New Vaccine Design and Delivery Technologies
Open accessAbstract
Technological advances in immunology, protein design, and genetic delivery have unlocked new possibilities for vaccine concepts and delivery technologies that were previously inaccessible. These next-generation vaccine design efforts are particularly promising in their potential to provide solutions to challenging targets for which conventional approaches have proven ineffective-for example, a universal influenza vaccine. In this perspective, we discuss emerging approaches to vaccine design and engineering based on recent insights into immunology, structural biology, computational biology, and immunoengineering. We anticipate that these cutting-edge, interdisciplinary approaches will lead to breakthrough vaccine concepts for ever-evolving and (re)emerging influenza viruses, with important ramifications for global public health.
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Improved antigen delivery methods such as liposomes, polymeric particles, inorganic particles, outer membrane vesicles, immunostimulating complexes, and self-assembling protein nanoparticles have the potential to optimally enhance and skew immune responses to pathogens against which traditional vaccine approaches have been unsuccessful.
“These, and other methods such as self-assembling protein nanoparticles, have the potential to optimally enhance and skew the immune response to pathogens against which traditional vaccine approaches have proven to be unsuccessful129,134.”
From A guide to vaccinology: from basic principles to new developments (2021) · cites this paper as [134]
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A guide to vaccinology: from basic principles to new developments
Pollard, A. J., & Bijker, E. M. (2021) · Nature Reviews Immunology · doi:10.1038/s41577-020-00479-7 · Cited by 1,593 · see citing works
Walls, A. C., Fiala, B., Schäfer, A., Wrenn, S., Pham, M. N., Murphy, M., Tse, L. V., Shehata, L., O’Connor, M. A., Chen, C., et al. (2020) · Cell · doi:10.1016/j.cell.2020.10.043 · Cited by 532 · see citing works
Self-citation
- Authors
- Kanekiyo, M., Ellis, D., & King, N. P.
- Affiliations
- National Institutes of Health (US)
- University of Washington (US)
- Corresponding author
- Kanekiyo, Masaru
- Venue
- The Journal of Infectious Diseases
- Publisher
- Oxford University Press (OUP)
- Published
- 2019-04-08
- Volume
- 219
- Issue
- Supplement_1
- Pages
- S88-S96
- ISSN
- 0022-1899 (ISSN-L)
- 1537-6613
- PMC
- PMC6452296
- OpenAlex
- W2912432120
- Cited by
- 69
- References
- 51
- Citations by year
- 2026: 8 · 2025: 9 · 2024: 4 · 2023: 10 · 2022: 8 · 2021: 14 · 2020: 12 · 2019: 4
- FWCI
- 7.23
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Infectious Diseases (publishedVersion, public-domain)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases
- National Institutes of Health
- Open Philanthropy Project
- Topics
- Health Sciences › Medicine › Epidemiology › Influenza Virus Research Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Keywords
- vaccine design, universal influenza vaccine, influenza virus, immunoengineering, protein design, structural biology, computational biology
- MeSH terms
- Broadly Neutralizing Antibodies, Animals, Antibodies, Viral, Epitopes, Antigens, Viral, Disease Models, Animal, Humans, Influenza, Human, Influenza Vaccines, Orthomyxoviridae, Orthomyxoviridae Infections, RNA, Messenger, Vaccination, Protein Engineering, Antigen Presentation, Hemagglutinin Glycoproteins, Influenza Virus, Mice
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