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利用杂交膜囊泡的多抗原性抗菌纳米疫苗来对抗铜绿假单胞菌感染。

A multiantigenic antibacterial nanovaccine utilizing hybrid membrane vesicles for combating Pseudomonas aeruginosa infections.

机构信息

School of Pharmaceutical Sciences (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen, PR China.

Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.

出版信息

J Extracell Vesicles. 2024 Oct;13(10):e12524. doi: 10.1002/jev2.12524.

DOI:10.1002/jev2.12524
PMID:39400457
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11472236/
Abstract

Bacterial infections, especially those caused by multidrug-resistant pathogens, pose a significant threat to public health. Vaccines are a crucial tool in fighting these infections; however, no clinically available vaccine exists for the most common bacterial infections, such as those caused by Pseudomonas aeruginosa. Herein, a multiantigenic antibacterial nanovaccine (AuNP@HMV@SPs) is reported to combat P. aeruginosa infections. This nanovaccine utilizes the hybrid membrane vesicles (HMVs) created by fusing macrophage membrane vesicles (MMVs) with bacterial outer membrane vesicles (OMVs). The HMVs mitigate the toxic effects of both OMVs and bacterial secreted toxins (SP) adsorbed on the surface of MMVs, while preserving their stimulating properties. Gold nanoparticles (AuNPs) are utilized as adjuvant to enhance immune response without comprising safety. The nanovaccine AuNP@HMV@SPs induces robust humoral and cellular immune responses, leading to destruction of bacterial cells and neutralization of their secreted toxins. In murine models of septicemia and pneumonia caused by P. aeruginosa, AuNP@HMV@SPs exhibits superior prophylactic efficacy compared to control groups including OMVs, or MMVs@SPs and HMV@SPs, achieving 100% survival in septicemia and > 99.9% reduction in lung bacterial load in pneumonia. This study highlights AuNP@HMV@SPs as a safe and effective antibacterial nanovaccine, targeting both bacteria and their secreted toxins, and offers a promising platform for developing multiantigenic antibacterial vaccines against multidrug-resistant pathogens.

摘要

细菌感染,特别是由多药耐药病原体引起的感染,对公共卫生构成重大威胁。疫苗是对抗这些感染的重要工具;然而,目前还没有针对最常见细菌感染(如铜绿假单胞菌引起的感染)的临床可用疫苗。在此,报告了一种多抗原性抗菌纳米疫苗(AuNP@HMV@SPs),用于对抗铜绿假单胞菌感染。该纳米疫苗利用融合巨噬细胞膜囊泡(MMVs)与细菌外膜囊泡(OMVs)而成的混合膜囊泡(HMVs)。HMVs 减轻了 OMVs 和吸附在 MMVs 表面的细菌分泌毒素(SP)的毒性作用,同时保留了它们的刺激特性。金纳米粒子(AuNPs)被用作佐剂,以增强免疫反应而不影响安全性。纳米疫苗 AuNP@HMV@SPs 诱导强烈的体液和细胞免疫反应,导致细菌细胞的破坏和其分泌毒素的中和。在由铜绿假单胞菌引起的败血症和肺炎的小鼠模型中,与对照组(包括 OMVs 或 MMVs@SPs 和 HMV@SPs)相比,AuNP@HMV@SPs 表现出优越的预防功效,败血症中的存活率达到 100%,肺炎中的肺部细菌负荷减少>99.9%。本研究强调了 AuNP@HMV@SPs 作为一种安全有效的抗菌纳米疫苗,针对细菌及其分泌毒素,为开发针对多药耐药病原体的多抗原性抗菌疫苗提供了有前途的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/61c8c4c3eaee/JEV2-13-e12524-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/d35759077cc1/JEV2-13-e12524-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/fb247f56d593/JEV2-13-e12524-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/fec3258c7a38/JEV2-13-e12524-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/1630f3052ebc/JEV2-13-e12524-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/e734300dde6f/JEV2-13-e12524-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/61c8c4c3eaee/JEV2-13-e12524-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/d35759077cc1/JEV2-13-e12524-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/5742c648b360/JEV2-13-e12524-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/fb247f56d593/JEV2-13-e12524-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/fec3258c7a38/JEV2-13-e12524-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/1630f3052ebc/JEV2-13-e12524-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/e734300dde6f/JEV2-13-e12524-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f6/11472236/61c8c4c3eaee/JEV2-13-e12524-g003.jpg

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