IP Library › Granted Patent US 12,486,327
Granted Patent B2
US 12,486,327 · App. 17/442,759 · Granted Dec 2, 2025

CAR for use in the treatment of HvG disease

Inventors: Elmar Jäckel (Hannover, DE); Fatih Noyan (Hannover, DE); Michael Hust (Hannover, DE)
Assignees: Medizinische Hochschule Hannover; Technische Universität Braunschweig
C07K16/2833A61K40/11A61K40/31A61P37/06C07K2317/24C07K2317/53C07K2317/622C07K2317/92C07K2319/03C07K2319/33
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 12,486,327
App. No.
17/442,759
Granted
Dec 2, 2025
Kind
B2
Abstract

The invention provides an optimized and far potent chimeric antigen receptor for its use in the treatment of HvG disease in a patient having received a transplant, for use in suppressing the hosts immune response directed against the transplant. The fusion protein is adapted for use in suppressing the immune rejection of a transplant which contains or expresses HLA-A*02 in a recipient patient who is negative for HLA-A*02, i.e. the patient prior to transplantation does not express HLA-A*02. The fusion protein is a chimeric antigen receptor (CAR), which upon expression in regulatory T-cells (T reg ) causes a specific suppressor activity of the regulatory T-cells in the presence of HLA-A*02.

Claims (25)

1 . A fusion protein comprising a single-chain variable fragment antibody domain (scFv), a hinge, a transmembrane domain, an intracellular hCD28 signalling domain and an intracellular hCD3ζ (hCD3 zeta) signalling domain forming a chimeric antigen receptor having specificity for HLA-A*02 (CAR-A*02) for use in the treatment of HvG disease in a patient, wherein the single-chain variable fragment antibody domain (scFv) has an amino acid sequence which is SEQ ID NO: 9.

2 . The fusion protein according to claim 1 , wherein the intracellular signalling domain comprises a hCD28 signalling domain and an intracellular hCD3ζ (hCD3 zeta) signalling domain.

3 . The fusion protein according to claim 1 , wherein the hinge and the transmembrane domain have the amino acid sequence of SEQ ID NO: 1, the hCD28 signalling domain has the amino acid sequence of SEQ ID NO: 2, and the hCD3ζ (hCD3 zeta) signalling domain has the amino acid sequence of SEQ ID NO: 3.

4 . The fusion protein according to claim 2 , wherein the hinge is a hΔFc IgG domain having the amino acid sequence of SEQ ID NO: 4.

5 . The fusion protein according to claim 1 , wherein the hinge and the transmembrane domain, which is a CD8 hinge and a CD8 transmembrane domain, have the amino acid sequence of SEQ ID NO: 1, the hCD28 signalling domain has the amino acid sequence of SEQ ID NO: 2, and the hCD3ζ domain has the amino acid sequence of SEQ ID NO: 3, or the hCD28 signalling domain including the hCD3ζ signalling domain have the amino acid sequence of SEQ ID NO: 5.

6 . A CD4 + CD25 + CD127 low HLA-A*02 negative human regulatory T (Treg) cell expressing the fusion protein according to claim 1 .

7 . The fusion protein according to claim 1 , wherein the patient is HLA-A*02 negative and in that the patient contains or is intended to contain a solid tissue transplant which is HLA-A*02 positive.

8 . The fusion protein according to claim 1 , wherein a signal peptide of SEQ ID NO: 10 is linked at the N-terminus of SEQ ID NO: 9.

9 . The fusion protein according to claim 1 , comprising or consisting of, from N-terminus to C-terminus, one scFv domain having the amino acid sequence of SEQ ID NO: 9, a hinge and a transmembrane domain having the amino acid sequence of SEQ ID NO: 1, a hCD28 signalling domain having the amino acid sequence of SEQ ID NO: 2, and a hCD3ζ (hCD3 zeta) signalling domain having the amino acid sequence of SEQ ID NO: 3, and a signal peptide of SEQ ID NO: 10 at the N-terminus.

10 . The fusion protein according to claim 1 , comprising or consisting of, from N-terminal to C-terminal, one scFv domain having the amino acid sequence of SEQ ID NO: 9, a hΔFc IgG domain as a hinge having the amino acid sequence of SEQ ID NO: 4, a hCD28 transmembrane domain and a hCD28/hCD3 signalling domain having the amino acid sequence of SEQ ID NO: 5, and a signal peptide of SEQ ID NO: 10 at the N-terminus.

