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Microparticles as vaccine adjuvants and delivery systems
Abstract
Adjuvants can be broadly divided into two groups, based on their principal mechanisms of action: vaccine delivery systems and immunostimulatory adjuvants. Vaccine delivery systems are generally particulate (e.g., emulsions, microparticles, immunostimulatory complexes and liposomes) and function mainly to target associated antigens into antigen-presenting cells. However, increasingly, more complex formulations are being developed in which delivery systems are exploited both for the delivery of antigens and also for the delivery of coadministered immunostimulatory adjuvants. The rationale for this approach is to ensure that both antigen and adjuvant are delivered into the same population of antigen-presenting cells. In addition, delivery systems can focus the effect of the adjuvants onto the key cells of the immune system and limit the systemic distribution of the adjuvant, to minimize its potential to induce adverse effects. The formulation and delivery of potent adjuvants in microparticles may allow the development of prophylactic and therapeutic vaccines against cancers and chronic infectious diseases, which are currently poorly controlled. In addition, microparticle formulations may also allow vaccines to be delivered mucosally.
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“PLGA is not only a highly biocompatible and bio degradable material, it further affects the immune response via its adjuvant properties [50], which were hypothesized to be due to the particulate structure of the allergen carrier and due to the sustained allergen release from the particles [51].”
From Use of lectin-functionalized particles for oral immunotherapy (2012) · cites this paper as [50]
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Malyala, P., & Singh, M. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8412-6_19 · Cited by 2
Self-citationDelivery of Natural Products Using Polymeric Particles for Cancer Chemotherapeutics
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Infection Prevention: Oil- and Lipid-Containing Products in Vaccinology
Ebensen, T., Fuchs, B., Schulze, K., & Guzmán, C. A. (2020) · Springer eBooks · doi:10.1007/978-3-030-15147-8_25 · Cited by 1
Discovery of Vaccine Adjuvants
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Multi-compartmental delivery systems for peptide and DNA vaccines in melanoma immunotherapy
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Immunostimulatory Properties of Biodegradable Microparticles
Sharp, F. A., & Lavelle, E. C. (2012) · doi:10.1002/9781118345313.ch24
Patel, J. D. (2006) · UKnowledge (University of Kentucky)
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Metadata
- Authors
- O’Hagan, D. T., & Singh, M.
- ORCID
- Singh, Manmohan
- Venue
- Expert Review of Vaccines
- Publisher
- Informa UK Limited
- Published
- 2003-04
- Volume
- 2
- Issue
- 2
- Pages
- 269-283
- ISSN
- 1476-0584 (ISSN-L)
- 1744-8395
- OpenAlex
- W2030951969
- Cited by
- 214
- References
- 155
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 5 · 2023: 7 · 2022: 4 · 2021: 10 · 2020: 10 · 2019: 3 · 2018: 3 · 2017: 6 · 2016: 7 · 2015: 10 · 2014: 8 · 2013: 9 · 2012: 23
- FWCI
- 1.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Expert Review of Vaccines (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Keywords
- vaccine adjuvants, microparticles, vaccine delivery systems, immunostimulatory adjuvants, antigen-presenting cells, liposomes, emulsions, mucosal vaccine delivery, cancer vaccines
- MeSH terms
- Adjuvants, Immunologic, Animals, Antigens, Capsules, Humans, Immunity, Cellular, Lipid A, Microspheres, Oligodeoxyribonucleotides, Saponins, Vaccines, Cytokines, Drug Delivery Systems, Immunity, Mucosal, Vaccines, DNA
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