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Article
Biomimetic Antigenic Nanoparticles Elicit Controlled Protective Immune Response to Influenza
ACS Nano (2013)
  • Dustin Patterson, University of Texas at Tyler
Abstract
Here we present a biomimetic strategy toward nanoparticle design for controlled immune response through encapsulation of conserved internal influenza proteins on the interior of virus-like particles (VLPs) to direct CD8+ cytotoxic T cell protection. Programmed encapsulation and sequestration of the conserved nucleoprotein (NP) from influenza on the interior of a VLP, derived from the bacteriophage P22, results in a vaccine that provides multistrain protection against 100 times lethal doses of influenza in an NP specific CD8+ T cell-dependent manner. VLP assembly and encapsulation of the immunogenic NP cargo protein is the result of a genetically programmed self-assembly making this strategy amendable to the quick production of vaccines to rapidly emerging pathogens. Addition of adjuvants or targeting molecules were not required for eliciting the protective response.
Keywords
  • virus-like particle,
  • VLP,
  • P22,
  • nucleoprotein,
  • influenza,
  • CD8,
  • biomimetic
Disciplines
Publication Date
2013
DOI
10.1021/nn4006544
Publisher Statement
First published in ACS Nano.
Citation Information
Patterson, D. P., Rynda-Apple, A., Harmsen, A. L., Harmsen, A. G., & Douglas, T. (2013). Biomimetic Antigenic Nanoparticles Elicit Controlled Protective Immune Response to Influenza. ACS Nano, 7(4), 3036–3044.