SNP Detection for Predicting IFN-B Immune Response

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Solution Overview

Problem

There is a need for a method to predict the ability of a patient to produce an Interferon B (IFN-B) dependent adaptive immune response, which is crucial for the efficacy of therapies like radiotherapy, as current methods can only evaluate serum IFN-B levels after treatment, making it difficult to personalize treatment approaches.

Innovation Solution

Detecting specific single nucleotide polymorphisms (SNPs) such as rs12553564 and those in high linkage disequilibrium with it, including rs12551341, rs2275888, and rs10811449, in a biological sample to predict the likelihood of an IFN-B dependent adaptive immune response, allowing for a rapid and cost-effective prediction of treatment efficacy.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If serum IFN-B levels are measured to evaluate treatment efficacy, then treatment effectiveness can be assessed, but the measurement can only be performed after treatment administration

Engineering Contradiction:
Improvetreatment efficacy evaluationVSAvoidtime delay in evaluation
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent applies preliminary action by detecting SNP genotypes (such as rs12553564) before treatment to predict IFN-B response capability in advance. This allows treatment selection to be based on predicted response rather than waiting for post-treatment measurement, thereby resolving the time delay contradiction while maintaining evaluation accuracy

Inventive Principle:
Principle #10Preliminary action

2Reliability

If personalized therapy approaches are implemented based on genetic prediction, then treatment effectiveness is improved, but additional genetic testing is required

Engineering Contradiction:
Improvepersonalized treatment effectivenessVSAvoidgenetic testing requirement
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent extracts and focuses on specific, limited SNP markers (such as rs12553564 and related SNPs in linkage disequilibrium) that are strongly associated with IFN-B response. By selecting only these critical genetic markers rather than performing comprehensive genomic analysis, the method achieves reliable personalized treatment prediction while minimizing testing complexity

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent changes the parameter of genetic analysis from comprehensive genome-wide screening to targeted detection of specific SNP alleles. This parameter change allows using simple allele-specific PCR or similar targeted methods instead of complex sequencing, thereby achieving reliable prediction with reduced technical complexity

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS20230348998A1Method for predicting the efficiency of a treatment stimulating an IFN-beta dependent adaptive immune response via detection of a single nucleotide polymorphism
Publication Date: 2023.11.02 COMMISSARIAT A LENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES
  • US20230348998A1 patent drawing
  • US20230348998A1 patent drawing
  • US20230348998A1 patent drawing

AI summary

The present invention relates to a method for predicting the efficiency of a treatment stimulating an IFN-β dependent adaptive immune response, comprising a step of detecting the rs12553564 single nucleotide polymorphism (SNP), or an SNP in high linkage disequilibrium with same, said SNP being selected from rs12551341, rs2275888, and rs10811449, in a biological sample of a subject in need thereof.