IP Library Granted Patent US 10,105,428
Granted Patent B2
US 10,105,428 · App. 15/799,495 · Granted Oct 23, 2018

Peptides and combination of peptides and scaffolds for use in immunotherapy against renal cell carcinoma (RCC) and other cancers

Inventors: Andrea Mahr (Tuebingen, DE); Toni Weinschenk (Aichwald, DE); Oliver Schoor (Tübingen, DE); Jens Fritsche (Dusslingen, DE); Harpreet Singh (Houston, TX); Colette Song (Ostfildern, DE)
Assignee: IMMATICS BIOTECHNOLOGIES GMBH
A61K39/0011A61K35/17C07K14/4748C07K14/70539C07K16/18C07K16/2833C07K16/3038C12N5/0636C12N15/115G06F19/20A61K2035/124A61K2039/505A61K2039/5158A61K2039/572C07K14/705C07K2317/73C07K2317/76C07K2319/33C07K2319/55C12N2310/16
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Quick Facts
Patent No.
US 10,105,428
App. No.
15/799,495
Granted
Oct 23, 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 (23)

1. A method of treating a patient who has cancer, comprising

administering to said patient a population of activated T cells that selectively recognize cells that aberrantly express a peptide consisting of the amino acid sequence of ALDPSGNQLI (SEQ ID NO: 12),

wherein said cancer is selected from the group consisting of kidney cancer (RCC), lung cancer, brain cancer, stomach cancer, colon or rectal cancer, liver cancer, pancreatic cancer, prostate cancer, leukemias, breast cancer, melanoma, ovarian cancer, and esophageal 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 activated T cells are expanded in vitro.

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

7. The method of claim 6 , wherein the composition further comprises an adjuvant.

8. The method of claim 7 , wherein the adjuvant is selected from the group consisting of imiquimod, resiguimod, GM-CSF, cyclophosphamide, Sunitinib, bevacizumab, interferon-alpha, CpG oligonucleotides and derivatives, poly-(I:C) and derivatives, RNA, sildenafil, and particulate formations with poly(lactid coglycolid) (PLG) and virosomes.

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 expresses the peptide in a complex with an WIC class I molecule on the surface of the antigen presenting cell, for a period of time sufficient to activate said T cell.

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 10 , wherein the antigen presenting cell is a dendritic cell or a macrophage.

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

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

14. The method of claim 9 , wherein the contacting is in vitro.

15. The method of claim 1 , wherein the cancer is kidney cancer (RCC).

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

17. A method of treating a patient who has kidney cancer (RCC), lung cancer, brain cancer, stomach cancer, colon or rectal cancer, liver cancer, pancreatic cancer, prostate cancer, leukemias, breast cancer, melanoma, ovarian cancer, and/or esophageal 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 ALDPSGNQLI (SEQ ID NO: 12), thereby inducing a T-cell response to the kidney cancer (RCC), lung cancer, brain cancer, stomach cancer, colon or rectal cancer, liver cancer, pancreatic cancer, prostate cancer, leukemias, breast cancer, melanoma, ovarian cancer, and/or esophageal cancer.

18. The method of claim 17 , wherein the T cell response is a cytotoxic T cell response.

19. The method of claim 17 , wherein the cancer is kidney cancer (RCC).

20. The method of claim 17 , wherein the cancer is ovarian cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 1, 2017
From: MAHR, ANDREA; WEINSCHENK, TONI; SCHOOR, OLIVER; FRITSCHE, JENS; SINGH, HARPREET; SONG, COLETTE
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 044275/0219 →
Continuity (3)
Continuation 15082920 · Mar 28, 2016
Provisional Application 62140767 · Mar 31, 2015
Related Publication 20180064796A1 · Mar 8, 2018
Cited By (1)
US 12,466,878