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Aluminum hydroxide nanoparticles show a stronger vaccine adjuvant activity than traditional aluminum hydroxide microparticles

机译:氢氧化铝纳米粒子显示出比传统氢氧化铝微粒更强的疫苗佐剂活性

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摘要

Aluminum hydroxide is used as a vaccine adjuvant in various human vaccines. Unfortunately, despite its favorable safety profile, aluminum hydroxide can only weakly or moderately potentiate antigen-specific antibody responses. When dispersed in an aqueous solution, aluminum hydroxide forms particulates of 1-20 μm. There is increasing evidence that nanoparticles around or less than 200 nm as vaccine or antigen carriers have a more potent adjuvant activity than largemicroparticles. In the present study,we synthesized aluminumhydroxide nanoparticles of 112 nm. Using ovalbumin and Bacillus anthracis protective antigen protein as model antigens, we showed that protein antigens adsorbed on the aluminum hydroxide nanoparticles induced a stronger antigen-specific antibody response than the same protein antigens adsorbed on the traditional aluminum hydroxide microparticles of around 9.3 μm. The potent adjuvant activity of the aluminum hydroxide nanoparticles was likely related to their ability to more effectively facilitate the uptake of the antigens adsorbed on them by antigen-presenting cells. Finally, the local inflammation induced by aluminum hydroxide nanoparticles in the injection siteswasmilder than that induced by microparticles. Simply reducing the particle size of the traditional aluminum hydroxide adjuvant into nanometers represents a novel and effective approach to improve its adjuvanticity.
机译:氢氧化铝在各种人类疫苗中用作疫苗佐剂。不幸的是,尽管氢氧化铝具有良好的安全性,但它只能弱或中等地增强抗原特异性抗体反应。当分散在水溶液中时,氢氧化铝形成1-20μm的颗粒。越来越多的证据表明,作为疫苗或抗原载体的200 nm左右或小于200 nm的纳米颗粒比大颗粒具有更强的佐剂活性。在本研究中,我们合成了112 nm的氢氧化铝纳米颗粒。使用卵清蛋白和炭疽芽孢杆菌保护性抗原蛋白作为模型抗原,我们表明,与吸附在约9.3μm的传统氢氧化铝微粒上的相同蛋白抗原相比,吸附在氢氧化铝纳米颗粒上的蛋白抗原诱导了更强的抗原特异性抗体反应。氢氧化铝纳米颗粒的有效佐剂活性可能与它们更有效地促进抗原呈递细胞吸收吸附在其上的抗原的能力有关。最后,由氢氧化铝纳米颗粒在注射部位引起的局部炎症比由微粒引起的局部炎症弱。简单地将传统氢氧化铝佐剂的粒径减小至纳米代表一种改善其佐剂性的新颖有效的方法。

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