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原位捕获细菌毒素用于抗毒力疫苗接种。

In Situ Capture of Bacterial Toxins for Antivirulence Vaccination.

机构信息

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

Department of Pharmaceutics, School of Pharmacy, Fudan University, Key Laboratory of Smart Drug Delivery (Fudan University), Ministry of Education, Shanghai, 201203, P. R. China.

出版信息

Adv Mater. 2017 Sep;29(33). doi: 10.1002/adma.201701644. Epub 2017 Jun 28.

Abstract

Antivirulence vaccination is a promising strategy for addressing bacterial infection that focuses on removing the harmful toxins produced by bacteria. However, a major challenge for creating vaccines against biological toxins is that the vaccine potency is often limited by lack of antigenic breadth, as most formulations have focused on single antigens, while most bacteria secrete a plethora of toxins. Here, a facile approach for generating multiantigenic nanotoxoids for use as vaccines against pathogenic bacteria by leveraging the natural affinity of virulence factors for cellular membranes is reported. Specifically, multiple virulent toxins from bacterial protein secretions are concurrently and naturally entrapped using a membrane-coated nanosponge construct. The resulting multivalent nanotoxoids are capable of delivering virulence factors together, are safe both in vitro and in vivo, and can elicit functional immunity capable of combating live bacterial infections in a mouse model. Despite containing the same bacterial antigens, the reported nanotoxoid formulation consistently outperforms a denatured protein preparation in all of the metrics studied, which underscores the utility of biomimetic nanoparticle-based neutralization and delivery. Overall this strategy helps to address major hurdles in the design of antivirulence vaccines, enabling increased antigenic breadth while maintaining safety.

摘要

抗毒力疫苗接种是一种有前途的策略,可以解决细菌感染问题,其重点是消除细菌产生的有害毒素。然而,针对生物毒素创造疫苗的一个主要挑战是,由于大多数制剂都集中在单一抗原上,而大多数细菌会分泌大量毒素,因此疫苗效力往往受到抗原广度的限制。在这里,报道了一种通过利用毒力因子与细胞膜的天然亲和力,生成用于对抗致病性细菌的多抗原纳米类毒素作为疫苗的简便方法。具体而言,使用膜涂层纳米海绵构建体同时并自然捕获来自细菌蛋白质分泌的多种毒力毒素。由此产生的多价纳米类毒素能够共同传递毒力因子,在体外和体内均安全,并且能够引发功能性免疫,能够在小鼠模型中抵抗活细菌感染。尽管含有相同的细菌抗原,但与研究中所有指标相比,所报道的纳米类毒素制剂始终优于变性蛋白制剂,这突出了基于仿生纳米粒子的中和和递呈的实用性。总的来说,该策略有助于解决抗毒力疫苗设计中的主要障碍,在保持安全性的同时增加抗原广度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc53/5581250/b94787efd2e8/nihms896948f1.jpg

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