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免疫刺激 DNA 水凝胶增强纳米毒素对细菌感染的保护效力。

Immunostimulatory DNA Hydrogel Enhances Protective Efficacy of Nanotoxoids against Bacterial Infection.

机构信息

Department of NanoEngineering, Chemical Engineering Program, and Moores Cancer Center, University of California San Diego, La Jolla, CA, 92093, USA.

出版信息

Adv Mater. 2023 Aug;35(31):e2211717. doi: 10.1002/adma.202211717. Epub 2023 Jun 20.

Abstract

While vaccines have been highly successful in protecting against various infections, there are still many high-priority pathogens for which there are no clinically approved formulations. To overcome this challenge, researchers have explored the use of nanoparticulate strategies for more effective antigen delivery to the immune system. Along these lines, nanotoxoids are a promising biomimetic platform that leverages cell membrane coating technology to safely deliver otherwise toxic bacterial antigens in their native form for antivirulence vaccination. Here, in order to further boost their immunogenicity, nanotoxoids formulated against staphylococcal α-hemolysin are embedded into a DNA-based hydrogel with immunostimulatory CpG motifs. The resulting nanoparticle-hydrogel composite is injectable and improves the in vivo delivery of vaccine antigens while simultaneously stimulating nearby immune cells. This leads to elevated antibody production and stronger antigen-specific cellular immune responses. In murine models of pneumonia and skin infection caused by methicillin-resistant Staphylococcus aureus, mice vaccinated with the hybrid vaccine formulation are well-protected. This work highlights the benefits of combining nanoparticulate antigen delivery systems with immunostimulatory hydrogels into a single platform, and the approach can be readily generalized to a wide range of infectious diseases.

摘要

虽然疫苗在预防各种感染方面非常成功,但仍有许多高度优先的病原体没有经过临床批准的制剂。为了克服这一挑战,研究人员探索了使用纳米颗粒策略更有效地将抗原递送到免疫系统。在这方面,纳米类毒素是一种有前途的仿生平台,利用细胞膜涂层技术以其天然形式安全地递呈 otherwise toxic bacterial antigens,用于抗病毒疫苗接种。在这里,为了进一步提高它们的免疫原性,针对金黄色葡萄球菌 α-溶血素的纳米类毒素被嵌入具有免疫刺激性 CpG 基序的基于 DNA 的水凝胶中。由此产生的纳米颗粒-水凝胶复合材料可注射,并改善疫苗抗原的体内递送,同时刺激附近的免疫细胞。这导致抗体产生增加和更强的抗原特异性细胞免疫反应。在耐甲氧西林金黄色葡萄球菌引起的肺炎和皮肤感染的小鼠模型中,用混合疫苗制剂接种的小鼠得到了很好的保护。这项工作强调了将纳米颗粒抗原递送系统与免疫刺激性水凝胶结合到单个平台的优势,并且该方法可以很容易地推广到广泛的传染病。

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