11 . The fusion protein according to claim 1 , expressed from a nucleic acid sequence encoding the fusion protein with optionally an additional N-terminal secretory leader peptide.

12 . The fusion protein according to claim 1 , expressed from a nucleic acid sequence encoding the fusion protein with an additional N-terminal secretory leader peptide and an additional C-terminal P2A-hFOXP3 having the amino acid sequence of SEQ ID NO: 6.

13 . The fusion protein according to claim 11 , wherein the leader peptide has the amino acid sequence of SEQ ID NO: 8.

14 . The fusion protein according to claim 1 , wherein when the fusion protein is expressed in a CD4 + CD25 + CD127 low HLA-A*02 negative human regulatory T (Treg) cell in the presence of HLA-A*02 positive solid tissue, the Treg cell has suppressor activity.

15 . The fusion protein according to claim 1 , wherein when the fusion protein is expressed in a CD4 + CD25 + CD127 low HLA-A*02 negative human regulatory T (Treg) cell, the Treg cell has homing capability to secondary lymphoid organs.

16 . A process for providing a human regulatory T (Treg) cell having suppressor activity in the presence of HLA-A*02 positive solid tissue, comprising the steps of

a. isolating from a blood sample CD4 + CD25 + CD127 low human regulatory T (Treg) cells to produce isolated Treg cells,

b. introducing a nucleic acid sequence encoding and expressing a fusion protein according to claim 1 into the isolated Treg cells to produce Treg cells expressing the fusion protein,

wherein the Treg cells expressing the fusion protein are not expanded in an in vitro culture.

17 . The process according to claim 16 , wherein isolating the human regulatory T cells is isolating HLA-A*02 negative human regulatory T cells.

18 . The process according to claim 16 , wherein the nucleic acid sequence is comprised in a retroviral vector that is packaged in a retroviral particle and is introduced into the isolated Treg cells by transduction.

19 . The process according to claim 16 , wherein following step b., the Treg cells are kept in culture for 24 h, followed by isolating Treg cells expressing the fusion protein.

20 . The process according to claim 19 , wherein the Treg cells are kept in culture in a medium containing low dose IL-2, which medium does not contain an agent stimulating expansion of Treg cells.

21 . A Treg cell containing a nucleic acid construct encoding a fusion protein according to claim 1 .

22 . A method of treating HvG disease in a patient, said method comprising administering to said patient the Treg cell of claim 6 .

