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高密度亚 100nm 肽-金纳米颗粒复合物可提高树突状细胞体外递呈疫苗的效率。

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

机构信息

Department of Bioengineering, Rice University, 77005, Houston, TX USA.

出版信息

Nanoscale Res Lett. 2013 Feb 12;8(1):72. doi: 10.1186/1556-276X-8-72.


DOI:10.1186/1556-276X-8-72
PMID:23402570
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3579702/
Abstract

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-γ 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.

摘要

纳米载体已被探索用于提高肿瘤抗原递送至树突状细胞 (DC) 的效率。金纳米颗粒是一种很有吸引力的纳米载体,因为它们具有惰性、无毒且可以被 DC 轻易内吞。在这里,我们使用简单的自下而上的偶联方法设计了新型基于金的纳米疫苗 (AuNVs),以实现高肽密度的递呈和有效的免疫反应,同时毒性有限。AuNVs 是使用自组装偶联方法合成的,并使用 DC 向脾细胞 IFN-γ 酶联免疫斑点分析进行了优化。AuNV 设计成功地实现了约 90%的产率的肽偶联,同时直径仍保持在 80nm 以下。AuNVs 摄取 DC 具有最小的毒性,并且能够在颗粒上处理疫苗肽以刺激细胞毒性 T 淋巴细胞 (CTL)。这些高肽密度的 AuNVs 可以比游离肽更好地刺激 CTL,并且作为各种疫苗类型的载体具有巨大的潜力。

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

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本文引用的文献

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