Serotype 9N Glycoconjugates With Controlled Saccharide Sizing

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Solution Overview

Problem

Streptococcus pneumoniae serotype 9N polysaccharides are difficult to handle due to their viscosity, and existing vaccines do not induce a robust immune response effectively.

Innovation Solution

Development of Streptococcus pneumoniae serotype 9N glycoconjugates through covalent or non-covalent bonding of capsular saccharides to carrier proteins, with optional spacers, using chemical or mechanical sizing to achieve optimal molecular weights and conjugation yields.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If polysaccharide chains are large and viscous (as in serotype 9N), then immune response potential is high, but handling difficulty increases

Engineering Contradiction:
Improveimmune response robustnessVSAvoidhandling ease
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent applies segmentation by dividing the large polysaccharide chains into smaller oligosaccharide units through controlled hydrolysis. This reduces viscosity and improves handling while preserving immunogenicity, as the oligosaccharides can still elicit robust immune responses when conjugated to carrier proteins.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent changes the molecular size parameter of the polysaccharide from large chains to smaller oligosaccharide units. This parameter change reduces viscosity and handling difficulty while maintaining the immunogenic properties needed for robust immune response through conjugation to carrier proteins.

Inventive Principle:
Principle #35Parameter changes

2Reliability

If polysaccharide chains are large and viscous, then immune response potential is high, but conjugation yield decreases

Engineering Contradiction:
Improveimmune response robustnessVSAvoidconjugation yield
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent segments large polysaccharide chains into smaller oligosaccharide units, which improves conjugation yield by making the molecules more accessible and reactive. The smaller units can be more efficiently conjugated to carrier proteins while still maintaining robust immune response capability.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent changes the molecular size parameter from large polysaccharide chains to smaller oligosaccharide units. This parameter optimization simultaneously improves conjugation yield and maintains immunogenicity, resolving the contradiction between productivity and reliability.

Inventive Principle:
Principle #35Parameter changes

3Ease of manufacture

If conventional vaccines are used, then production is simple, but immune response is not robust

Engineering Contradiction:
Improveproduction simplicityVSAvoidimmune response robustness
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent creates composite materials by conjugating oligosaccharide units to carrier proteins. This composite structure combines the immunogenic properties of the polysaccharide with the immunological adjuvant effects of the protein carrier, producing robust immune responses while maintaining relatively simple production processes.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The patent uses carrier proteins as intermediaries to enhance the immune response to oligosaccharide antigens. The carrier protein acts as a mediator that improves immunogenicity through conjugation, allowing robust immune responses to be achieved without significantly complicating the manufacturing process.

Inventive Principle:
Principle #24Intermediary (Mediator)

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 glycoconjugates generate a more robust immune response and are produced with improved efficiency and operational simplicity.

Implementation Method 1

covalent or non-covalent bonding of capsular saccharides to carrier proteins

Methodology Applied
Scientific EffectCovalent bonding: Chemical Bonding

Implementation Method 2

covalent or non-covalent bonding of capsular saccharides to carrier proteins

Methodology Applied
Scientific EffectNon-covalent bonding: Chemical Bonding

Implementation Method 3

chemical or mechanical sizing to achieve optimal molecular weights and conjugation yields

Methodology Applied
Scientific EffectChemical sizing: Hydrolysis

Implementation Method 4

chemical or mechanical sizing to achieve optimal molecular weights and conjugation yields

Methodology Applied
Scientific EffectMechanical sizing: Mechanical Force

Data Source

PatentUS20260014241A1Immunogenic compositions comprising conjugated capsular saccharide antigens and uses thereof
Publication Date: 2026.01.15 PFIZER INC
  • US20260014241A1 patent drawing
  • US20260014241A1 patent drawing
  • US20260014241A1 patent drawing

AI summary

The present invention relates to new conjugated capsular saccharide antigens (glycoconjugates), immunogenic compositions comprising said glycoconjugates and uses thereof.