IP Library Granted Patent US 11,560,426
Granted Patent B2
US 11,560,426 · App. 16/618,881 · Granted Jan 24, 2023

Targeting modules for universal chimeric antigen receptor expressing immune cells and use in the treatment of cancer infections and autoimmune disorders

Inventor: Armin Ehninger (Dresden, DE)
Assignee: AvenCell Europe GmbH
C07K16/28A61K38/105A61K38/1883A61K38/2207A61K38/2278A61K38/26A61K38/31A61K47/62C07K14/55C07K14/7051C07K14/70521C07K14/70578A61K38/00C07K2317/24C07K2317/53C07K2317/622C07K2319/02C07K2319/03C07K2319/30C07K2319/33
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,560,426
App. No.
16/618,881
Granted
Jan 24, 2023
Kind
B2
Abstract

The present invention relates to a targeting module comprising a chemically synthesized peptide binding moiety specific for a human cell surface protein or protein complex, a kit comprising the targeting module and a vector or a cell comprising a nucleic acid encoding a universal chimeric antigen receptor and the use for the treatment of cancer, infections and autoimmune disorders.

Claims (37)

1. A targeting module comprising:

a glutamate-urea-lysine motif,

a chelator, and

a tag, wherein the tag comprises a human nuclear La protein epitope selected from SEQ ID NOs: 25 and 27.

2. The targeting module according to claim 1 , selected from

which contains SEQ ID NO: 28, and

which contains SEQ ID NO: 27,

wherein Z is a chelator

n is an integer

is 2 or more.

3. A pharmaceutical composition comprising a targeting module according to claim 1 .

4. A method for the treatment of a prostate specific membrane antigen expressing cancer comprising administering to a patient the targeting module according to claim 1 and a vector or a cell comprising a nucleic acid encoding a universal chimeric antigen receptor that comprises:

a tag-binding domain comprising

a variable region heavy chain comprising SEQ ID NO: 21 and a variable region light chain comprising SEQ ID NO: 22, or

a variable region heavy chain comprising SEQ ID NO: 23 and a variable region light chain comprising SEQ ID NO: 24;

an extracellular hinge and a transmembrane domain; and

a signal transduction domain.

5. The method of claim 4 , wherein the targeting module has a structure selected from

which contains SEQ ID NO: 25, and

which contains SEQ ID NO: 27

wherein Z is a chelator

n is an integer

is 2 or more.

6. The method of claim 4 , wherein the extracellular hinge and transmembrane domain is selected from hinge and transmembrane domains of human CD28 molecule, CD8a chain NK cell receptors, parts of the constant region of an antibody, and combinations thereof.

7. The method of claim 4 , wherein the signal transduction domain is selected from the group consisting of cytoplasmic regions of CD28, CD137 (4-1BB), CD134 (OX40), DAP10 and CD27, programmed cell death-1 (PD-1), cytotoxic T-lymphocyte antigen 4 (CTLA-4), cytoplasmic regions of CD3 chains, DAP12, and activating Fc receptors.

8. The method of claim 4 , wherein the nucleic acid comprises a nucleotide sequence according to SEQ ID NO: 1, 9, 13 or 16 encoding for a universal chimeric antigen receptor with an amino acid sequence according to SEQ ID NO: 17, 18, 19, or 20.

9. A kit comprising

a) a targeting module according to claim 1 and

b) a vector or a cell comprising a nucleic acid encoding a universal chimeric antigen receptor that comprises:

a tag-binding domain comprising

a variable region heavy chain comprising SEQ ID NO: 21 and a variable region light chain comprising SEQ ID NO: 22, or

a variable region heavy chain comprising SEQ ID NO: 23 and a variable region light chain comprising SEQ ID NO: 24;

an extracellular hinge and a transmembrane domain; and

a signal transduction domain.

10. The kit according to claim 9 , wherein the extracellular hinge and transmembrane domain is selected from hinge and transmembrane domains of human CD28 molecule, CD8a chain NK cell receptors parts of the constant region of an antibody, and combinations thereof.

11. The kit according to claim 9 , wherein the signal transduction domain is selected from the group consisting of cytoplasmic regions of CD28, CD137 (4-1BB), CD134 (OX40), DAP10 and CD27, programmed cell death-1 (PD-1), cytotoxic T-lymphocyte antigen 4 (CTLA-4), cytoplasmic regions of CD3 chains, DAP12, and activating Fc receptors.

12. The kit according to claim 9 , wherein the nucleic acid comprises a nucleotide sequence according to SEQ ID NO: 1, 9, 13 or 16 encoding for a universal chimeric antigen receptor with an amino acid sequence according to SEQ ID NO: 17, 18, 19, or 20.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Oct 18, 2024
From: BXLS V – DIAMANT L.P.
To: AVENCELL THERAPEUTICS, INC.
Reel/Frame 068941/0187 →
SECURITY INTEREST Recorded Jan 4, 2024
From: AVENCELL THERAPEUTICS, INC.
To: BXLS V - DIAMANT L.P., AS COLLATERAL AGENT
Reel/Frame 066026/0610 →
CHANGE OF NAME Recorded Mar 17, 2022
From: GEMOAB GMBH
To: AVENCELL EUROPE GMBH
Reel/Frame 059390/0606 →
CHANGE OF NAME Recorded Nov 23, 2021
From: GEMOAB MONOCLONALS GMBH
To: GEMOAB GMBH
Reel/Frame 058566/0170 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 3, 2019
From: EHNINGER, ARMIN
To: GEMOAB MONOCLONALS GMBH
Reel/Frame 051163/0010 →
Priority Claims (1)
EP 17175124 · Jun 9, 2017 · regional
Continuity (1)
Related Publication 20200131262A1 · Apr 30, 2020