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纳米类毒素疫苗

Nanotoxoid Vaccines.

作者信息

Hu Che-Ming J, Zhang Liangfang

机构信息

Department of NanoEngineering and Moores Cancer Center, University of California, San Diego, La Jolla, CA 92093, United States.

出版信息

Nano Today. 2014 Aug 1;9(4):401-404. doi: 10.1016/j.nantod.2014.06.001.

Abstract

To improve innate defense against diseases, vaccine formulations are routinely administered to mount immune responses against disease-causing organisms or their associated toxins. These formulations are typically prepared with weakened forms of microbes, their surface proteins, or their virulence factors, which can train the immune system to recognize and neutralize similar infectious threats in later exposures. Owing to many unique properties of nanoparticles in enhancing vaccine potency, nanoscale carriers are drawing increasing interest as a platform for developing safer and more effective vaccine formulations. Notably, a nanoparticle-based strategy was recently demonstrated to safely deliver intact, non-denatured protein toxins to mount a potent anti-toxin immune response. A biomimetic nanoparticle cloaked in biological membranes was used to sequester membrane-active toxins. Upon interaction with the nanoparticles, the toxins become retrained and lose their toxicity as they are precluded from interacting with cellular targets. The resulting particle/toxin complex adopts a nanoparticulate morphology that facilitates the toxins' intracellular delivery. This sequestration approach has immense immunological implications owing to its ability in enabling structurally preserved toxins for immune processing. This technique offers opportunities in novel toxoid vaccine designs that promise more effective anti-toxin immune responses and contrasts the existing paradigm in toxoid preparation, in which toxins are antigenically altered to ensure virulence removal. The potent nanotoxoid formulations provide a viable anti-virulence measure in combating microbial infections that involve membrane-damaging toxins, including methicillin-resistant (MRSA) and Group A streptococcal infections.

摘要

为了增强对疾病的先天防御能力,通常会接种疫苗制剂以引发针对致病生物体或其相关毒素的免疫反应。这些制剂通常由弱化形式的微生物、其表面蛋白或毒力因子制备而成,它们可以训练免疫系统在日后接触时识别并中和类似的感染威胁。由于纳米颗粒在增强疫苗效力方面具有许多独特特性,纳米级载体作为开发更安全、更有效疫苗制剂的平台正越来越受到关注。值得注意的是,最近证明了一种基于纳米颗粒的策略能够安全递送完整的、未变性的蛋白毒素,以引发有效的抗毒素免疫反应。一种包裹在生物膜中的仿生纳米颗粒被用于隔离膜活性毒素。与纳米颗粒相互作用后,毒素被截留,由于它们被阻止与细胞靶点相互作用而失去毒性。产生的颗粒/毒素复合物呈现纳米颗粒形态,便于毒素的细胞内递送。这种截留方法具有巨大的免疫学意义,因为它能够使结构保存的毒素进行免疫处理。这项技术为新型类毒素疫苗设计提供了机会,有望产生更有效的抗毒素免疫反应,与现有的类毒素制备范式形成对比,在现有的范式中,毒素经过抗原性改变以确保去除毒力。强效纳米类毒素制剂为对抗涉及膜损伤毒素的微生物感染提供了一种可行的抗毒力措施,包括耐甲氧西林金黄色葡萄球菌(MRSA)感染和A组链球菌感染。

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本文引用的文献

1
Nanoparticle-detained toxins for safe and effective vaccination.纳米颗粒滞留毒素用于安全有效的疫苗接种。
Nat Nanotechnol. 2013 Dec;8(12):933-8. doi: 10.1038/nnano.2013.254. Epub 2013 Dec 1.
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