IP Library Granted Patent US 8,871,510
Granted Patent B2
US 8,871,510 · App. 13/512,988 · Granted Oct 28, 2014

Methods for generating T lymphocytes from hematopoietic stem cells

Inventors: Gerald John Spangrude (Salt Lake City, UT); Birgitta H. Mitchell (Salt Lake City, UT); Jared Manning (Twin Falls, ID)
Assignee: University of Utah Research Foundation
C12N5/0636C12N2501/23C12N2502/1394C12N5/0646C12N2501/125C12N2502/99C12N2501/26C12N2501/052C12N2501/42C12N2500/38
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Quick Facts
Patent No.
US 8,871,510
App. No.
13/512,988
Granted
Oct 28, 2014
Kind
B2
Abstract

This disclosure describes methods for differentiating T cells and NK cells in vitro from hematopoietic stem cells or precursor cells. The technology is directed to methods for the production of selected populations of lymphocytes, such as T cells and NK cells. The availability of such cell populations allows for the complete reconstitution of a depleted, defective or missing lymphocyte population in a patient.

Claims (16)

1. A method for differentiating mammalian T cells in vitro, the method comprising:

culturing hematopoietic stem cells, hematopoietic progenitor cells, or both hematopoietic stem cells and hematopoietic progenitor cells in a first culture medium for a sufficient time to produce progenitor T cells, wherein the first culture medium lacks ascorbate and comprises cells modified to express a notch ligand configured to direct differentiation of T cells;

transferring the progenitor T cells to a second culture medium comprising ascorbate; and

culturing the progenitor T cells in the second culture medium for a sufficient time to produce differentiated T cells from the progenitor T cells.

2. The method of claim 1 , wherein the first culture medium comprises minimal essential medium (MEM) as the basal culture medium.

3. The method of claim 1 , wherein the first culture medium comprises Iscove's Modified Dulbecco's Medium (IMDM) as the basal culture medium.

4. The method of claim 1 , wherein the second culture medium comprises alpha modification MEM (αMEM) as the basal culture medium.

5. The method of claim 1 , wherein the cells modified to express a notch ligand comprise OP9-DL1 cells.

6. The method of claim 1 , wherein the cells are cultured in the first culture medium for less than about 30 days.

7. The method of claim 1 , wherein the progenitor T cells are cultured in the second culture medium for at least 7 days to produce differentiated T cells from the progenitor T cells.

8. The method of claim 1 , wherein the ascorbate is phosphoascorbate.

9. The method of claim 1 , wherein the ascorbate is present in an effective amount to preferentially differentiate T cells over NK cells.

10. The method of claim 1 , wherein the amount of ascorbate in the second culture medium is from about 10-1000 μg/mL.

11. The method of claim 1 , wherein the first culture medium comprises IL-7, Flt3 ligand, or both IL-7 and Flt3 ligand.

12. The method of claim 1 , wherein the hematopoietic stem cells, the hematopoietic progenitor cells, or both the hematopoietic stem cells and the hematopoietic progenitor cells express CD34.

13. The method of claim 1 , wherein the first culture medium and the second culture medium lack nucleosides.

Assignments (3)
CONFIRMATORY LICENSE Recorded May 18, 2015
From: UNIVERSITY OF UTAH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035709/0673 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2013
From: SPANGRUDE, GERALD JOHN; MITCHELL, BIRGITTA H.; MANNING, JARED
To: UNIVERSITY OF UTAH
Reel/Frame 031228/0982 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2013
From: UNIVERSITY OF UTAH
To: UNIVERSITY OF UTAH RESEARCH FOUNDATION
Reel/Frame 031229/0063 →
Continuity (2)
Provisional Application 61283390 · Dec 3, 2009
Related Publication 20130005035A1 · Jan 3, 2013