Secretory IgA Extraction from Intestinal Fluid for Feed Efficiency

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Solution Overview

Problem

There is no effective method to produce secretory IgA with diverse antigen binding activity for use as a supplement to treat related disorders, and current methods for its production are limited, particularly for use in animals, where the diversity of antigen binding activity increases with environmental exposure.

Innovation Solution

A food composition containing pasteurized intestinal secretory IgA from pig or cow intestinal luminal fluid or mucosa, with greater than 10% of the proteinaceous material being IgA, or unhydrolyzed dried intestinal mucosa, is used to increase growth rate, improve feed efficiency, and reduce gastrointestinal inflammation and infection risk, along with a process involving polyethylene glycol precipitation and purification for isolating and purifying secretory IgA.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If secretory IgA is produced using conventional methods (chemistry, recombinant microorganism fermentation, or stem cells), then production is possible, but the diversity of antigen binding activity is limited

Engineering Contradiction:
Improvediversity of antigen binding activityVSAvoidproduction method complexity
Core Design Contradiction:
Adaptability or versatilityVSEase of manufacture

Solution Approach 1:

The patent extracts secretory IgA directly from intestinal luminal fluid or mucosa of animals, bypassing the need for complex chemical synthesis, recombinant microorganism fermentation, or stem cell methods. This extraction approach naturally preserves the diverse antigen binding activity that develops through animal exposure to environmental antigens, while avoiding the complexity of artificial production methods.

Inventive Principle:
Principle #2Taking out (Extraction)

2Adaptability or versatility

If secretory IgA is collected from animals for use as dietary/oral supplement, then diverse antigen binding activity is achieved, but the cost effectiveness is reduced

Engineering Contradiction:
Improvediverse antigen binding activityVSAvoidcost effectiveness
Core Design Contradiction:
Adaptability or versatilityVSQuantity of substance

Solution Approach 1:

The patent utilizes animals that naturally produce secretory IgA in their intestinal luminal fluid as a self-service source. Rather than requiring expensive pharmaceutical-grade production methods, the approach collects IgA from the natural bodily secretions of healthy animals, making the therapy more cost-effective while maintaining diverse antigen binding activity.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent changes the concentration parameter by requiring greater than 10% of the proteinaceous material to be IgA, ensuring high potency in the collected preparation. This concentration threshold allows for effective therapeutic doses while maintaining cost-effectiveness through efficient collection and purification processes.

Inventive Principle:
Principle #35Parameter changes

3Adaptability or versatility

If intestinal luminal fluid or mucosa is used as source of secretory IgA, then diverse antigen binding activity is obtained, but purification complexity increases

Engineering Contradiction:
Improvediverse antigen binding activityVSAvoidpurification process complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent extracts secretory IgA from intestinal luminal fluid or mucosa using purification processes that isolate the IgA while removing other proteins and contaminants. The requirement that greater than 10% of the proteinaceous material be IgA ensures effective purification without requiring excessively complex multi-step processes.

Inventive Principle:
Principle #2Taking out (Extraction)

4Reliability

If pasteurization is applied to SIgA preparations, then effectiveness is enhanced, but processing time and energy consumption increase

Engineering Contradiction:
Improveeffectiveness of SIgA preparationVSAvoidenergy consumption during pasteurization
Core Design Contradiction:
ReliabilityVSUse of energy by stationary object

Solution Approach 1:

The patent applies pasteurization parameters (temperature, time, and pH conditions) to enhance the effectiveness of SIgA preparations. By optimizing these parameters, the process achieves reliable therapeutic效果 while minimizing energy consumption and processing time.

Inventive Principle:
Principle #35Parameter changes

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

The use of secretory IgA in animal feed compositions effectively increases growth rate, improves feed efficiency, reduces gastrointestinal inflammation, and decreases infection risk, with pasteurization enhancing the effectiveness of the SIgA preparations.

Implementation Method 1

treating the intestinal luminal fluid of a pig with polyethylene glycol having a molecular weight of 3000 to 30,000 to precipitate the secretory IgA

Methodology Applied
Scientific EffectPrecipitation: Precipitation

Implementation Method 2

a pasteurised intestinal secretory IgA-containing intestinal luminal fluid preparation

Methodology Applied
Scientific EffectPasteurization: Heating

Data Source

PatentEP2941300B1Secretory iga compositions, methods of making and methods of use thereof
Publication Date: 2020.12.09 WISCONSIN ALUMNI RES FOUND

AI summary

Described herein is secretory IgA isolated from the intestinal luminal fluid and intestinal mucosal of animals such as pigs and cows. Also included are methods of isolating secretory IgA. The secretory IgA is useful in food compositions such as animal and human food compositions as well as pharmaceutical compositions to increase growth rate, improve feed efficiency, reduce gastrointestinal inflammation, reduce a risk of gastrointestinal infection in the animal, or a combination thereof.