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Monoclonal antigen-binding proteins to intracellular oncogene products

a technology of monoclonal antibodies and oncogene products, applied in the field of chimeric antigen receptors, recombinant antibodies, etc., can solve the problems of difficult to make a drug selective for ras proteins, and the availability of traditional antibody-based strategies targeting cell surface antigens

Active Publication Date: 2021-10-28
MEMORIAL SLOAN KETTERING CANCER CENT +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present patent is about identifying and characterizing antibodies that can target cytosolic / intracellular proteins, such as the Ras oncoprotein. The antibodies can recognize and bind to peptides that are presented on the surface of cells by MHC antigens. The antibodies can be used to generate antigen-binding proteins that can be used to target specific mutations of the Ras protein. The technical effect of this patent is the ability to generate antibodies that can recognize and bind to peptides that are presented on the surface of cells by MHC antigens.

Problems solved by technology

However, because the mutant Ras that is associated with cancers is so similar to the normal Ras protein found in all human cells, (the mutant differing by a single amino acid,) and because Ras's oncogenic function is not a mutated enzyme targetable by a small molecule in the traditional sense, it has been difficult to make a drug selective for Ras proteins.
No drug for Ras is FDA approved for human use.
But, unlike small molecule drugs that cross the cell membrane, mAbs cannot cross the membrane to access intracellular proteins like Ras and therefore, traditional antibody-based strategies targeting cell surface antigens are unavailable.

Method used

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  • Monoclonal antigen-binding proteins to intracellular oncogene products
  • Monoclonal antigen-binding proteins to intracellular oncogene products
  • Monoclonal antigen-binding proteins to intracellular oncogene products

Examples

Experimental program
Comparison scheme
Effect test

example 1

Epitope Selection and Peptide Synthesis

[0078]For purposes of the present disclosure, K-Ras peptides are identified by amino acid position(s) relative to NCBI Reference Sequence NP_203524.1 of the NCBI protein database. Accordingly, the K-Ras peptides, LWVGAGGV and KLVVVGAGGV correspond to amino acids 6-14 and 5-14, respectively, of the reference sequence.

[0079]In order to select HLA-A2-restricted epitopes derived from Ras codon 12-mutations with strong immunogenicity, the prediction scores of Ras mutation sequences were first screened using three online available databases (BIMAS, RANKPEP and SYFPEITHI). (Ras mutation sequences are described in Smith et al. Oncogenic mutations in ras create HLA-A2.1 binding peptides but affect their extracellular antigen processing. International Immunology Vol. 9(8), pp. 1085-1093, 1997).

[0080]Based on the predicted binding scores from all three databases, the following peptides were selected for testing to determine if the peptides were able to el...

example 2

T2 Stabilization Assay

[0084]The immunogenicity of MHC class I-restricted peptides requires the capacity to bind and stabilize MHC class I molecules on the live cell surface. Moreover, the computer prediction has only up to 70% accuracy; so the next step was to seek a direct measurement of the strength of the interaction between the peptides and the HLA-A0201 molecules using a conventional binding and stabilization assay that uses antigen-transporting-deficient (TAP2 negative) HLA-A0201 human T2 cells. T2 cells lack TAP function and consequently are defective in properly loading class I molecules with antigenic peptides generated in the cytosol. The association of exogenously added peptides with thermolabile, empty HLA-A0201 molecules stabilizes them and results in an increase in the level of surface HLA-A0201 recognizable by a specific anti-HLA-A0201 mAb such as BB7.2.

[0085]The T2 binding assay showed that Ras 10-mer peptides wild type (WT), G12V, G12C, G12D increased the HLA-A2 exp...

example 3

Mutant Ras Peptide-Induced T Cell Responses

[0086]After informed consent on Memorial Sloan-Kettering Cancer Center Institutional Review Board approved protocols, peripheral blood mononuclear cells (PBMCs) from HLA-typed healthy donors were obtained by Ficoll density centrifugation. T cell stimulation followed the protocol described previously (Dao T. et al. Identification of a human cyclin D1-derived peptide that induces human cytotoxic CD4 cells. Plos One Vol. 4(9) e6730, 2009). Peptide-specific T cell responses were measured by IFN-g ELISPOT assay (Dao, T, Science Tr Med 2013).

[0087]To expand the peptide-specific T cell precursors, three to five in vitro stimulations were performed and the specific T cell response was measured by IFN-g production, when challenged with individual peptide. Ras-G12V peptide stimulation induced strong T cell response against Ras10-G12V but showed no cross-reactivity to the peptides Ras10-WT, G12C and G12D (FIG. 2A). Similarly, Ras 9-G12V also induced s...

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Abstract

Antigen binding proteins specific for an HLA-A2 restricted Ras peptide are disclosed. The antigen binding proteins encompass antibodies in a variety of forms, including full-length antibodies, substantially intact antibodies, Fab fragments, F(ab′)2 fragments, and single chain Fv fragments. Fusion proteins, such as scFv fusions with immunoglobulin or T-cell receptor domains, and bispecific antibodies incorporating the specificity of the antigen binding region for each peptide are also contemplated by the disclosure. Furthermore, immunoconjugates may include antibodies to which is linked a radioisotope, fluorescent or other detectable marker, cytotoxin, or other molecule are also encompassed by the disclosure. Among other things, immunoconjugates can be used for delivery of an agent to elicit a therapeutic effect or to facilitate an immune effector function.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of PCT / US2016 / 023247 filed on Mar. 18, 2016 which published as WO 2016 / 154047 on Sep. 29, 2016, and which claims the priority of U.S. Provisional Application No. 62 / 136,117, filed Mar. 20, 2015; the entire contents of each are hereby incorporated in their entirety into the present disclosure.SEQUENCE LISTING[0002]The instant application contains a Sequence Listing, created on Mar. 18, 2015; the file, in ASCII format, is designated 3314061AWO_ST25.txt and is 77.8 kilobytes in size. The file is hereby incorporated by reference in its entirety into the instant application.BACKGROUND OF THE DISCLOSURETechnical Field[0003]The present disclosure relates generally to antigen-binding protein molecules involved in immune function. More particularly, the present disclosure relates to recombinant antibodies, chimeric antigen receptors and fragments or portions thereof with binding specificity for Ras proteins.Backg...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07K16/40A61K47/68C07K16/28
CPCC07K16/40C07K2319/70C07K16/2809C07K2317/34C07K2317/56C07K2317/565C07K2317/21C07K2317/567C07K2317/92C07K2317/55C07K2317/14C07K2317/31C07K2317/54C07K2317/732C07K2317/622A61K47/6871A61K39/0011
Inventor SCHEINBERG, DAVID A.DAO, TAOLIU, CHENG
Owner MEMORIAL SLOAN KETTERING CANCER CENT
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