IP Library › Granted Patent US 11,779,638
Granted Patent B2
US 11,779,638 · App. 17/853,334 · Granted Oct 10, 2023

Method of eliciting a CD8+ cytotoxic response in hepatocellular carcinoma patients with a population of activated T cells

Inventors: Toni Weinschenk (Tuebingen, DE); Andrea Mahr (Tuebingen, DE); Jens Fritsche (Tuebingen, DE); Phillip Mueller (Tuebingen, DE); Anita Wiebe (Tuebingen, DE); Sarah Kutscher (Tuebingen, DE)
Assignee: IMMATICS BIOTECHNOLOGIES GMBH
A61K39/00111A61K35/17A61K38/04A61K39/0011A61K51/1057C07K7/00C07K7/06C07K7/08C07K14/435C07K14/7051C07K14/70539C07K16/18C12N5/0636C12N15/115G01N33/6803A61K2035/124A61K2039/5154A61K2039/5158C07K2317/70C07K2319/40C12N2310/16C12N2501/998
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Quick Facts
Patent No.
US 11,779,638
App. No.
17/853,334
Granted
Oct 10, 2023
Kind
B2
Abstract

A method of eliciting an immune response in a patient who has a cancer includes administering to said patient a composition containing a population of activated T cells that selectively recognize the cancer cells in the patient that aberrantly express a peptide consisting of the amino acid sequence of IYVTSIEQI (SEQ ID NO: 214), in which the peptide is in a complex with an MHC molecule.

Claims (28)

1. A method of eliciting a CD8+cytotoxic T cell response in an HLA-A*24+patient who has cancer that presents at the cell surface a peptide consisting of the amino acid sequence of IYVTSIEQI (SEQ ID NO: 214), comprising

administering to said identified patient a composition comprising a population of activated antigen-specific CD8+cytotoxic T cells to kill the cancer cells in the identified patient,

wherein the population of activated antigen-specific CD8+cytotoxic T cells recognize the cancer cells by interacting through their T cell receptor (TCR) with a peptide consisting of the amino acid sequence of IYVTSIEQI (SEQ ID NO: 214) in a complex with HLA-A*24 presented at the surface of the cancer cells,

wherein the activated antigen-specific CD8+cytotoxic T cells are autologous to the patient,

wherein the cancer is hepatocellular carcinoma, brain cancer, non-small cell lung cancer, or kidney cancer.

2. The method of claim 1 , wherein the composition further comprises an adjuvant.

3. The method of claim 2 , wherein the adjuvant is selected from the group consisting of anti-CD40 antibody, imiquimod, resiquimod, Granulocyte Macrophage Colony Stimulating Factor (GM-CSF), cyclophosphamide, Sunitinib, bevacizumab, interferon-alpha, interferon-beta, CpG oligonucleotides and derivatives, polyinosinic:polycytidylic acid (poly-(I:C)) and derivatives, RNA, sildenafil, particulate formulations with poly(lactide co-glycolide) (PLG), virosomes, interleukin (IL)-1, IL-2, IL-4, IL-7, IL-12, IL-13, IL-15, IL-21, and IL-23.

4. The method of claim 3 , wherein the adjuvant is IL-7.

5. The method of claim 3 , wherein the adjuvant is IL-15.

6. The method of claim 3 , wherein the adjuvant is IL-21.

7. The method of claim 1 , wherein the cancer is hepatocellular carcinoma.

8. The method of claim 1 , wherein the cancer is brain cancer.

9. The method of claim 1 , wherein the cancer is non-small cell lung cancer.

10. The method of claim 1 , wherein the cancer is kidney cancer.

11. A method of eliciting a CD8+cytotoxic T cell response in an HLA-A*24+patient who has cancer that presents at the cell surface a peptide consisting of the amino acid sequence of IYVTSIEQI (SEQ ID NO: 214), wherein the cancer cells overexpress a GABAA receptor theta subunit (GABRQ) polypeptide comprising the amino acid sequence of IYVTSIEQI (SEQ ID NO: 214) as compared to a panel of normal tissues, wherein the cancer cells present at the cell surface a peptide consisting of the amino acid sequence of IYVTSIEQI (SEQ ID NO: 214) in a complex with HLA-A*24, comprising

administering to said patient who has cancer a composition comprising a population of activated antigen-specific CD8+cytotoxic T cells to kill the cancer cells in the patient,

wherein the population of the activated antigen-specific CD8+cytotoxic T cells recognize the cancer cells by interacting through their T cell receptor (TCR) with a peptide consisting of the amino acid sequence of IYVTSIEQI (SEQ ID NO: 214) in a complex with HLA-A*24 presented at the surface of the cancer cells,

wherein the activated antigen-specific CD8+cytotoxic T cells are autologous to the patient,

wherein the cancer is hepatocellular carcinoma, brain cancer, non-small cell lung cancer, or kidney cancer.

12. The method of claim 11 , wherein the composition further comprises an adjuvant.

13. The method of claim 12 , wherein the adjuvant is selected from the group consisting of anti-CD40 antibody, imiquimod, resiquimod, Granulocyte Macrophage Colony Stimulating Factor (GM-CSF), cyclophosphamide, Sunitinib, bevacizumab, interferon-alpha, interferon-beta, CpG oligonucleotides and derivatives, polyinosinic:polycytidylic acid (poly-(I:C)) and derivatives, RNA, sildenafil, particulate formulations with poly(lactide co-glycolide) (PLG), virosomes, interleukin (IL)-1, IL-2, IL-4, IL-7, IL-12, IL-13, IL-15, IL-21, and IL-23.

14. The method of claim 13 , wherein the adjuvant is IL-7.

15. The method of claim 13 , wherein the adjuvant is IL-15.

16. The method of claim 13 , wherein the adjuvant is IL-21.

17. The method of claim 11 , wherein the cancer is hepatocellular carcinoma.

18. The method of claim 11 , wherein the cancer is brain cancer.

19. The method of claim 11 , wherein the cancer is non-small cell lung cancer.

20. The method of claim 11 , wherein the cancer is kidney cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2022
From: WEINSCHENK, TONI; MAHR, ANDREA; FRITSCHE, JENS; MUELLER, PHILLIP; WIEBE, ANITA; KUTSCHER, SARAH
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 060357/0672 →
Priority Claims (2)
GB 1423016 · Dec 23, 2014 · national
GB 1501017 · Jan 21, 2015 · national
Continuity (6)
Continuation 17728756 · Apr 25, 2022
Continuation 15918788 · Mar 12, 2018
Continuation 15357757 · Nov 21, 2016
Continuation 14975952 · Dec 21, 2015
Provisional Application 62096165 · Dec 23, 2014
Related Publication 20230031307A1 · Feb 2, 2023