US2019010190A1PendingUtilityA1

Novel immunotherapy against several tumors including neuronal and brain tumors

Assignee: IMMATICS BIOTECHNOLOGIES GMBHPriority: Oct 1, 2008Filed: Sep 19, 2018Published: Jan 10, 2019
Est. expiryOct 1, 2028(~2.2 yrs left)· nominal 20-yr term from priority
A61P 35/00A61P 35/02A61P 37/04A61P 25/00A61P 27/02A61P 17/00A61P 11/00A61P 1/04A61P 15/00A61P 1/18A61P 13/08A61P 13/12G01N 33/5759C07K 2319/00C12N 2501/50A61K 2039/55561A61K 2039/53A61K 38/00C07K 2319/40A61K 2039/572A61M 5/002A61K 38/16A61K 2039/55516A61K 2039/605C07K 7/06C07K 7/08A61K 2039/6093C07K 14/70539A61K 2039/55522A61K 2039/55588A61K 2039/6081A61K 2039/55511A61K 38/08A61K 2039/5158Y02A50/472C12N 5/0638A61K 35/17A61K 39/0011G01N 33/57492A61K 2039/5154A61K 40/42A61K 40/11C07K 7/00C12N 5/0639A61K 39/00Y02A50/30A61K 39/001102
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Claims

Abstract

The present invention relates to peptides, 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 cytotoxic T cell (CTL) peptide epitopes, alone or in combination with other tumor-associated peptides that serve as active pharmaceutical ingredients of vaccine compositions that stimulate anti-tumor immune responses. The present invention relates to 30 peptide sequences and their variants derived from HLA class I and class II molecules of human tumor cells that can be used in vaccine compositions for eliciting anti-tumor immune responses.

Claims

exact text as granted — not AI-modified
1 . A method of treating a patient who has cancer, comprising administering to the patient an effective amount of an antibody specifically binding to an MHC class I or II molecule complexed with a HLA-restricted antigen consisting of the amino acid sequence of KIQEILTQV (SEO ID NO: 14), wherein the cancer is selected from the group consisting of glioblastoma, renal cell carcinoma, melanoma, endometrial cancer, esophageal squamous cell carcinoma, pancreatic cancer, and urothelial cancer. 
     
     
         2 . The method of  claim 1 , wherein the antibody is a polyclonal antibody, a monoclonal antibody, or a chimeric antibody. 
     
     
         3 . The method of  claim 1 , wherein the antibody binds to the HLA-restricted antigen with a binding affinity of below 20 nanomolar. 
     
     
         4 . The method of  claim 1 , wherein the antibody binds to the MHC class I molecule complexed with the HLA-restricted antigen. 
     
     
         5 . The method of  claim 1 , wherein the antibody is humanized. 
     
     
         6 . The method of  claim 1 , wherein the effective amount of the antibody is from about 1 μg/kg to about 100 mg/kg of body weight per day. 
     
     
         7 . The method of  claim 1 , wherein the antibody is conjugated with a toxin. 
     
     
         8 . The method of  claim 7 , wherein the toxin is selected from the group consisting of diptheria toxin,  pseudomonas  exotoxin A, cholera toxin, and ricin toxin. 
     
     
         9 . A method of diagnosing cancer in a subject, comprising
 administering to the subject an antibody specifically binding to an MHC class I or II molecule complexed with a HLA-restricted antigen consisting of the amino acid sequence of KIQEILTQV (SEO ID NO: 14),
 wherein the antibody is labeled with a radionucleotide, 
   detecting the radionucleotide, and   localizing the cancer using immunoscintiography, wherein the cancer is selected from the group consisting of glioblastoma, renal cell carcinoma, melanoma, endometrial cancer, esophageal squamous cell carcinoma, pancreatic cancer, and urothelial cancer.   
     
     
         10 . The method of  claim 9 , wherein the antibody is a polyclonal antibody, a monoclonal antibody, or a chimeric antibody. 
     
     
         11 . The method of  claim 9 , wherein the antibody has an affinity value (Kd) of less than 1×10 μM. 
     
     
         12 . The method of  claim 9 , wherein the antibody binds to the MHC class I molecule complexed with the HLA-restricted antigen. 
     
     
         13 . The method of  claim 9 , wherein the antibody is humanized. 
     
     
         14 . The method of  claim 9 , wherein the radionucleotide is selected from the group consisting of  111 In,  99 Tc,  14 C,  131 I,  3 H,  32 P,  35 S. 
     
     
         15 . The method of  claim 9 , wherein the immunoscintiography is positron emission tomography (PET). 
     
     
         16 . The method of  claim 1 , wherein the cancer is glioblastoma. 
     
     
         17 . The method of  claim 9 , wherein the cancer is glioblastoma. 
     
     
         18 . A method for producing an antibody specifically binding to a human major histocompatibility complex (MHC) class I or II molecule complexed with an HLA-restricted antigen consisting of the amino acid sequence of KIQEILTQV (SEO ID NO: 14), comprising
 immunizing a genetically engineered non-human mammal comprising cells expressing said MHC class I or II molecule with a soluble form of an MHC class I or II molecule complexed with said HLA-restricted antigen,   isolating mRNA molecules from antibody producing cells of said non-human mammal,   producing a phage display library displaying protein molecules encoded by said mRNA molecules, and   isolating at least one phage from said phage display library,
 wherein said at least one phage displays said antibody specifically binding to said MHC class I or II molecule complexed with said HLA-restricted antigen. 
   
     
     
         19 . The method of  claim 1 , wherein the antibody is a polyclonal antibody, a monoclonal antibody, or a chimeric antibody. 
     
     
         20 . The method of  claim 1 , wherein the antibody binds to the HLA-restricted antigen with a binding affinity of below 20 nanomolar. 
     
     
         21 . The method of  claim 1 , wherein the antibody binds to the MHC class I molecule complexed with the HLA-restricted antigen. 
     
     
         22 . The method of  claim 1 , further comprising humanizing the antibody.

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