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外膜囊泡包被纳米颗粒疫苗可预防肺炎和败血症。

Outer Membrane Vesicle-Coated Nanoparticle Vaccine Protects Against Pneumonia and Sepsis.

作者信息

Bjanes Elisabet, Zhou Jiarong, Qayum Tariq, Krishnan Nishta, Zurich Raymond H, Menon Nitasha D, Hoffman Alexandria, Fang Ronnie H, Zhang Liangfang, Nizet Victor

机构信息

Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California 92093, USA.

Department of Nanoengineering, University of California San Diego, La Jolla, California 92093, USA.

出版信息

Adv Nanobiomed Res. 2023 Feb;3(2). doi: 10.1002/anbr.202200130. Epub 2022 Dec 22.

Abstract

The highly multidrug-resistant (MDR) Gram-negative bacterial pathogen is a top global health priority where an effective vaccine could protect susceptible populations and limit resistance acquisition. Outer membrane vesicles (OMVs) shed from Gram-negative bacteria are enriched with virulence factors and membrane lipids but heterogeneous in size and cargo. We report a vaccine platform combining precise and replicable nanoparticle technology with immunogenic OMVs (Ab-OMVs). Gold nanoparticle cores coated with Ab-OMVs (Ab-NPs) induced robust IgG titers in rabbits that enhanced human neutrophil opsonophagocytic killing and passively protected against lethal sepsis in mice. Active Ab-NP immunization in mice protected against sepsis and pneumonia, accompanied by B cell recruitment to draining lymph nodes, activation of dendritic cell markers, improved splenic neutrophil responses, and mitigation of proinflammatory cytokine storm. Nanoparticles are an efficient and efficacious platform for OMV vaccine delivery against and perhaps other high-priority MDR pathogens.

摘要

高度多重耐药(MDR)革兰氏阴性菌病原体是全球卫生领域的首要重点问题,有效的疫苗可保护易感人群并限制耐药性的产生。革兰氏阴性菌释放的外膜囊泡(OMV)富含毒力因子和膜脂,但大小和成分各异。我们报告了一种将精确且可复制的纳米颗粒技术与具有免疫原性的OMV(Ab-OMV)相结合的疫苗平台。包被有Ab-OMV的金纳米颗粒核心(Ab-NP)在兔体内诱导产生了强大的IgG滴度,增强了人类中性粒细胞的调理吞噬杀伤作用,并在小鼠中被动保护其免受致命性败血症的侵害。在小鼠中进行主动Ab-NP免疫可预防败血症和肺炎,同时伴有B细胞募集至引流淋巴结、树突状细胞标志物的激活、脾脏中性粒细胞反应的改善以及促炎细胞因子风暴的减轻。纳米颗粒是用于递送OMV疫苗以对抗[病原体名称缺失]以及可能的其他高优先级MDR病原体的高效且有效的平台。

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