AFM-LDH · Atomic force microscopy-based exploration of layered double hydroxide nanoparticles adjuvant mechanism
Horizon Europe — Marie Skłodowska-Curie Actions
- Duration
- 2023-09-01 → 2026-01-31
- EU contribution
- €230,774
- Participants
- 1
- Scheme
- HORIZON-TMA-MSCA-PF-EF
Lines connect the coordinator with its partners.
Results in brief
Atomic force microscopy-based exploration of layered double hydroxide nanoparticles adjuvant mechanism
For more than a century, aluminium-based adjuvants (collectively known as Alum) have been essential components of many licensed vaccines. Their long clinical history and safety profile have made them a cornerstone of modern immunisation programmes. However, traditional Alum adjuvants primarily stimulate antibody-mediated immunity and have limited capacity to induce robust CD8⁺ T-cell responses, which are crucial for protection against intracellular pathogens and for effective cancer immunotherapy. This limitation creates an important gap in current vaccine technology, particularly in a global health landscape increasingly shaped by emerging infectious diseases and the growing need for personalised cancer treatments. Recent advances in nanotechnology have led to the development of layered double hydroxide (LDH) nano-aluminium adjuvants (NA), engineered from clinically used aluminium hydroxide and magnesium hydroxide materials. These next-generation adjuvants show great promise: they can stimulate both strong antibody responses and potent CD8⁺ T-cell immunity. In addition to their role in vaccine formulations, NA materials can function as immunomodulators capable of reshaping the tumour microenvironment and enhancing CD8⁺ T-cell activity, offering potential therapeutic value in oncology. Despite these encouraging findings, the fundamental relationship between the chemical composition of NA and their immunological behaviour remains poorly understood. This knowledge gap limits the rational design and optimisation of NA-based vaccines and immunotherapies. This project aims to address this challenge by applying advanced physicochemical and biological characterisation techniques to systematically investigate how specific chemical features of NA influence their immunomodulatory mechanisms. By elucidating the chemistry-immunology relationship, the project seeks to establish a scientific basis for designing more effective and predictable nano-aluminium adjuvants. The expected outcomes will contribute to the development of next-generation vaccines and immunotherapies with broader efficacy, potentially benefiting public health at large and supporting strategic priorities in infectious disease preparedness and cancer treatment.
Data: CORDIS, © European Union
Project objective
Layered double hydroxides nanoparticles (LDH NPs) composed by divalent/trivalent metal ions are efficient vaccine adjuvants to assist antigens to induce potent humoral and cellular immunity. However, the adjuvant mechanisms of LDH NPs still remains elusive. Since the metal ion species and ratio are closely related to the adjuvant activity of LDH NPs, this study will investigate how the metal ion composition will affect the adjuvant activity of LDH NPs. Then, an atomic force microscopy (AFM)-based approach to physico-mechanically map the specific interaction occurring between NP and Toll-like receptor-4 or scavenger receptor A1 in vitro on living cells. Finally, the adjuvant signaling pathways of LDH NPs will be investigated in antigen presenting cells. This study will greatly advance the knowledge on the interplay among nanomaterials and innate immunity. The single-cell, quantitative approach can be readily applied to study the binding of other nanomaterials and the testing of anti-inflammatory molecules on living cells of the innate immune system.
Original text from CORDIS.
Participants
- AARHUS UNIVERSITET · Aarhus CCoordinatorDenmark
Links
- View on CORDIS
- DOI: 10.3030/101064861
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e50b314761&appId=PPGMS
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e52cde575f&appId=PPGMS
Data: CORDIS, © European Union
