US2023312680A1PendingUtilityA1

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

Assignee: IMMATICS BIOTECHNOLOGIES GMBHPriority: Jan 27, 2017Filed: Apr 7, 2023Published: Oct 5, 2023
Est. expiryJan 27, 2037(~10.5 yrs left)· nominal 20-yr term from priority
A61K 2039/892A61K 40/11A61K 40/42C07K 14/4748A61K 39/0011A61K 39/00C12Q 2600/156C07K 2317/34A61K 39/00117A61K 39/001166A61K 39/001163A61K 39/001162A61K 39/001152A61K 39/001149A61K 39/001138A61K 39/001102G16B 30/00C12Q 1/6886C07K 16/2833C07K 16/2818C07K 14/70539A61P 35/00C07K 14/705
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Claims

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

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating a patient who has cancer, comprising administering to said patient a population of activated T cells that kill cancer cells that present a peptide consisting of the amino acid sequence of SQSPSVSQL (SEQ ID NO: 74), wherein the cancer is selected from ovarian cancer and uterine and endometrial cancer. 
     
     
         2 . 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 MHC class I molecule on the surface of the antigen presenting cell, for a period of time sufficient to activate said T cell. 
     
     
         3 . The method of  claim 1 , further comprising administering to said patient an adjuvant selected from 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. 
     
     
         4 . The method of  claim 3 , wherein the adjuvant is IL-2. 
     
     
         5 . The method of  claim 3 , wherein the adjuvant is IL-7. 
     
     
         6 . The method of  claim 3 , wherein the adjuvant is IL-12. 
     
     
         7 . The method of  claim 3 , wherein the adjuvant is IL-15. 
     
     
         8 . The method of  claim 3 , wherein the adjuvant is IL-21. 
     
     
         9 . The method of  claim 1 , wherein the cancer is ovarian cancer. 
     
     
         10 . The method of  claim 1 , wherein the cancer is uterine and endometrial cancer. 
     
     
         11 . A method of eliciting an immune response in a patient who has cancer, comprising administering to said patient a population of activated T cells that kill cancer cells that present a peptide consisting of the amino acid sequence of SQSPSVSQL (SEQ ID NO: 74), wherein the cancer is selected from ovarian cancer and uterine and endometrial cancer. 
     
     
         12 . The method of  claim 11 , 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 MHC class I molecule on the surface of the antigen presenting cell, for a period of time sufficient to activate said T cell. 
     
     
         13 . The method of  claim 11 , further comprising administering to said patient an adjuvant selected from 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. 
     
     
         14 . The method of  claim 13 , wherein the adjuvant is IL-2. 
     
     
         15 . The method of  claim 13 , wherein the adjuvant is IL-7. 
     
     
         16 . The method of  claim 13 , wherein the adjuvant is IL-12. 
     
     
         17 . The method of  claim 13 , wherein the adjuvant is IL-15. 
     
     
         18 . The method of  claim 13 , wherein the adjuvant is IL-21. 
     
     
         19 . The method of  claim 11 , wherein the cancer is ovarian cancer. 
     
     
         20 . The method of  claim 11 , wherein the cancer is uterine and endometrial cancer.

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