IP Library › Granted Patent US 10,934,333
Granted Patent B2
US 10,934,333 · App. 16/915,745 · Granted Mar 2, 2021

Peptides and combination of peptides for use in immunotherapy against ovarian cancer and other cancers

Inventors: Andrea Mahr (Tuebingen, DE); Toni Weinschenk (Aichwald, DE); Helen Hoerzer (Tuebingen, DE); Oliver Schoor (Tuebingen, DE); Jens Fritsche (Dusslingen, DE); Harpreet Singh (Munich, DE)
Assignee: IMMATICS BIOTECHNOLOGIES GMBH
C07K14/4748A61K35/17A61K39/0011C07K7/06C07K7/08C07K14/4705C07K14/4738C07K14/705C07K14/70539C07K14/82C07K16/18C07K16/28C07K16/2833C07K16/30C07K16/303C07K16/3015C07K16/3023C07K16/3038C07K16/3046C07K16/3053C07K16/3069C07K16/32C12N5/0636C12N15/115C12P21/02C12Q1/6881C12Q1/6886G01N33/56977G01N33/57449G01N33/57492A61K38/00A61K39/00A61K2035/124A61K2039/5158C07K2317/24C07K2317/31C07K2317/34C07K2319/00C07K2319/40C12N2310/16C12N2320/30C12N2501/50C12N2501/998C12Q2600/158G01N2333/70539
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Quick Facts
Patent No.
US 10,934,333
App. No.
16/915,745
Granted
Mar 2, 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 (20)

1. A method of treating a patient who has cancer, comprising administering to said patient a composition comprising a population of activated T cells that kill cancer cells in the patient that express a peptide, wherein said peptide consists of the amino acid sequence of SVQGEDLYLV (SEQ ID NO: 406), wherein said cancer is ovarian cancer, liver cancer, or uterine cancer.

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 T cells are derived from tumor infiltrating lymphocytes or peripheral blood mononuclear cells.

5. The method of claim 1 , wherein the peptide is in a complex with an MHC molecule.

6. The method of claim 1 , wherein the composition further comprises an adjuvant 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, and particulate formations 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.

7. The method of claim 6 , wherein the adjuvant is IL-2.

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

9. The method of claim 1 , wherein the activated T cells are cytotoxic T cells produced by contacting T cells with an antigen presenting cell that presents the peptide in a complex with an MHC class I molecule on the surface of the antigen presenting cell, for a period of time sufficient to activate said T cell specifically against the peptide.

10. The method of claim 9 , wherein the antigen presenting cell is infected with a recombinant virus expressing the peptide.

11. The method of claim 1 , wherein the cancer is ovarian cancer.

12. The method of claim 1 , wherein the cancer is liver cancer.

13. The method of claim 1 , wherein the cancer is uterine cancer.

14. A method of eliciting an immune response in a patient who has ovarian cancer, liver cancer, or uterine cancer, comprising administering to said patient a composition comprising a peptide in the form of a pharmaceutically acceptable salt and an adjuvant, wherein said peptide consists of the amino acid sequence of SVQGEDLYLV (SEQ ID NO: 4061 thereby inducing a T-cell response to the ovarian cancer, liver cancer, or uterine cancer.

15. The method of claim 14 , wherein the T cell response is a cytotoxic T cell response.

16. The method of claim 14 , 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.

17. The method of claim 14 , wherein the immune response is capable of killing cancer cells that present a peptide consisting of the amino acid sequence of SVQGEDLYLV (SEQ ID NO: 406.

18. The method of claim 14 , wherein the cancer is ovarian cancer.

19. The method of claim 14 , wherein the cancer is liver cancer.

20. The method of claim 14 , wherein the cancer is uterine cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2020
From: MAHR, ANDREA; WEINSCHENK, TONI; HOERZER, HELEN; SCHOOR, OLIVER; FRITSCHE, JENS; SINGH, HARPREET
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 053078/0565 →
Priority Claims (1)
GB 1511546 · Jul 1, 2015 · national
Continuity (5)
Continuation 16889352 · Jun 1, 2020
Continuation 15815644 · Nov 16, 2017
Continuation 15199199 · Jun 30, 2016
Provisional Application 62187507 · Jul 1, 2015
Related Publication 20200325194A1 · Oct 15, 2020
Cited By (1)
US 12,466,878