US2020131475A1PendingUtilityA1
Method of generating natural killer cells and dendritic cells from human embryonic stem cell-derived hemangioblasts
Assignee: ASTELLAS INST FOR REGENERATIVE MEDICINEPriority: Dec 4, 2009Filed: Oct 31, 2019Published: Apr 30, 2020
Est. expiryDec 4, 2029(~3.3 yrs left)· nominal 20-yr term from priority
C12N 2501/22A61K 2035/124C12N 2506/02C12N 2501/2303C12N 2501/2304A61P 35/00C12N 2501/26C12N 2501/23C12N 2501/125A61P 37/04A61K 35/15C12N 5/0639C12N 5/0646C12N 2501/115C12N 2501/145C12N 2501/165C12N 2501/155C12N 2501/2315C12N 2501/2307C12N 2501/2302A61K 40/42A61K 40/15A61K 2239/48A61K 35/17
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Claims
Abstract
This invention provides methods of generating natural killer (NK) cells and dendritic cells (DCs). The methods utilize human hemangioblasts as intermediate cells to generate the NK cells and DCs. In various embodiments, the methods do not require the use of stromal feeder layers.
Claims
exact text as granted — not AI-modified1 - 38 . (canceled)
39 . A method of producing natural killer (NK) cells, the method comprising culturing a hemangioblast under feeder free conditions in a first culture media comprising at least two growth factors selected from the group consisting of SCF, Flt3-ligand (FL), and IL3, thereby producing an NK cell.
40 . The method of claim 39 , wherein the first culture media is a liquid media.
41 . The method of claim 39 , wherein the first culture media is a semi-solid media.
42 . The method of claim 41 , wherein the semi-solid media comprises methylcellulose.
43 . The method of claim 42 , wherein the semi-solid media lacks erythropoietin.
44 . The method of claim 39 , wherein the first culture media further comprises at least one additional growth factor selected from the group consisting of IL2, IL6, IL7, and IL15.
45 . The method of claim 39 , further comprising culturing the hemangioblast under feeder free conditions in a second culture media comprising at least one growth factor selected from the group consisting of IL7, IL15, SCF, and FL.
46 . The method of claim 45 , wherein the second culture media is a liquid media.
47 . The method of claim 39 , wherein the hemangioblast is obtained from a pluripotent stem cell.
48 . The method of claim 47 , wherein the pluripotent stem cell is a human embryonic stem cell or a human induced pluripotent stem cell.
49 . The method of claim 47 , wherein the hemangioblast is obtained from a pluripotent stem cell under feeder-free conditions.
50 . The method of claim 47 , wherein the hemangioblast is obtained from a pluripotent stem cell without culturing with erythropoietin.
51 . The method of claim 39 , wherein the NK cells are CD56+.
52 . The method of claim 39 , wherein the NK cells are CD56−.
53 . The method of claim 39 , wherein the first culture media is serum-free.
54 . A method of producing a human pluripotent stem cell-derived natural killer (NK) cell, the method comprising
(a) differentiating a human pluripotent stem cell to a precursor cell capable of differentiating to give rise to at least hematopoietic cell types, endothelial cell types, or mesodermal derivatives under feeder free conditions in at least one culture media comprising at least one growth factor selected from the group consisting of bone morphogenetic protein 4 (BMP4), vascular endothelial growth factor (VEGF), and bFGF; and (b) differentiating the precursor cell to an NK cell under feeder free conditions in at least one culture media comprising at least two growth factors selected from the group consisting of SCF, Flt3-ligand (FL), and IL3.
55 . The method of claim 54 , wherein the human pluripotent stem cell is a human embryonic stem cell or a human induced pluripotent stem cell.
56 . The method of claim 54 , wherein the NK cell is CD56+.
57 . The method of claim 54 , wherein the at least one culture media of step (a) is serum-free.
