IP Library Granted Patent US 9,932,384
Granted Patent B2
US 9,932,384 · App. 15/082,933 · Granted Apr 3, 2018

Peptides and combination of peptides for use in immunotherapy against various tumors

Inventors: Andrea Mahr (Tuebingen, DE); Toni Weinschenk (Aichwald, DE); Oliver Schoor (Tuebingen, DE); Jens Fritsche (Dusslingen, DE); Harpreet Singh (Munich, DE); Lea Stevermann (Tuebingen, DE)
Assignee: immatics biotechnologies GmbH
C07K14/70539A61K38/06A61K38/08A61K38/1774A61K39/0005A61K39/0011A61K45/06C07K7/02C07K7/06C07K14/001C07K14/47C07K14/4702C07K14/4748C07K14/7051C07K16/18C07K16/2833C07K16/30C12N5/0636C12N5/0638C12N9/6491C12Q1/6886G01N33/505G01N33/5088G01N33/566G01N33/56972G01N33/56977A61K2039/5158A61K2039/54A61K2039/57A61K2039/572A61K2039/585C07K2317/24C07K2317/31C07K2317/34C07K2319/00C07K2319/40C12N2501/998C12N2502/11C12Q2600/106C12Q2600/158C12Y304/24G01N2333/47G01N2333/7051G01N2333/70503G01N2333/70539G01N2500/10
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Quick Facts
Patent No.
US 9,932,384
App. No.
15/082,933
Granted
Apr 3, 2018
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 (7)

1. A peptide comprising the amino acid sequence of KVWSDVTPL (SEQ ID NO: 24) in the form of a pharmaceutical acceptable salt, wherein said peptide has an overall length of less than 30 amino acids.

2. The peptide according to claim 1 , wherein said peptide has the ability to bind to an MHC class-I or II molecule, and wherein said peptide, when bound to said MHC, is capable of being recognized by CD4 and/or CD8 T cells.

3. The peptide according to claim 1 , wherein the peptide consists of or consists essentially of the amino acid sequence of KVWSDVTPL (SEQ ID NO: 24) in the form of a pharmaceutical acceptable salt.

4. The peptide according to claim 1 , wherein said peptide is modified and/or includes non-peptide bonds.

5. The peptide according to claim 1 , wherein said peptide is part of a fusion protein, and wherein the fusion protein optionally comprises N-terminal amino acids of the HLA-DR antigen-associated invariant chain (Ii).

6. The peptide according to claim 1 , wherein said peptide has an overall length of from 9 to 15 amino acids.

7. The peptide according to claim 2 , wherein said peptide has an overall length of from 9 to 15 amino acids.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2018
From: MAHR, ANDREA; WEINSCHENK, TONI; SCHOOR, OLIVER; FRITSCHE, JENS; SINGH, HARPREET; STEVERMANN, LEA
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 046894/0548 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 26, 2016
From: MAHR, ANDREA; WEINSCHENK, TONI; SCHOOR, OLIVER; FRITSCHE, JENS; SINGH, HARPRETE; STEVERMANN, LEA
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 039258/0281 →
Continuity (2)
Provisional Application 62139189 · Mar 27, 2015
Related Publication 20160279214A1 · Sep 29, 2016