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

被引:110
|
作者
Chen, Yijie [1 ,2 ,3 ,4 ]
Chen, Mengchun [1 ,2 ,3 ,4 ]
Zhang, Yue [1 ,2 ]
Lee, Joo Hee [1 ,2 ]
Escajadillo, Tamara [5 ,6 ]
Gong, Hua [1 ,2 ]
Fang, Ronnie H. [1 ,2 ]
Gao, Weiwei [1 ,2 ]
Nizet, Victor [5 ,6 ]
Zhang, Liangfang [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[3] Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou 325027, Zhejiang, Peoples R China
[4] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325027, Zhejiang, Peoples R China
[5] Univ Calif San Diego, Dept Pediat, La Jolla, CA 92093 USA
[6] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
antivirulence; bacterial infection; detoxification; hemolytic toxin; nanosponge; STAPHYLOCOCCUS-AUREUS INFECTION; CELL-MEMBRANE; ALPHA-TOXIN; LISTERIOLYSIN-O; STREPTOLYSIN-O; VIRULENCE; NANOPARTICLES; HEMOLYSIN; DELIVERY; ANTIVIRULENCE;
D O I
10.1002/adhm.201701366
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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, -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.
引用
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页数:10
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