IP Library › Granted Patent US 11,471,517
Granted Patent B2
US 11,471,517 · App. 16/598,914 · Granted Oct 18, 2022

Compositions and methods for preventing and treating graft versus host disease

Inventors: Jonathan Serody (Chapel Hill, NC); James Coghill (Chapel Hill, NC); Danny Bruce (Chapel Hill, NC); Bruce Blazar (Golden Valley, MN); Heather Stefanski (Minneapolis, MN); Benjamin Vincent (Chapel Hill, NC)
Assignees: The University of North Carolina at Chapel Hill; Regents of the University of Minnesota
A61K39/001A61K35/17A61K35/28A61P11/00C12N5/0634C12N5/0651A61K2035/122A61K2035/124A61K2039/5154A61K2039/577C12N2501/2307C12N2501/2333
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Quick Facts
Patent No.
US 11,471,517
App. No.
16/598,914
Granted
Oct 18, 2022
Kind
B2
Abstract

ILC2 cells play a role in the pathogenesis of graft versus host disease (GvHD) and idiopathic pneumonia syndrome (IPS), both conditions associated with allogeneic stem cell transplantation. Infusion of IL-33 activated ILC2 cells into patients with ongoing GvHD or IPS, or prior to onset of GvHD or IPS in susceptible patients, substantially ameliorates the disease and improves survival.

Claims (13)

1. A method for treating acute graft versus host disease (GvHD) in a subject, comprising:

providing a subject in need of treatment for acute GvHD; and

administering to the subject a therapeutically effective amount of a cell preparation of IL-33 activated ILC2 cells.

2. The method of claim 1 , wherein the ILC2 cells have the following properties:

positive for expression of lymphoid marker CD90;

positive for expression of lymphoid marker ICOS; and

negative for expression of lymphoid marker lin.

3. The method of claim 2 , wherein the ILC2 cells are positive for expression of CD127, ST2, Sca-1, CD25, CD90, and ICOS, and negative for expression of lin.

4. The method of claim 1 , wherein the subject is a human subject receiving an allogeneic stem cell transplant (allo-SCT) or allogeneic bone marrow transplant (allo-BMT).

5. The method of claim 1 , wherein the cell preparation of IL-33 activated ILC2 cells is administered to the subject within 1 to 30 days after receiving the allo-SCT or allo-BMT.

6. The method of claim 1 , wherein the risk and/or severity of acute GVHD associated with allo-SCT or allo-BMT is reduced.

7. The method of claim 1 , wherein the cell preparation of IL-33 activated ILC2 cells is administered as a co-infusion with the allo-SCT or allo-BMT.

8. The method of claim 1 , wherein production of Th2 cytokines in the subject is increased, and/or production of Th1 and/or Th17 cytokines in the subject is decreased.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 13, 2020
From: BLAZAR, BRUCE; STEFANSKI, HEATHER
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 052111/0210 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 13, 2020
From: SERODY, JONATHAN; COGHILL, JAMES; BRUCE, DANNY; VINCENT, BENJAMIN
To: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
Reel/Frame 052112/0311 →
Continuity (3)
Division 15532740
Provisional Application 62087340 · Dec 4, 2014
Related Publication 20200155656A1 · May 21, 2020