IP Library › Granted Patent US 11,662,343
Granted Patent B2
US 11,662,343 · App. 16/603,454 · Granted May 30, 2023

Cellular populations and uses thereof

Inventors: Geoffrey R. Hill (Herston, AU); Ping Zhang (Herston, AU)
Assignee: THE COUNCIL OF THE QUEENSLAND INSTITUTE OF MEDICAL RESEARCH
G01N33/505C07K14/535C07K14/5412C07K14/5428C07K14/5446C07K14/70514C12N5/0637
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Quick Facts
Patent No.
US 11,662,343
App. No.
16/603,454
Granted
May 30, 2023
Kind
B2
Abstract

Disclosed are methods of identifying immunosuppressive T R 1 regulatory T cells, including in methods of diagnosing the presence of immune tolerance, methods of producing immunosuppressive regulatory T cells, and methods of eliciting immune tolerance in a subject. These methods include screening T cells to detect Eomes + IL-10 + T cells or expressing recombinant Eomes in T cell populations to generate immunosuppressive regulatory T cells.

Claims (13)

1. A method of producing a population of immunosuppressive regulatory T cells, the method comprising: isolating a heterogenous population of cells comprising regulatory T cells; enriching for IL-10 + CD4 + T cells that are optionally positive or high for at least one of CD122, α4β7, LAG-3, Ly6C and TIGIT, and/or optionally negative or low for one or more of CD25, CD69 and FoxP3; and introducing into the IL-10 + CD4 + T cells a construct comprising an Eomes coding sequence in operable connection with a regulatory sequence that is operable in the IL-10 + CD4 + T cells, to thereby produce a population of immunosuppressive regulatory T cells comprising Eomes + IL-10 + CD4 + T cells.

2. The method claim 1 , further comprising expanding the Eomes + IL-10 + CD4 + T cells.

3. The method of claim 2 , wherein the Eomes + IL-10 + CD4 + T cells are expanded by a process comprising contacting the Eomes + IL-10 + CD4 + T cells with an agent selected from the group consisting of an antigen, an alloantigen, an anti-CD3 antibody and an anti-CD28 antibody.

4. The method of claim 2 , wherein the Eomes + IL-10 + CD4 + T cells comprise Eomes + IL-10 + CD4 + T cells that are antigen-specific.

5. The method of claim 1 , wherein the Eomes + IL-10 + CD4 + T cells comprise Eomes hi T cells.

6. The method of claim 1 , wherein the Eomes + IL-10 + CD4 + T cells comprise Tbet lo T cells.

7. The method of claim 1 , wherein the Eomes + IL-10 + CD4 + T cells comprise IFNγ + T cells.

8. The method of claim 1 , wherein the Eomes + IL-10 + CD4 + T cells are high for one or both of IL-10 and IFNγ.

9. The method of claim 1 , wherein the Eomes + IL-10 + CD4 + T cells are negative or low for T H 2 cytokines.

10. The method of claim 1 , wherein the Eomes + IL-10 + CD4 + T cells are capable of suppressing at least one immune function selected from the group consisting of IL-2 production, cell proliferation, cytokine production, cell migration, and effector functions, killing, and T-cell proliferation.

11. A method of eliciting immune tolerance in a subject, the method comprising preparing a population of immunosuppressive regulatory T cells produced according to the method of claim 1 and administering the immunosuppressive regulatory T cells to the subject to thereby suppress an immune response in the subject.

12. The method of claim 11 , wherein the population of immunosuppressive regulatory T cells is autologous or allogeneic to the subject.

13. The method of claim 11 , wherein the subject has an immune or autoimmune disorder.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2020
From: HILL, GEOFFREY R.; ZHANG, PING
To: THE COUNCIL OF THE QUEENSLAND INSTITUTE OF MEDICAL RESEARCH
Reel/Frame 053083/0450 →
Priority Claims (1)
AU 2017901292 · Apr 7, 2017 · national
Continuity (1)
Related Publication 20200150108A1 · May 14, 2020