Assignments (2)
LICENSE Recorded Nov 17, 2022
From: MEDIZINISCHE HOCHSCHULE HANNOVER; TECHNISCHE UNIVERSITÄT BRAUNSCHWEIG
To: QUELL THERAPEUTICS LIMITED
Reel/Frame 061810/0359 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2021
From: JÄCKEL, ELMAR; NOYAN, FATIH; HUST, MICHAEL
To: MEDIZINISCHE HOCHSCHULE HANNOVER
Reel/Frame 058509/0023 →
Priority Claims (1)
EP 19166421 · Mar 29, 2019 · regional
Continuity (1)
Related Publication 20220289849A1 · Sep 15, 2022
References Cited (38)
US 11160831B2 · Jäckel · 2021 [cited by examiner]
US 20210338726A1 · Martinez-Llordella · 2021 [cited by examiner]
CN 109265550A · 2019 [cited by applicant]
CN 109293773A · 2019 [cited by applicant]
CN 112969784A · 2021 [cited by applicant]
WO 2008095141A2 · 2008 [cited by applicant]
WO WO2013104804A2 · 2013 [cited by applicant]
WO 2015123642A1 · 2015 [cited by applicant]
WO 2017172981A2 · 2017 [cited by applicant]
WO WO2018001874 · 2018 [cited by examiner]
WO WO2018001874A1 · 2018 [cited by applicant]
WO 2018037103A1 · 2018 [cited by applicant]
WO WO2018183293A1 · 2018 [cited by applicant]
WO WO2020044055A1 · 2020 [cited by applicant]
Definition of “characterize”—Merriam Wehbster Online Dictionary, accessed on Mar. 7, 2025, www.merriam-webster.com/ dictionary/characterize. [cited by examiner]
Vajdos et al. (2002) J. Mol. Biol., vol. 320, 415-428. [cited by examiner]
Chen et al. (1992) J. Exp. Med., vol. 176, 855-866. [cited by examiner]
Sela-Culang et al. (2013) Frontiers in Immunology, vol. 4, pp. 1-13. [cited by examiner]
Elinav, et al., “Amelioration of Colitis by Genetically Engineered Murine Regulatory T Cells Redirected by Antigen-Specific Chimeric Receptor”, Gastroenterology, 2009, vol. 136, pp. 1721-1731. [cited by applicant]
Reyes, et al., “Characterization of swine leucocyte antigen alleles in a crossbred pig to be used in xenotransplant studies”, Tissue Antigens, 2014, vol. 84, pp. 484-488. [cited by applicant]
Office Action from EP Application No. 20 713 673.0 dated Jul. 19, 2023. [cited by applicant]
International Search Report from the corresponding International Patent Application No. PCT/EP2017/065472, dated Sep. 1, 2017. [cited by applicant]
Boardman, et al., “Expression of a Chimeric Antigen Receptor Specific for Donor HLA Class I Enhances the Potency of Human Regulatory T Cells in Preventing Human Skin Transplant Rejection”, American Journal of Transplant… [cited by applicant]
Office Action issued in Chinese Application No. 202080034929.X issued on Nov. 29, 2023. [cited by applicant]
Boardman et al., “Expression of a Chimeric Antigen Receptor Specific for Donor HLA Class I Enhances the Potency of Human Regulatory T Cells in Preventing Human Skin Transplant Rejection”, American Journal oF Transplanta… [cited by applicant]
Macdonald et al., “Alloantigen-specific regulatory T cells generated with a chimeric antigen receptor”, The Journal of Clinical Investigation, Apr. 1, 2016, pp. 1413-1424, vol. 126, No. 4. [cited by applicant]
Inaguma et al., “Construction and molecular characterization of a T-cell receptor-like antibody and CAR-T cells specific for minor histocompatibility antigen HA-1H”, Gene Therapy, Apr. 3, 2014, pp. 575-584, vol. 6, No. … [cited by applicant]
Watkins et al., “The isolation and characterisation of human monoclonal HLA-A2 antibodies from an immune V gene phage display library”, Tissue Antigens, Jan. 1, 2000, pp. 219-228. [cited by applicant]
Long et al., “Defects in IL-2R Signaling Contribute to Diminished Maintenance of FOXP3 Expression in CD4+CD25+ Regulatory T-Cells of Type 1 Diabetic Subjects”, Diabetes, Feb. 2010, pp. 407-415, vol. 59. [cited by applicant]
Noyan et al., “Prevention of Allograft Rejection by Use of Regulatory T Cells with an MHC-Specific Chimeric Antigen Receptor”, American Journal of Transplantation, 2017, pp. 917-930, vol. 17. [cited by applicant]
Noyan et al., “Induced Transgene Expression for the Treatment of Solid Tumors by Hematopoietic Stem Cell-Based Gene Therapy”, Cancer Gene Therapy, 2012, pp. 352-357, vol. 19. [cited by applicant]
Galla et al., “Avoiding Cytotoxicity of Transposases by Dose-Controlled mRNA Delivery”, Nucleic Acids Research, 2011, pp. 7147-7160, vol. 39, No. 16. [cited by applicant]
Di Stasi, et al., “Inducible Apoptosis as a Safety Switch for Adoptive Cell Therapy”, The New England Journal of Medicine, Nov. 3, 2011, pp. 1673-1683, vol. 365. No. 18. [cited by applicant]
Hombach et al., “Adoptive Immunotherapy with Genetically Eingeered T cells: modification of the IgG1 Fc 'spacer Domain in the Extracellular Moiety of Chimeric Antigen Receptors Avoids ‘off-target’ Activation and Uninten… [cited by applicant]
PCT Notification of Transmittal of the International Search Report and the Written Opinion of the International Searching Authority, or the Declaration dated May 27, 2020 for PCT Application No. PCT/EP2020/059000. [cited by applicant]
Chinese Office Action from the corresponding Chinese Patent Application No. 202080034929, dated Jun. 28, 2024. [cited by applicant]
Fransson, et al., “CAR/FoxP3-engineered T regulatory cells target the CNS and suppress EAE upon intranasal delivery”, Journal of Neuroinflammation, 2012, 9:112, pp. 1-12. [cited by applicant]
Noyan, et al,. “Isolation of human antigen-specific regulatory T cells with high suppressive function”, Eur. J. Immunol., 2014, 44, pp. 2592-2602. [cited by applicant]