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Acetalated dextran microparticles are a potent delivery platform for vaccine adjuvants in vitro

机译:乙酰化葡聚糖微粒是体外疫苗佐剂的有效递送平台

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In an effort to produce a more potent protein based vaccine, TLR 7 agonist imiquimod was encapsulated in microparticles made of the novel biomaterial, acetalated dextran (Ac-DEX). Ac-DEX is a pH sensitive biopolymer that degrades via the pH change present during antigen presenting cell (APC) phagocytosis. In vitro cytokine production and RT-PCR concludes that several inflammatory cytokines are upregulated in APCs cultured with imiquimod loaded Ac-DEX particles (MH-S and RAW 264.7 macrophages and bone marrow derived dendritic cells (BMDCs)). Dose sparing is observed, in that significantly less imiquimod is required for equivalent cell activation, compared to free imiquimod. Dose sparing, coupled with the passive targeting of APCs afforded with nanoparticle encapsulation, indicate that Ac-DEX encapsulated of imiquimod could increase protein vaccine efficacy.
机译:为了生产更有效的基于蛋白质的疫苗,将TLR 7激动剂咪喹莫特包裹在由新型生物材料缩醛化葡聚糖(Ac-DEX)制成的微粒中。 Ac-DEX是一种对pH敏感的生物聚合物,可通过抗原呈递细胞(APC)吞噬作用期间出现的pH变化而降解。体外细胞因子的产生和RT-PCR得出结论,在装有咪喹莫特的Ac-DEX颗粒(MH-S和RAW 264.7巨噬细胞和骨髓来源的树突状细胞(BMDC))培养的APC中,几种炎性细胞因子被上调。观察到剂量节省,因为与游离咪喹莫特相比,等效细胞活化所需的咪喹莫特明显更少。节省剂量,再加上用纳米颗粒封装提供的APC的被动靶向,表明用咪喹莫特封装的Ac-DEX可以提高蛋白质疫苗的功效。

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