Project Details
Description
The global emergence of antimicrobial resistance (AMR) is a growing concern that has sparked the search for alternative approaches to treat bacterial infections. Vaccination is widely considered to be the most effective single measure to protect populations against transmissible diseases without promoting AMR.
However, to date, there are very few vaccines against bacteria in general and in particular against AMR priority bacteria.The aim of this proposal is to design, produce, test, and protect multivalent nanoparticle vaccines against bacteria. The project is intended to prove three important concepts that could have significant implications for the development of new vaccines against AMR bacteria. The concepts are: 1) that the use of nanoparticles will elicit a significantly stronger immune response and a flexible way of designing multivalent vaccines, 2) that multivalent vaccines will significantly improve the level, persistence and range of protection and, in addition, counteract escape mutants and, 3) circulating antibody repertoire sequencing will generate molecular correlates of protection that can be used to understand the properties of a protective immune response.
The work holds the potential to demonstrate important generalizable concepts for vaccine development against bacteria and to generate new IP that can be used to explore the possibility of commercialization and conducting future human trials.
However, to date, there are very few vaccines against bacteria in general and in particular against AMR priority bacteria.The aim of this proposal is to design, produce, test, and protect multivalent nanoparticle vaccines against bacteria. The project is intended to prove three important concepts that could have significant implications for the development of new vaccines against AMR bacteria. The concepts are: 1) that the use of nanoparticles will elicit a significantly stronger immune response and a flexible way of designing multivalent vaccines, 2) that multivalent vaccines will significantly improve the level, persistence and range of protection and, in addition, counteract escape mutants and, 3) circulating antibody repertoire sequencing will generate molecular correlates of protection that can be used to understand the properties of a protective immune response.
The work holds the potential to demonstrate important generalizable concepts for vaccine development against bacteria and to generate new IP that can be used to explore the possibility of commercialization and conducting future human trials.
| Status | Active |
|---|---|
| Effective start/end date | 2022/12/01 → 2028/12/31 |
Funding
- Swedish Research Council

UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This project contributes towards the following SDG(s):
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SDG 3 Good Health and Well-being
Subject classification (UKÄ)
- Infectious Medicine
Research output
- 3 Article
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Antibody-guided identification of Achromobacter xylosoxidans protein antigens in cystic fibrosis.
Sahl, C., Chowdhury, S., Malmström, J. & Påhlman, L. I., 2025 May, In: mSphere. 10, 5, p. 1-14 e0023325.Research output: Contribution to journal › Article › peer-review
Open Access -
Dissecting the properties of circulating IgG against streptococcal pathogens through a combined systems antigenomics-serology workflow
Gomez Toledo, A., Chowdhury, S., Hjortswang, E., Sorrentino, J. T., Lewis, N. E., Bläckberg, A., Ekström, S., Kjellström, S., Izadi, A., Olofsson, B., Nordenfelt, P., Malmström, L., Rasmussen, M. & Malmström, J., 2025 Feb 24, In: Nature Communications. 16, p. 1-16 1942.Research output: Contribution to journal › Article › peer-review
Open Access -
Multimodal Mass Spectrometry Identifies a Conserved Protective Epitope in S. pyogenes Streptolysin O
Tang, D., Gueto-Tettay, C., Hjortswang, E., Ströbaek, J., Ekström, S., Happonen, L., Malmström, L. & Malmström, J., 2024 Jun 4, In: Analytical Chemistry. 96, 22, p. 9060–9068Research output: Contribution to journal › Article › peer-review
Open Access