IP Library › Granted Patent US 11,793,866
Granted Patent B2
US 11,793,866 · App. 17/320,763 · Granted Oct 24, 2023

Peptides and T cells for use in immunotherapeutic treatment of various cancers

Inventors: Andrea Mahr (Tuebingen, DE); Toni Weinschenk (Aichwald, DE); Oliver Schoor (Tuebingen, DE); Jens Fritsche (Dusslingen, DE); Harpreet Singh (Munich, DE)
Assignee: IMMATICS BIOTECHNOLOGIES GMBH
A61K39/0011A61P35/00C07K7/06C07K7/08C07K14/4748C07K14/7051C07K14/70539C07K16/2833C07K16/3076C12N5/0636C12N15/115C12Q1/6886G01N33/57492A61K39/00A61K2039/5158C07K2319/40C12N2310/16C12N2501/50C12Q2600/106C12Q2600/156G01N2333/70539
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Quick Facts
Patent No.
US 11,793,866
App. No.
17/320,763
Granted
Oct 24, 2023
Kind
B2
Abstract

The present invention relates to peptides, proteins, nucleic acids and cells for use in immunotherapeutic methods. In particular, the present invention relates to the immunotherapy of cancer. The present invention furthermore relates to tumor-associated T-cell peptide epitopes, alone or in combination with other tumor-associated peptides that can for example serve as active pharmaceutical ingredients of vaccine compositions that stimulate anti-tumor immune responses, or to stimulate T cells ex vivo and transfer into patients. Peptides bound to molecules of the major histocompatibility complex (MHC), or peptides as such, can also be targets of antibodies, soluble T-cell receptors, and other binding molecules.

Claims (20)

1. A peptide consisting of the amino acid sequence ILSVVNSQL (SEQ ID NO: 323) in the form of a pharmaceutically acceptable salt.

2. The peptide of claim 1 , wherein said peptide has the ability to bind to an MHC class-I molecule, and wherein said peptide, when bound to said MHC, is capable of being recognized by CD8 T cells.

3. The peptide of claim 1 , wherein the pharmaceutically acceptable salt is chloride salt.

4. The peptide of claim 1 , wherein the pharmaceutically acceptable salt is acetate salt.

5. A composition comprising the peptide of claim 1 , wherein the composition comprises an adjuvant and a pharmaceutically acceptable carrier.

6. The composition of claim 5 , wherein the peptide is in the form of a chloride salt.

7. The composition of claim 5 , wherein the peptide is in the form of an acetate salt.

8. The composition of claim 5 wherein the adjuvant is selected from the group consisting of anti-CD40 antibody, imiquimod, resiquimod, GM-CSF, cyclophosphamide, sunitinib, bevacizumab, interferon-alpha, interferon-beta, CpG oligonucleotides and derivatives, 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.

9. The composition of claim 8 , wherein the adjuvant is IL-2.

10. The composition of claim 8 , wherein the adjuvant is IL-7.

11. The composition of claim 8 , wherein the adjuvant is IL-12.

12. The composition of claim 8 , wherein the adjuvant is IL-15.

13. The composition of claim 8 , wherein the adjuvant is IL-21.

14. A pegylated peptide consisting of the amino acid sequence of ILSVVNSQL (SEQ ID NO: 323) or a pharmaceutically acceptable salt thereof.

15. The peptide of claim 14 , wherein the pharmaceutically acceptable salt is chloride salt.

16. The peptide of claim 14 , wherein the pharmaceutically acceptable salt is acetate salt.

17. A composition comprising the pegylated peptide of claim 14 or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

18. A peptide consisting of the amino acid sequence of ILSVVNSQL (SEQ ID NO: 323), wherein at least one amino acid of the peptide is a D-amino acid.

19. The peptide in the form of a pharmaceutically acceptable salt of claim 1 , wherein said peptide is produced by solid phase peptide synthesis or produced by a yeast cell or bacterial cell expression system.

20. A composition comprising the peptide of claim 1 , wherein the composition is a pharmaceutical composition and comprises water and a buffer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2021
From: MAHR, ANDREA; WEINSCHENK, TONI; SCHOOR, OLIVER; FRITSCHE, JENS; SINGH, HARPREET
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 056247/0069 →
Priority Claims (1)
GB 1515321 · Aug 28, 2015 · national
Continuity (7)
Continuation 17017358 · Sep 10, 2020
Continuation 16887765 · May 29, 2020
Continuation 16673619 · Nov 4, 2019
Continuation 15982293 · May 17, 2018
Continuation 15249083 · Aug 26, 2016
Provisional Application 62211276 · Aug 28, 2015
Related Publication 20220331413A1 · Oct 20, 2022