Chimeric Peptide Vaccine Design for Broad Immune Response

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Solution Overview

Problem

Current vaccine development methods are inadequate for viruses like HCV, CMV, and Influenza, which exhibit high mutation frequencies and persistence in the body, leading to chronic infections and evading immune surveillance, necessitating new approaches to stimulate effective adaptive immune responses.

Innovation Solution

Design of cell-penetrating peptides that can be taken up by antigen-presenting cells, processed, and presented to T-lymphocytes to stimulate both CD4+ and CD8+ T-lymphocyte responses, utilizing specific amino acid sequences that enhance uptake and immune response induction.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional inactivated virus vaccines are used, then antibody responses are induced, but cell-mediated immunity is not effectively stimulated

Engineering Contradiction:
Improveimmune response effectivenessVSAvoidimmune response type
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent combines epitope peptides from multiple viral sources (HCV, CMV, Influenza) into a single chimeric peptide construct that can simultaneously stimulate both humoral and cell-mediated immune responses through a single vaccination approach

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The cell-penetrating peptide sequence acts as an intermediary that facilitates the delivery of epitope peptides into antigen-presenting cells, enabling effective presentation to T-lymphocytes and stimulation of cell-mediated immunity

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If live attenuated vaccines are used, then both cell-mediated immunity and antibody response are induced, but the virus must be replication competent which raises safety concerns

Engineering Contradiction:
Improveimmune response completenessVSAvoidsafety risk
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent extracts only the essential immunogenic components (epitope peptides) from the complete virus structure, removing the replication-competent viral genome while retaining the ability to stimulate both humoral and cell-mediated immune responses

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The vaccine construct is segmented into distinct functional modules: cell-penetrating peptide sequences for delivery, epitope peptides from multiple viruses for broad immunity, and linkers for structural integrity, allowing independent optimization of each component

Inventive Principle:
Principle #1Segmentation

3Productivity

If peptides are designed to penetrate cell membranes, then uptake by antigen-presenting cells is enhanced, but peptide structure complexity increases

Engineering Contradiction:
Improvecell uptake efficiencyVSAvoidpeptide structure
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent utilizes specific amino acid sequence parameters (basic residues like arginine and lysine at defined positions) to confer cell-penetrating properties on the peptide construct, optimizing the balance between uptake efficiency and structural complexity

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 peptides effectively penetrate cells and induce a cytotoxic T-lymphocyte and humoral immune response, providing a novel mechanism for vaccine development against viruses with high mutation rates and persistence.

Implementation Method 1

Several peptides have been demonstrated to translocate across the plasma membrane of eukaryotic cells by a seemingly energy-independent pathway. These peptides are defined as cell-penetrating peptides (CPPs).

Methodology Applied
Scientific EffectCell-penetrating peptide translocation:

Data Source

PatentEP2646459B1Peptide scaffold design
Publication Date: 2020.01.08 BIONOR IMMUNO
  • EP2646459B1 patent drawing
  • EP2646459B1 patent drawing
  • EP2646459B1 patent drawing

AI summary

The present invention relates to novel peptides and methods for treatment, diagnosis and prognosis of virus infections including infections with HCV, HIV, CMV and Influenza. The invention further relates to methods for identifying and providing peptides useful for the treatment and diagnosis.