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Protein direct delivery to dendritic cells using nanoparticles based on amphiphilic poly(amino acid) derivatives.

机译:使用基于两亲性聚(氨基酸)衍生物的纳米粒子将蛋白质直接递送至树突状细胞。

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摘要

Induction of an adaptive immune response by vaccination is possible for a broad range of infectious diseases or cancers. Antigen-loaded polymeric nanoparticles have recently been shown to possess significant potential as vaccine delivery systems and adjuvants. Here we demonstrate the use of nanoparticles composed of amphiphilic poly(amino acid) derivatives as vaccine adjuvants. We prepared protein-loaded, biodegradable nanoparticles composed of hydrophobically modified poly(gamma-glutamic acid) (gamma-PGA). gamma-PGA hydrophobic derivatives (gamma-hPGA) formed 200 nm-sized nanoparticles in water. The protein-encapsulated gamma-hPGA nanoparticles were efficiently taken up by immature dendritic cells (iDCs). Interestingly, the nanoparticle uptake by iDCs induced DC maturation. The immunization with human immunodeficiency virus (HIV)-1 gp120-encapsulated nanoparticles strongly induced antigen-specific cellular immunity. These results suggest that antigen-loaded gamma-hPGA nanoparticles provide a novel delivery tool for vaccination against viral infections or tumors. This system has potential application as a universal delivery system for protein-based vaccines capable of inducing cytotoxic T lymphocyte (CTL).
机译:通过疫苗接种诱导适应性免疫应答对于多种传染病或癌症是可能的。最近已显示,载有抗原的聚合物纳米颗粒具有巨大的潜力,可以作为疫苗输送系统和佐剂。在这里,我们证明了由两亲性聚(氨基酸)衍生物组成的纳米颗粒作为疫苗佐剂的用途。我们准备了由疏水改性的聚(γ-谷氨酸)(γ-PGA)组成的蛋白质负载的,可生物降解的纳米颗粒。 γ-PGA疏水性衍生物(gamma-hPGA)在水中形成了200 nm大小的纳米颗粒。未成熟的树突状细胞(iDC)有效吸收了蛋白质包封的γ-hPGA纳米颗粒。有趣的是,iDC吸收纳米颗粒会诱导DC成熟。用人类免疫缺陷病毒(HIV)-1 gp120封装的纳米颗粒进行的免疫强烈诱导了抗原特异性细胞免疫。这些结果表明,载有抗原的γ-hPGA纳米颗粒为疫苗接种提供了一种新型工具,可用于抵抗病毒感染或肿瘤。该系统具有潜在用途,可作为能够诱导细胞毒性T淋巴细胞(CTL)的基于蛋白质的疫苗的通用递送系统。

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