4.7 Review

Functionalizing Ferritin Nanoparticles for Vaccine Development

Journal

PHARMACEUTICS
Volume 13, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics13101621

Keywords

ferritin nanoparticles; surface decoration; genetic fusion; modular assembly; vaccines; recombinant expression

Funding

  1. European Commission [602640, 730964, 823780]
  2. Portuguese Fundacao para a Ciencia e a Tecnologia (FCT) [IF/01704/2014, EXPL/BBB-BIO/1541/2013, DFA/BD/8167/2020]
  3. FCT/Ministerio da Ciencia, Tecnologia e Ensino Superior [UIDB/04462/2020, UIDP/04462/2020]
  4. Fundação para a Ciência e a Tecnologia [EXPL/BBB-BIO/1541/2013] Funding Source: FCT
  5. Marie Curie Actions (MSCA) [823780] Funding Source: Marie Curie Actions (MSCA)

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In the last decade, interest in ferritin-based vaccines has been growing due to their safety and immunogenicity. Phase I clinical trials for candidates targeting various pathogens are currently underway. However, challenges related to manufacturing and standardizing production processes need to be addressed to make ferritin-based therapeutics more widely available.
In the last decade, the interest in ferritin-based vaccines has been increasing due to their safety and immunogenicity. Candidates against a wide range of pathogens are now on Phase I clinical trials namely for influenza, Epstein-Barr, and SARS-CoV-2 viruses. Manufacturing challenges related to particle heterogeneity, improper folding of fused antigens, and antigen interference with intersubunit interactions still need to be overcome. In addition, protocols need to be standardized so that the production bioprocess becomes reproducible, allowing ferritin-based therapeutics to become readily available. In this review, the building blocks that enable the formulation of ferritin-based vaccines at an experimental stage, including design, production, and purification are presented. Novel bioengineering strategies of functionalizing ferritin nanoparticles based on modular assembly, allowing the challenges associated with genetic fusion to be circumvented, are discussed. Distinct up/down-stream approaches to produce ferritin-based vaccines and their impact on production yield and vaccine efficacy are compared. Finally, ferritin nanoparticles currently used in vaccine development and clinical trials are summarized.

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