58 . The method of claim 54 , wherein the at least one culture media of step (b) further comprises at least one additional growth factor selected from the group consisting of IL2, IL6, IL7, and IL15.
59 . The method of claim 54 , wherein the at least one culture media of steps (a) and (b) lack erythropoietin.
60 . The method of claim 54 , further comprising differentiating the precursor cell to an NK cell under feeder free conditions in step (b) in a second culture media comprising IL7, IL15, SCF, and FL.
61 . The method of claim 54 , wherein the precursor cell of step (a) is harvested before step (b).
62 . A method of producing a natural killer (NK) cell, the method comprising
(a) differentiating an embryoid body to a precursor cell capable of differentiating to give rise to at least hematopoietic cell types, endothelial cell types, or mesodermal derivatives under feeder-free conditions in at least one culture media comprising at least two growth factors selected from the group consisting of TPO, vascular endothelial growth factor (VEGF), and Flt3-ligand (FL); and (b) differentiating the precursor cell to an NK cell under feeder-free conditions in at least one culture media comprising at least three growth factors selected from the group consisting of SCF, FL, IL3, IL7, IL2, and IL6.
63 . The method of claim 62 , wherein the embryoid body is obtained from a pluripotent stem cell.
64 . The method of claim 63 , wherein the pluripotent stem cell is a human embryonic stem cell or a human induced pluripotent stem cell.
65 . The method of claim 62 , wherein the NK cell is CD56+.
66 . The method of claim 62 , wherein the at least one culture media of step (a), (b), or both are serum-free.
67 . The method of claim 62 , wherein the at least one culture media of steps (a) and (b) lack erythropoietin.
68 . The method of claim 62 , wherein the precursor cell of step (a) is harvested before step (b).
69 . A method of producing a natural killer (NK) cell, the method comprising
(a) culturing an embryoid body in a culture media comprising bone morphogenetic protein 4 (BMP4), vascular endothelial growth factor (VEGF), and bFGF; and (b) culturing the product of step (a) in a culture media comprising at least two growth factors selected from the group consisting of TPO, VEGF, and Flt3-ligand (FL); (c) culturing the product of (b) in a culture media comprising at least three growth factors selected from the group consisting of SCF, FL, IL3, IL7, IL2, and IL6, thereby generating an NK cell; wherein the culturing is conducted under feeder-free conditions throughout steps (a)-(c) of the method.
70 . The method of claim 69 , wherein the embryoid body is obtained from a pluripotent stem cell.
71 . The method of claim 69 , wherein the pluripotent stem cell is a human embryonic stem cell or a human induced pluripotent stem cell.
72 . The method of claim 69 , wherein the NK cell is CD56+.
73 . The method of claim 69 , wherein the culture media of step (a), (b), and/or (c) are serum-free.
74 . The method of claim 69 , wherein the culture media of steps (a), (b), and (c) lack erythropoietin.
75 . A method of producing a human pluripotent stem cell-derived natural killer (NK) cell, the method comprising
differentiating a human pluripotent stem cell to an NK cell under feeder-free conditions in a series of culture media, wherein (i) a first culture media is a serum-free culture media comprising at least two growth factors selected from the group consisting of bone morphogenetic protein 4 (BMP4), vascular endothelial growth factor (VEGF), and bFGF; (ii) a second culture media is a serum-free culture media comprising at least two growth factors selected from the group consisting of TPO, VEGF, Flt3-ligand (FL), bFGF, IL2, IL7, and IL15; and (iii) a third culture media comprises at least three growth factors selected from the group consisting of SCF, FL, IL3, IL7, IL2, and IL6, thereby generating an NK cell.
76 . The method of claim 75 , wherein the human pluripotent stem cell is a human embryonic stem cell or a human induced pluripotent stem cell.
77 . The method of claim 75 , wherein the NK cell is CD56+.
78 . The method of claim 75 , wherein the first culture media, the second culture media, and the third culture media lack erythropoietin.Join the waitlist — get patent alerts
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