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

机译:高密度低于100 nm的肽-金纳米颗粒复合物可改善树突状细胞在体外的疫苗接种效果

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摘要

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.
机译:已经研究了纳米载体以改善肿瘤抗原向树突细胞(DC)的递送。金纳米颗粒是有吸引力的纳米载体,因为它们是惰性的,无毒的,并且易于被DC吞噬。在这里,我们设计了一种新颖的基于金的纳米疫苗(AuNV),它使用一种简单的自组装自下而上的缀合方法来产生高肽密度递送和有限毒性的有效免疫反应。使用自组装缀合方法合成AuNV,并使用DC到脾细胞干扰素γ酶联免疫吸附点测定法进行优化。 AuNV设计显示出成功的肽结合,产率约为90%,而直径仍小于80 nm。 DC以最小的毒性吸收AuNV,并且能够加工颗粒上的疫苗肽以刺激细胞毒性T淋巴细胞(CTL)。这些高肽密度的AuNV可以比游离肽更好地刺激CTL,并且具有作为各种疫苗类型的载体的巨大潜力。

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