3.8 Article

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

期刊

NANOSCALE RESEARCH LETTERS
卷 8, 期 -, 页码 -

出版社

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

关键词

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

资金

  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

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据