Beta1,3′-Galactosyllactose-Enriched GOS for DON Immunotoxicity

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Solution Overview

Problem

Mycotoxins, particularly deoxynivalenol (DON), negatively impact the adaptive immune response in humans and animals, leading to a decrease in immune cell frequencies and vaccine-specific IgG production, posing a significant concern for infants and young children.

Innovation Solution

Administration of galacto-oligosaccharides enriched with beta1,3′-galactosyllactose, which are non-digestible and reach the large intestine intact, where they are fermented by the intestinal microbiota, helping to restore the frequency of immune cells and improve vaccination responsiveness.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If DON is present in the diet, then immune cell frequencies and vaccine-specific IgG production decrease, but adding GOS comprising beta3'-GL restores immune response

Engineering Contradiction:
Improveadaptive immune responseVSAvoidDON-induced immunotoxicity
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

GOS comprising beta3'-GL acts as an intermediary substance that mediates between DON exposure and the immune system. The oligosaccharides are fermented by intestinal microbiota to produce metabolites that indirectly protect immune cells from DON-induced toxicity, restoring Th1 cell frequencies and IFN-γ production without directly neutralizing DON

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The invention converts the harmful effect of DON exposure into a beneficial outcome by using GOS supplementation. The harmful DON-induced immune suppression is transformed into an opportunity for enhanced immune protection through the prebiotic effects of GOS, which stimulate beneficial microbiota that in turn protect against immunotoxicity

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

2Reliability

If GOS is administered to restore immune response, then Th1 cell frequency and IFN-γ production increase, but the mechanism involves complex microbiota fermentation

Engineering Contradiction:
ImproveTh1 immune responseVSAvoidbiological mechanism complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The immune system restoration is achieved through self-service mechanisms where GOS serves as a prebiotic that enables the intestinal microbiota to naturally produce protective metabolites. The complex biological system self-regulates to restore immune function without external intervention beyond the initial GOS administration

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

GOS is administered in advance to establish a protective microbiota state before DON exposure fully impacts the immune system. The preliminary prebiotic action of GOS primes the intestinal ecosystem to resist DON-induced immunotoxicity and maintain immune cell frequencies

Inventive Principle:
Principle #10Preliminary action

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Galacto-oligosaccharides with beta1,3′-galactosyllactose attenuate the adverse effects of DON on the adaptive immune response by increasing Tbet+ Th1 cells and B cells, thereby enhancing the immune system's ability to respond to vaccines.

Implementation Method 1

Administration of galacto-oligosaccharides enriched with beta1,3′-galactosyllactose, which are non-digestible and reach the large intestine intact, where they are fermented by the intestinal microbiota

Methodology Applied
Scientific EffectFermentation: Fermentation

Data Source

PatentUS20250332182A1Galactooligosaccharides for improving immune response
Publication Date: 2025.10.30 NV NUTRICIA
  • US20250332182A1 patent drawing

AI summary

The invention relates to the use of beta 1,3′-galactosyllactose for ameliorating the harmful effects of food contaminants on the adaptive immune response such as vaccination response or response to a pathogen.