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Erythrocyte membrane-coated nanogel for combinatorial antivirulence and responsive antimicrobial delivery against Staphylococcus aureus infection.红细胞膜包覆的纳米凝胶用于金黄色葡萄球菌感染的组合抗毒力和响应性抗菌药物递送。
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用红细胞膜包覆纳米海绵广谱中和形成孔的毒素。

Broad-Spectrum Neutralization of Pore-Forming Toxins with Human Erythrocyte Membrane-Coated Nanosponges.

机构信息

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

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China.

出版信息

Adv Healthc Mater. 2018 Jul;7(13):e1701366. doi: 10.1002/adhm.201701366. Epub 2018 Feb 13.

DOI:10.1002/adhm.201701366
PMID:29436150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6041168/
Abstract

Neutralization of bacterial toxins has become a compelling approach to treating bacterial infections as it may pose less selective pressure for the development of bacterial resistance. Currently, the majority of toxin neutralization platforms act by targeting the molecular structure of the toxin, which requires toxin identification and customized design for different diseases. Therefore, their development has been challenged by the enormous number and complexity of bacterial toxins. Herein, biomimetic toxin nanosponges are formulated by coating membranes of human red blood cells (hRBCs) onto polymeric nanoparticles, which act as a toxin decoy to absorb and neutralize a broad-spectrum of hemolytic toxins regardless of their molecular structure. When tested with model pore-forming toxins, including melittin, α-hemolysin of methicillin-resistant Staphylococcus aureus, listeriolysin O of Listeria monocytogenes, and streptolysin O of Group A Streptococcus, the hRBC nanosponges are able to completely inhibit toxin-induced hemolysis in a concentration-dependent manner. In addition, the nanosponge-detained toxins show no cytotoxicity when tested on human umbilical vein endothelial cells and no lethality when injected into mice, which together indicate effective toxin neutralization. Overall, these results demonstrate the broad applicability and high effectiveness of the hRBC nanosponges as a novel antivirulence platform against hemolytic toxins from various strains of bacteria.

摘要

细菌毒素的中和已成为治疗细菌感染的一种强制性方法,因为它可能对细菌耐药性的发展产生较小的选择性压力。目前,大多数毒素中和平台通过靶向毒素的分子结构起作用,这需要对不同疾病进行毒素鉴定和定制设计。因此,由于细菌毒素数量巨大且结构复杂,它们的开发受到了挑战。在此,通过将人红细胞(hRBC)的膜涂覆到聚合物纳米颗粒上,形成仿生毒素纳米海绵,这些纳米海绵作为毒素诱饵,能够吸收和中和广谱的溶血毒素,而不管其分子结构如何。当用模式孔形成毒素(包括蜂毒素、耐甲氧西林金黄色葡萄球菌的α-溶血素、李斯特菌溶血素 O 和 A 组链球菌的链球菌溶血素 O)进行测试时,hRBC 纳米海绵能够以浓度依赖的方式完全抑制毒素诱导的溶血。此外,在人脐静脉内皮细胞上测试时,被纳米海绵截留的毒素没有细胞毒性,在注射到小鼠中时也没有致死性,这共同表明了有效的毒素中和作用。总体而言,这些结果表明 hRBC 纳米海绵作为一种新型抗溶血毒素的抗病毒平台,可广泛应用于来自不同菌株的细菌的溶血毒素。