3.8 Article

High-density sub-100-nm peptide-gold nanoparticle complexes improve vaccine presentation by dendritic cells in vitro

Journal

NANOSCALE RESEARCH LETTERS
Volume 8, Issue -, Pages -

Publisher

SPRINGER
DOI: 10.1186/1556-276X-8-72

Keywords

Vaccines; Gold nanoparticles; ELISPOTs; Immunotherapy; Dendritic cells; Self-assembled monolayer

Funding

  1. Cell and Gene Therapy Center
  2. Cancer Prevention Research Institute of Texas (CPRIT)
  3. Department of Defense Congressionally Directed Medical Research Program [USAMRAA W81XWH-07-1-0428]
  4. Ruth L. Kirschstein National Research Service Awards [F30CA165686]
  5. Medical Scientist Training Program at Baylor College of Medicine

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Nanocarriers have been explored to improve the delivery of tumor antigens to dendritic cells (DCs). Gold nanoparticles are attractive nanocarriers because they are inert, non-toxic, and can be readily endocytosed by DCs. Here, we designed novel gold-based nanovaccines (AuNVs) using a simple self-assembling bottom-up conjugation method to generate high-peptide density delivery and effective immune responses with limited toxicity. AuNVs were synthesized using a self-assembling conjugation method and optimized using DC-to-splenocyte interferon-gamma enzyme-linked immunosorbent spot assays. The AuNV design has shown successful peptide conjugation with approximately 90% yield while remaining smaller than 80 nm in diameter. DCs uptake AuNVs with minimal toxicity and are able to process the vaccine peptides on the particles to stimulate cytotoxic T lymphocytes (CTLs). These high-peptide density AuNVs can stimulate CTLs better than free peptides and have great potential as carriers for various vaccine types.

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