4.8 Article

Aluminum oxide nanowires as safe and effective adjuvants for next-generation vaccines

Journal

MATERIALS TODAY
Volume 22, Issue -, Pages 58-66

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.mattod.2018.10.034

Keywords

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Funding

  1. Sila Nanotechnologies, Inc.
  2. Ministry of Healthcare of Ukraine
  3. Centre National de la Recherche Scientifique (CNRS)
  4. University of Lille
  5. Hauts-de-France region
  6. CPER Photonics for Society
  7. Volkswagen-Stiftung [90361]
  8. European Union [690836]
  9. Marie Curie Actions (MSCA) [690836] Funding Source: Marie Curie Actions (MSCA)

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Improving efficiency of an adjuvant, material that enhances the body's immune response to an antigen, has become vital for the development of safer, cheaper, and more effective next-generation vaccines. Commercial vaccines typically use aluminum salt-based adjuvant particles, most commonly aluminum oxyhydroxide (AlOOH) and aluminum hydroxide (Al(OH)(3)) based, often referred to as alum. Despite their broad use, their adjuvant properties are rather moderate. This is even worse in the case of aluminum oxide (Al2O3)-based adjuvant. While being more robust and less cytotoxic, Al2O3 is a significantly less effective adjuvant than above-mentioned Al compounds and is consequently not commonly used. Here, we report on the remarkably enhanced adjuvant properties of Al2O3 when produced in the form of nanowires (NWs). Based on recent advances in understanding neutrophil activation by inert nanoscaffolds, we have created ultra-long Al2O3 NWs with a high aspect ratio of similar to 1000. These NWs showed strong humoral immune response with no damaging effect on the microvasculature. Since only the change of shape of Al adjuvants is responsible for the excellent adjuvant properties, our finding holds great promise for rapid implementation as safer and more effective adjuvant alternative for human vaccines. The mechanism behind human blood-derived neutrophil activation with Al2O3 NWs was found to be sequestering of Al2O3 NWs by neutrophils via formation of neutrophil extracellular traps (NETs).

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