Modulating Antibacterial Immunity via Bacterial Membrane-Coated Nanoparticles

被引:479
作者
Gao, Weiwei
Fang, Ronnie H.
Thamphiwatana, Soracha
Luk, Brian T.
Li, Jieming
Angsantikul, Pavimol
Zhang, Qiangzhe
Hu, Che-Ming J.
Zhang, Liangfang [1 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Nanomedicine; biomimetic nanoparticle; membrane coating; infectious disease; bacterial vaccine; ERYTHROCYTE-MEMBRANE; BIOMIMETIC DELIVERY; SYNTHETIC VACCINES; VESICLES; FUNCTIONALIZATION; FUTURE; MICRO;
D O I
10.1021/nl504798g
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Synthetic nanoparticles coated with cellular membranes have been increasingly explored to harness natural cell functions toward the development of novel therapeutic strategies. Herein, we report on a unique bacterial membrane-coated nanoparticle system as a new and exciting antibacterial vaccine. Using Escherichia coli as a model pathogen, we collect bacterial outer membrane vesicles (OMVs) and successfully coat them onto small gold nanoparticles (AuNPs) with a diameter of 30 nm. The resulting bacterial membrane-coated AuNPs (BM-AuNPs) show markedly enhanced stability in biological buffer solutions. When injected subcutaneously, the BM-AuNPs induce rapid activation and maturation of dendritic cells in the lymph nodes of the vaccinated mice. In addition, vaccination with BM-AuNPs generates antibody responses that are durable and of higher avidity than those elicited by OMVs only. The BM-AuNPs also induce an elevated production of interferon gamma (INF gamma) and interleukin-17 (IL-17), but not interleukin-4 (IL-4), indicating its capability of generating strong Th1 and Th17 biased cell responses against the source bacteria. These observed results demonstrate that using natural bacterial membranes to coat synthetic nanoparticles holds great promise for designing effective antibacterial vaccines.
引用
收藏
页码:1403 / 1409
页数:7
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