IP Library Granted Patent US 10,696,950
Granted Patent B2
US 10,696,950 · App. 16/370,606 · Granted Jun 30, 2020

Treating diabetes with genetically modified beta cells

Inventors: Gerald F. Swiss (Rancho Santa Fe, CA); David Kiewlich (Alameda, CA)
Assignee: Wallkill BioPharma, Inc.
C12N5/0676A61K35/17A61K35/39A61P3/10C07K14/522C12N5/0635C12N5/0638C12N5/0646C12N5/0686C12N2501/998C12N2502/11C12N2510/00
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Quick Facts
Patent No.
US 10,696,950
App. No.
16/370,606
Granted
Jun 30, 2020
Kind
B2
Abstract

Described herein are human transgenic beta cells expressing fugetactic levels of CXCL12 to a subject in need thereof. Also described herein are beta cells comprising a transgene comprising a nucleic acid sequence encoding CXCL12.

Claims (13)

1. A population of isolated genetically engineered human beta cells comprising a nucleic acid encoding for exogenous or heterologous expression of a human CXCL12 protein beta isoform such that said population of said cells is characterized as being resistant to cell death when in the presence of human immune cells in vitro as compared to a population of unengineered human beta cells obtained from a human stem cell that has been differentiated ex vivo into human beta cells,

wherein said characterization is based on the relative amounts of lipase dehydrogenase (LDH) measured after assaying said population of engineered cells for 24 hours in the presence of human peripheral blood mononuclear cells (PBMCs) at a ratio of 1:30 genetically engineered beta cells to PBMCs,

wherein the amount of LDH is decreased by at least 95% for said population of engineered human beta cells compared to that of a population of unengineered human beta cells,

wherein the nucleic acid is operably linked to an exogenous promoter,

wherein the population of genetically engineered human beta cells is insulin producing and has been exposed to a senescence inducing agent, and

wherein the population of genetically engineered human beta cells is obtained from a human stem cell that has been differentiated ex vivo into a human beta cell and said population of genetically engineered human beta cells is allogeneic or autologous.

2. The population of isolated genetically engineered human beta cells of claim 1 , wherein the human CXCL12 protein isoform comprises SEQ ID NO: 2.

3. The population of isolated genetically engineered human beta cells of claim 2 ,

wherein said population of isolated genetically engineered human beta cells is an induced pluripotent stem (iPS) cell that is an allogeneic iPS differentiated into a human beta cell.

4. The population of claim 1 , wherein said characterization is based on the relative amounts of LDH measured after assaying said population of engineered cells for 48 hours in the presence of PMBCs.

5. The population of claim 1 , wherein the nucleic acid is heterologous.

6. The population of claim 1 , wherein said population of genetically engineered human beta cells is autologous.

7. The population of claim 1 , wherein said population of genetically engineered human beta cells is allogeneic.

Assignments (2)
CHANGE OF NAME Recorded Jul 30, 2020
From: WALLKILL BIOPHARMA INC.
To: SDF BIOPHARMA INC.
Reel/Frame 053365/0714 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2020
From: SWISS, GERALD F.; KIEWLICH, DAVID
To: WALLKILL BIOPHARMA, INC.
Reel/Frame 051549/0551 →
Continuity (11)
Continuation 16146980 · Sep 28, 2018
Provisional Application 62734910 · Sep 21, 2018
Provisional Application 62719975 · Aug 20, 2018
Provisional Application 62717587 · Aug 10, 2018
Provisional Application 62696603 · Jul 11, 2018
Provisional Application 62694634 · Jul 6, 2018
Provisional Application 62662651 · Apr 25, 2018
Provisional Application 62637913 · Mar 2, 2018
Provisional Application 62568117 · Oct 4, 2017
Provisional Application 62567604 · Oct 3, 2017
Related Publication 20190218518A1 · Jul 18, 2019
Cited By (1)
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