting of epidermal growth factor (EGF), hepatocyte growth factor, keratinocyte growth factor, and combinations thereof.
40 . The method according to claim 37 , wherein said target cell protein is albumin.
41 . The method according to claim 37 , wherein said target cell is transfected with a gene.
42 . The method according to claim 37 , wherein said dedifferentiated, programmable cell of human monocytic origin is differentiated into an adipocyte, a neuron, a glia cell, an endothelial cell, a keratinocyte, a hepatocyte or an islet cell.
43 . A method of producing a target cell from a dedifferentiated, programmable cell of human monocytic origin comprising:
a) providing a differentiation medium for differentiation of said dedifferentiated, programmable cell of human monocytic origin, wherein said dedifferentiated, programmable cell expresses a CD14 antigen and a CD90 antigen; and b) differentiating said dedifferentiated, programmable cell of human monocytic origin into said target cell that expresses a target cell protein.
44 . A method of producing a target cell from a dedifferentiated, programmable cell of human monocytic origin comprising administering into a body said dedifferentiated, programmable cell of human monocytic origin, wherein said dedifferentiated, programmable cell of human monocytic origin expresses a CD14 antigen and a CD90 antigen.
45 . The method of claim 44 , wherein said administering is injecting, implanting, or infusing a dedifferentiated, programmable cell of human monocytic origin.
46 . The method of claim 44 , wherein said dedifferentiated, programmable cell of human monocytic origin is in phosphate buffered saline (PBS).
47 . A method of producing a target cell from a dedifferentiated, programmable cell of human monocytic origin comprising:
a) applying to a material said dedifferentiated, programmable cell of human monocytic origin, wherein said dedifferentiated, programmable cell of human monocytic origin expresses a CD14 antigen and a CD90 antigen; and b) administering said material into a body.
48 . The method of claim 47 , wherein said administering is injecting, implanting, or infusing.
49 . The method of claim 47 , wherein said material is selected from the group consisting of a cardiac valve, a vessel prosthesis, a bone prosthesis, a joint prosthesis, a bag, a chamber, and a biodegradable matrix.
50 . A method of treating a patient with a target cell from a dedifferentiated, programmable cell of human monocytic origin comprising:
a) providing a differentiation medium for differentiation of said dedifferentiated, programmable cell of human monocytic origin, wherein said dedifferentiated, programmable cell expresses a CD14 antigen and a CD90 antigen; and b) differentiating said dedifferentiated, programmable cell of human monocytic origin into said target cell that expresses a target cell protein; c) administering said target cell to a patient.
51 . The method of claim 50 , wherein said administering is injecting, implanting, or infusing.
52 . The method of claim 50 , wherein said target cell is administered on a material selected from the group consisting of a cardiac valve, a vessel prosthesis, a bone prosthesis, a joint prosthesis, a bag, a chamber, and a biodegradable matrix.
53 . The method of claim 50 , wherein said patient has a disease selected from the group consisting of cirrhosis of the liver, pancreatic insufficiency, acute or chronic kidney failure, hormonal under-functioning, cardiac infarction, pulmonary embolism, stroke and skin damage.Join the waitlist — get patent alerts
Track US2007072291A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.