Development of PNAG-based vaccines

Vaccines using PNAG antigens with specific glucosamine monomer units and acetylation patterns, conjugated to bacteriophage QP capsids, address the challenge of inducing strong anti-carbohydrate responses, effectively combating antimicrobial-resistant pathogens like S. aureus.

AU2024402378A1Pending Publication Date: 2026-07-23BOARD OF TRUSTEES OPERATING MICHIGAN STATE UNIV +4
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Patent Information

Application Number
AU2024402378
Authority / Receiving Office
AU · AU
Patent Type
Applications
Current Assignee / Owner
Priority Date
2023-12-21
Filing Date
2024-12-19
Publication Date
2026-07-23

AI Technical Summary

Technical Problem

There is a need for effective vaccines against antimicrobial-resistant pathogens like Staphylococcus aureus, as current strategies face challenges in inducing strong anti-carbohydrate antibody responses without triggering high anti-carrier antibody responses, and existing vaccines are ineffective against strains such as methicillin-resistant S. aureus (MRSA).

Method used

Development of vaccine compositions comprising poly-0-(1->6)-N-acetylglucosamine (PNAG) antigens, specifically designed with varying glucosamine monomer units and acetylation patterns, conjugated to carrier systems like bacteriophage QP capsids to enhance immune response and reduce anti-carrier antibody interference.

Benefits of technology

The PNAG-based vaccines elicit high levels of anti-PNAG IgG antibodies, providing effective protection against S. aureus infections, including MRSA, with prolonged antibody responses and improved opsonic killing activities.

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Abstract

Provided herein are vaccine composition comprising poly-β-(l-6)-7N-acetylglucosamine (PNAG) antigen conjugated to capsid protein carrier, wherein said capsid comprises wild type or native sequence, or at least one mutation, and wherein the PNAG antigen comprises at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 glucosamine monomers, wherein at least one glucosamine monomer is acetylated.
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