Novel peptides and combination of peptides for use in immunotherapy against lung cancer, including nsclc, sclc and other cancers

a technology of immunotherapy and peptides, applied in the field of peptides, proteins, nucleic acids and cells for use in immunotherapy of cancer, can solve the problems of poor prognosis, poor survival rate for all stages combined, and inability to isolate class ii peptides directly from primary tumors, etc., and achieve high error rates.

Inactive Publication Date: 2019-03-28
IMMATICS BIOTECHNOLOGIES GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0040]The following tables show the peptides according to the present invention, their respective SEQ ID NOs, and the prospective source (underlying) genes for these peptides. In Table 1, peptides with SEQ ID NO: 1 to SEQ ID NO: 83 bind to HLA-A*24, peptides with SEQ ID NO: 84 to SEQ ID NO: 133 bind to HLA-A*02, peptides with SEQ ID NO: 134 to SEQ ID NO: 201 bind to HLA-A*01, peptides with SEQ ID NO: 202 to SEQ ID NO: 219 bind to HLA-A*03, peptides with SEQ ID NO: 220 to SEQ ID NO: 295 bind to HLA-B*07, peptides with SEQ ID NO: 296 to SEQ ID NO: 318 bind to HLA-B*08, peptides with SEQ ID NO: 319 to SEQ ID NO: 374 bind to HLA-B*44. The peptides in Table 2 have been disclosed before in large listings as results of high-throughput screenings with high error rates or calculated using algorithms, but have not ...

Problems solved by technology

Prognosis is generally poor.
However, the 5-year survival rate for all stages combined is only 17%.
Since the constitutive expression of HLA class II molecules is usually limited to immune cells, the possibility of isolating class II peptides directly from primary tumors was previously not ...

Method used

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  • Novel peptides and combination of peptides for use in immunotherapy against lung cancer, including nsclc, sclc and other cancers
  • Novel peptides and combination of peptides for use in immunotherapy against lung cancer, including nsclc, sclc and other cancers
  • Novel peptides and combination of peptides for use in immunotherapy against lung cancer, including nsclc, sclc and other cancers

Examples

Experimental program
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Effect test

example 1

[0343]Identification and Quantitation of Tumor Associated Peptides Presented on the Cell Surface

[0344]Tissue Samples

[0345]Patients' tumor tissues were obtained from: Asterand (Detroit, Mich., USA & Royston, Herts, UK); Bio-Options Inc. (Brea, Calif., USA); Geneticist Inc. (Glendale, Calif., USA); University Hospital Heidelberg (Heidelberg, Germany); ProteoGenex Inc. (Culver City, Calif., USA); Tissue Solutions Ltd (Glasgow, UK); University Hospital Munich (Munich, Germany). Normal tissues were obtained from Asterand (Detroit, Mich., USA & Royston, Herts, UK); Bio-Options Inc. (Brea, Calif., USA); BioServe (Beltsville, Md., USA); Capital BioScience Inc. (Rockville, Md., USA); Centre for Clinical Transfusion Medicine Tuebingen (Tübingen, Germany); Geneticist Inc. (Glendale, Calif., USA); Kyoto Prefectural University of Medicine (KPUM) (Kyoto, Japan); Osaka City University (OCU) (Osaka, Japan); ProteoGenex Inc. (Culver City, Calif., USA); Tissue Solutions Ltd (Glasgow, UK); University ...

example 2

[0352]Expression Profiling of Genes Encoding the Peptides of the Invention

[0353]Over-presentation or specific presentation of a peptide on tumor cells compared to normal cells is sufficient for its usefulness in immunotherapy, and some peptides are tumor-specific despite their source protein occurring also in normal tissues. Still, mRNA expression profiling adds an additional level of safety in selection of peptide targets for immunotherapies. Especially for therapeutic options with high safety risks, such as affinity-matured TCRs, the ideal target peptide will be derived from a protein that is unique to the tumor and not found on normal tissues.

[0354]RNA Sources and Preparation

[0355]Surgically removed tissue specimens were provided as indicated above (see Example 1) after written informed consent had been obtained from each patient. Tumor tissue specimens were snap-frozen immediately after surgery and later homogenized with mortar and pestle under liquid nitrogen. Total RNA was pre...

example 3

[0362]In Vitro Immunogenicity for MHC Class I Presented Peptides

[0363]In order to obtain information regarding the immunogenicity of the TUMAPs of the present invention, the inventors performed investigations using an in vitro T-cell priming assay based on repeated stimulations of CD8+ T cells with artificial antigen presenting cells (aAPCs) loaded with peptide / MHC complexes and anti-CD28 antibody. This way the inventors could show immunogenicity for HLA-A*02:01, HLA-A*24:02, HLA-A*01:01, HLA-A*03:01, HLA-B*07:02, HLA-B*08:01 and HLA-B*44:02 restricted TUMAPs of the invention, demonstrating that these peptides are T-cell epitopes against which CD8+ precursor T cells exist in humans (Table 10a and Table 10b).

[0364]In Vitro Priming of CD8+ T Cells

[0365]In order to perform in vitro stimulations by artificial antigen presenting cells loaded with peptide-MHC complex (pMHC) and anti-CD28 antibody, the inventors first isolated CD8+ T cells from fresh HLA-A*02, HLA-A*24, HLA-A*01, HLA-A*03,...

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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.

Description

CROSS REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of U.S. patent application Ser. No. 16 / 026,707, filed 3 Jul. 2018, which is related to PCT / EP2018 / 067979 filed 3 Jul. 2018 and claims priority to U.S. Provisional Application No. 62 / 529,758 filed 7 Jul. 2017, and German Patent Application No. 102017115301.2, filed 7 Jul. 2017, the content of each is hereby incorporated by reference.REFERENCE TO SEQUENCE LISTING SUBMITTED AS A COMPLIANT ASCII TEXT FILE (.txt)[0002]Pursuant to the EFS-Web legal framework and 37 CFR §§ 1.821-825 (see MPEP § 2442.03(a)), a Sequence Listing in the form of an ASCII-compliant text file (entitled “Sequence_Listing_2912919-089002_ST25.txt” created on 6 Dec. 2018, and 83,090 bytes in size) is submitted concurrently with the instant application, and the entire contents of the Sequence Listing are incorporated herein by reference.BACKGROUND[0003]The present invention relates to peptides, proteins, nucleic acids and cells for use in ...

Claims

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Application Information

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IPC IPC(8): C07K14/47A61K39/00C12N15/115C12N15/10C07K14/74C07K14/725C07K16/30G01N33/574C12N5/0783
CPCC12N2501/50G01N33/57492A61K2039/572C12N5/0638C07K14/4748A61K39/001102C07K16/30C07K14/7051C07K14/70539C12N15/1062C12N15/115C07K2319/00A61K39/0011A61K2039/5158A61P35/00C07K16/2818A61K35/17A61K38/00C07K7/06C07K14/5434
Inventor SONG, COLETTESCHOOR, OLIVERFRITSCHE, JENSWEINSCHENK, TONISINGH, HARPREET
Owner IMMATICS BIOTECHNOLOGIES GMBH
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