HLA tumor antigen peptides of class I and II for treating mammary/breast carcinomas

A method for determining pharmaceutically active human leukocyte antigen (HLA) tumor antigen peptides for use in treatment or prophylaxis of mammary/breast carcinomas or in a composition for use in the treatment or prophylaxis of mammary/breast carcinomas, in particular locally recurrent or metastatic breast carcinomas in a patient or group of patients suffering from or suspected of suffering from mammary/breast carcinoma, comprising a pharmacologically effective amount comprising 4 to 8 HLA tumor antigen peptides corresponding to major histocompatibility complex (MHC) class I complexes and at least 2 tumor antigen peptides corresponding to MHC class II complexes, characterized in that the HLA tumor antigen peptides are tumor-exclusive or tumor-associated HLA antigen peptides, in particular those associated with mammary/breast carcinomas, wherein the HLA tumor antigen peptides comprise sequences contained in the sequences SEQ ID NO:

• 13-SEQ ID NO:
• 26, SEQ ID NO:
• 28, SEQ ID NO:
• 29 and SEQ ID NO:
• 32-SEQ ID NO:
• 48, comprising monitoring a tissue resection of a patient or group of patients suffering from or suspected of suffering from mammary/breast cancer, the method comprising the following steps:
• (a) providing a tissue sample of the patient or group of patients, wherein cells of the tissue sample express class I and/or class II MHC complexes and present them on their surface, wherein said method step (a) of providing the tissue sample does not itself comprise any surgical intervention in the patient or one of the patients of the group of patients;
• (b) determining the following parameters using the provided tissue sample from step (a):
• i) the transcriptome of the tissue sample provided, and
• comparison with the transcriptome of a healthy tissue sample from the patient or group of patients to determine up- and/or down-regulated mRNA sequences that differ by a factor of 3 from a threshold in the healthy tissue sample;
• and
• ii) the specific HLA haplotype of the patient or patient group;
• and
• iii) the exome sequence of the tissue sample provided, and
• comparing the exome of the provided tissue sample with the exome of a healthy tissue sample or with a gene database of the patient or patient group to determine somatic mutations, and
• determining the HLA tumor antigen peptides that have somatic mutations and are up- or down-regulated relative to the healthy tissue sample, determined in step (i);
• and
• determining the HLA tumor antigen peptides associated with proliferation, invasiveness, angiogenesis, and an increase in cytokeratin production of a mammary/breast carcinoma;
• and
• iv) the ligandome to determine the tumor antigen peptides presented on the surface of the cells of the mammary/breast carcinoma determined in step (iii);
• and
• v) the specific binding affinity of the HLA tumor antigen peptides determined in step (iv) against the corresponding MHC complex of the cell of the breast cancer by means of a database and/or a ranking algorithm, and
• vi) the immunogenicity of the HLA tumor antigen peptides determined in step (iv) by means of an immunogenicity test, in particular by Western blot, enzyme-linked immunosorbent assay (ELISA) techniques, in particular by enzyme-linked immunospot assay (ELISPOT), atomic force microscopy (AFM) or immunodetection with microscopic analysis;
• (c) selecting HLA tumor antigen peptides that meet the criteria according to the parameters defined in step (b) and that are expressed in the cells of the provided tissue sample and presented on the surface of these cells;
• administering, based on the selection of HLA tumor antigen peptides, a pharmaceutical composition comprising each individual HLA antigen peptide in the composition at an absolute concentration to a patient or a specifically identified group of patients having at least one identical HLA allele for the treatment or prophylaxis of mammary/breast carcinomas.