IP Library Granted Patent US 11,407,802
Granted Patent B2
US 11,407,802 · App. 16/389,423 · Granted Aug 9, 2022

Compositions and methods of chimeric autoantibody receptor T cells

Inventors: Aimee S. Payne (Merion Station, PA); Christoph T. Ellebrecht (Philadelphia, PA); Vijay Bhoj (Philadelphia, PA); Michael C. Milone (Cherry Hill, NJ)
Assignee: The Trustees of the University of Pennsylvania
C07K14/705A61K39/0008A61K48/00C07K16/28A61K2039/5158A61K2039/57C07K2319/02C07K2319/03
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Quick Facts
Patent No.
US 11,407,802
App. No.
16/389,423
Granted
Aug 9, 2022
Kind
B2
Abstract

The invention includes compositions comprising at least one chimeric autoantibody receptor (CAAR) specific for an autoantibody, vectors comprising the same, compositions comprising CAAR vectors packaged in viral particles, and recombinant T cells comprising the CAAR. The invention also includes methods of making a genetically modified T cell expressing a CAAR (CAART) wherein the expressed CAAR comprises a desmoglein extracellular domain.

Claims (14)

1. A genetically modified cell comprising a chimeric receptor comprising an extracellular domain comprising Dsg1, Dsg3, or a fragment thereof that binds an autoantibody expressed on a B-cell, and a transmembrane domain, wherein the cell expresses the chimeric receptor and binds the autoantibody expressed on the B-cell or induces killing of the B-cell expressing the autoantibody.

2. The cell of claim 1 , wherein the cell is selected from the group consisting of a helper T cell, a cytotoxic T cell, a memory I cell, a regulatory T cell, a gamma delta T cell, a natural killer cell, a cytokine induced killer cell, and a cell line thereof.

3. The cell of claim 1 , wherein the extracellular domain comprises Dsg3 or a fragment thereof.

4. The cell of claim 3 , wherein the extracellular domain comprises an amino acid sequence selected from the group consisting of SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, and SEQ ID NO:12, or an amino acid sequence encoded by the nucleotide sequence of SEQ ID NO:36.

5. The cell of claim 1 , wherein the chimeric receptor further comprises a CD8 alpha chain signal peptide.

6. The cell of claim 5 , wherein the CD8 alpha chain signal peptide comprises the amino acid sequence of SEQ ID NO:1.

7. The cell of claim 1 , wherein the extracellular domain comprises Dsg3 or a fragment thereof and the chimeric receptor further comprises a propeptide of Dsg3.

8. The cell of claim 1 , wherein the transmembrane domain comprises a KIR transmembrane domain.

9. The cell of claim 1 , wherein the transmembrane domain comprises a CD8 alpha chain hinge and transmembrane domain.

10. The cell of claim 9 , wherein the CD8 alpha chain hinge and transmembrane domain comprises the amino acid sequence of SEQ ID NO:13.

11. The cell of claim 1 , wherein the chimeric receptor further comprises a peptide linker.

12. The cell of claim 11 , wherein the peptide linker comprises the amino acid sequence of SEQ ID NO:14.

13. The cell of claim 1 , wherein the chimeric receptor further comprises a KIR cytoplasmic domain.

14. The cell of claim 1 , wherein the cell has limited toxicity toward a healthy cell.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 10, 2023
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 064548/0678 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2023
From: PAYNE, AIMEE S.; ELLEBRECHT, CHRISTOPH T.; BHOJ, VIJAY; MILONE, MICHAEL C.
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 062409/0256 →
Continuity (3)
Continuation 15307644
Provisional Application 61987989 · May 2, 2014
Related Publication 20190309041A1 · Oct 10, 2019