IP Library › Granted Patent US 10,898,557
Granted Patent B2
US 10,898,557 · App. 16/887,765 · Granted Jan 26, 2021

Method of treating with a peptide

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 10,898,557
App. No.
16/887,765
Granted
Jan 26, 2021
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 (28)

1. A method for treating a patient who has cancer, comprising administering to the patient a population of activated T cells that kill cancer cells that present a peptide consisting of the amino acid sequence of SEQ ID NO: 244,

wherein the peptide is in a complex with an MHC molecule,

wherein said cancer is non-small cell lung cancer, esophageal cancer, or head-and neck squamous cell carcinoma.

2. The method of claim 1 , wherein the T cells are autologous to the patient.

3. The method of claim 1 , wherein the T cells are obtained from a healthy donor.

4. The method of claim 1 , wherein the activated T cells are produced by contacting T cells with the peptide loaded human class I or II MHC molecules expressed on the surface of an antigen-presenting cell for a period of time sufficient to activate the T cells.

5. The method of claim 1 , wherein the activated T cells are expanded in vitro.

6. The method of claim 1 , wherein the peptide is in a complex with the class I MHC molecule.

7. The method of claim 4 , wherein the antigen presenting cell is infected with a recombinant virus expressing the peptide.

8. The method of claim 7 , wherein the antigen presenting cell is a dendritic cell or a macrophage.

9. The method of claim 5 , wherein the expansion is in the presence of an anti-CD28 antibody and IL-12.

10. The method of claim 1 , wherein the population of activated T cells comprises CD8-positive cells.

11. The method of claim 4 , wherein the contacting is in vitro.

12. The method of claim 1 , wherein the population of activated T cells are administered in the form of a composition.

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

14. The method of claim 13 , 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.

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

16. A method of eliciting an immune response in a patient who has cancer comprising administering to the patient a population of activated T cells that selectively recognize cancer cells that present a peptide consisting of the amino acid sequence of SEQ ID NO: 244,

wherein the peptide is in a complex with an MEW molecule,

wherein said cancer is non-small cell lung cancer, esophageal cancer, or head-and neck squamous cell carcinoma.

17. The method of claim 16 , wherein the T cells are autologous to the patient.

18. The method of claim 16 , wherein the T cells are obtained from a healthy donor.

19. The method of claim 16 , wherein the activated T cells are produced by contacting T cells with the peptide loaded human class I or II MHC molecules expressed on the surface of an antigen-presenting cell for a period of time sufficient to activate the T cells.

20. The method of claim 16 , wherein the cancer is non-small cell lung cancer.

21. The method of claim 16 , wherein the cancer is esophageal cancer.

22. The method of claim 16 , wherein the cancer is head-and neck squamous cell carcinoma.

23. The method of claim 1 , wherein the cancer is esophageal cancer.

24. The method of claim 1 , wherein the cancer is head-and neck squamous cell carcinoma.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2020
From: MAHR, ANDREA; WEINSCHENK, TONI; SCHOOR, OLIVER; FRITSCHE, JENS; SINGH, HARPREET
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 052791/0616 →
Priority Claims (1)
GB 1515321.6 · Aug 28, 2015 · national
Continuity (5)
Continuation 16673619 · Nov 4, 2019
Continuation 15982293 · May 17, 2018
Continuation 15249083 · Aug 26, 2016
Provisional Application 62211276 · Aug 28, 2015
Related Publication 20200289631A1 · Sep 17, 2020