Identifying Surface Antigens for Tumor Diagnosis

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for identifying tumor-associated antigens are limited by the use of immunoeffectors from patients with advanced cancer, leading to potential tolerization and loss of effective immune recognition specificities, and have not shown solid evidence of real action in clinical studies.

Innovation Solution

A strategy involving data mining of human protein and nucleic acid databases to identify cancer-specific antigens accessible on the cell surface, using high-throughput methodologies to evaluate genes for transmembrane domains, homology searches, and subsequent laboratory experiments to validate aberrant activation in tumors, combining bioinformatic and experimental approaches.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If immunoeffectors from patients with advanced cancer are used to identify tumor-associated antigens, then immune recognition specificities can be obtained, but tolerization occurs and effective immune recognition specificities are lost

Engineering Contradiction:
Improveimmune recognition specificityVSAvoideffective immune recognition
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

Instead of using immunoeffectors from patients with advanced cancer (conventional approach), the patent inverts the approach by using immunoeffectors from healthy individuals or patients with early-stage disease. This reversal avoids the tolerization problem that occurs in advanced cancer patients while still obtaining relevant immune recognition specificities against tumor-associated antigens.

Inventive Principle:
Principle #13The other way round (Inversion)

2Ease of manufacture

If classical therapeutic procedures are used, then treatment can be administered, but cancers remain leading causes of death despite exhaustive use

Engineering Contradiction:
Improvetreatment availabilityVSAvoidtherapeutic effectiveness
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent introduces tumor-associated antigens as intermediaries between the therapeutic agent and the patient's immune system. By identifying and utilizing specific tumor-associated antigens that are recognized by the immune system, the therapy mediates a targeted immune response against cancer cells, bridging the gap between conventional treatment and effective cancer elimination.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Adaptability or versatility

If tumor vaccines and antibody therapy are used, then immune system intervention can be enhanced, but recognition of tumor-specific antigens is required which is not always achieved

Engineering Contradiction:
Improveimmune system interventionVSAvoidtumor-specific antigen recognition
Core Design Contradiction:
Adaptability or versatilityVSMeasurement precision

Solution Approach 1:

The patent applies preliminary action by systematically identifying and characterizing tumor-associated antigens before implementing vaccine or antibody therapy. Through bioinformatic analysis, expression profiling, and immunological screening, the specific antigens are pre-identified and validated as targets, ensuring that subsequent therapeutic interventions are directed against proven tumor-specific or tumor-associated antigens.

Inventive Principle:
Principle #10Preliminary action

Data Source

PatentUS9533043B2Identification of surface-associated antigens for tumor diagnosis and therapy
Publication Date: 2017.01.03 BIONTECH SE
  • US9533043B2 patent drawing
  • US9533043B2 patent drawing
  • US9533043B2 patent drawing

AI summary

An isolated truncated desmoglein 4 (DSG4) polypeptide splice variant of the invention is characterized by an amino acid sequence that lacks a region encoded before exon 9 or beyond exon 10 of the DSG4 gene having the polynucleotide sequence of SEQ ID NO: 75. Also disclosed is a method of diagnosing a cancer, or monitoring the course thereof, in a patient. The method comprises detecting in a tissue sample of a patient the expression of a tumor-associated antigen comprising the extracellular domain of a DSG4 polypeptide encoded by a DSG4 gene having the polynucleotide sequence of SEQ ID NO: 75, or a truncated DSG4 polypeptide splice variant characterized by an amino acid sequence that lacks a region encoded before exon 9 or beyond exon 10 of the DSG4 gene.