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细菌衍生的细胞外囊泡:内源性作用、治疗潜力及其仿生学在脓毒症治疗和预防中的应用。

Bacteria-derived extracellular vesicles: endogenous roles, therapeutic potentials and their biomimetics for the treatment and prevention of sepsis.

机构信息

Department of Critical Care Medicine, The First Affiliated Hospital of Zhengzhou University, Henan Engineering Research Center for Critical Care Medicine, Henan Key Laboratory of Critical Care Medicine, Zhengzhou, China.

Department of Emergency Medicine, The First Affiliated Hospital of Zhengzhou University, Henan Engineering Research Center for Critical Care Medicine, Henan Key Laboratory of Critical Care Medicine, Zhengzhou, China.

出版信息

Front Immunol. 2024 Feb 13;15:1296061. doi: 10.3389/fimmu.2024.1296061. eCollection 2024.


DOI:10.3389/fimmu.2024.1296061
PMID:38420121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10899385/
Abstract

Sepsis is one of the medical conditions with a high mortality rate and lacks specific treatment despite several years of extensive research. Bacterial extracellular vesicles (bEVs) are emerging as a focal target in the pathophysiology and treatment of sepsis. Extracellular vesicles (EVs) derived from pathogenic microorganisms carry pathogenic factors such as carbohydrates, proteins, lipids, nucleic acids, and virulence factors and are regarded as "long-range weapons" to trigger an inflammatory response. In particular, the small size of bEVs can cross the blood-brain and placental barriers that are difficult for pathogens to cross, deliver pathogenic agents to host cells, activate the host immune system, and possibly accelerate the bacterial infection process and subsequent sepsis. Over the years, research into host-derived EVs has increased, leading to breakthroughs in cancer and sepsis treatments. However, related approaches to the role and use of bacterial-derived EVs are still rare in the treatment of sepsis. Herein, this review looked at the dual nature of bEVs in sepsis by highlighting their inherent functions and emphasizing their therapeutic characteristics and potential. Various biomimetics of bEVs for the treatment and prevention of sepsis have also been reviewed. Finally, the latest progress and various obstacles in the clinical application of bEVs have been highlighted.

摘要

脓毒症是一种死亡率较高的医疗状况,尽管经过多年的广泛研究,仍然缺乏特异性治疗方法。细菌细胞外囊泡(bEVs)作为脓毒症病理生理学和治疗的一个新靶点而备受关注。源自致病微生物的细胞外囊泡(EVs)携带碳水化合物、蛋白质、脂质、核酸和毒力因子等致病因子,被视为引发炎症反应的“远程武器”。特别是 bEVs 的小尺寸可以穿过血脑和胎盘屏障,这些屏障是病原体难以穿透的,将病原体递送到宿主细胞,激活宿主免疫系统,并可能加速细菌感染过程和随后的脓毒症。多年来,对宿主来源的 EVs 的研究不断增加,为癌症和脓毒症的治疗带来了突破。然而,关于细菌衍生的 EVs 的作用和用途的相关方法在脓毒症治疗中仍然很少见。在此,通过强调其内在功能并强调其治疗特性和潜力,本文综述了 bEVs 在脓毒症中的双重性质。还综述了用于治疗和预防脓毒症的各种 bEVs 仿生学。最后,强调了 bEVs 在临床应用中的最新进展和各种障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/422bc9efab79/fimmu-15-1296061-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/27c00a722868/fimmu-15-1296061-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/a79eb81d567e/fimmu-15-1296061-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/933ada83aabf/fimmu-15-1296061-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/933167f779b0/fimmu-15-1296061-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/effabfea3d21/fimmu-15-1296061-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/422bc9efab79/fimmu-15-1296061-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/27c00a722868/fimmu-15-1296061-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/a79eb81d567e/fimmu-15-1296061-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/933ada83aabf/fimmu-15-1296061-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/933167f779b0/fimmu-15-1296061-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/effabfea3d21/fimmu-15-1296061-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54a8/10899385/422bc9efab79/fimmu-15-1296061-g006.jpg

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引用本文的文献

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Curr Microbiol. 2025-9-1

[2]
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[3]
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Precis Chem. 2025-3-28

[4]
Antibiotic treatment modulates -derived bacterial extracellular vesicle (BEV) production and their capacity to upregulate ICAM-1 in human endothelial cells.

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[5]
A proposed workflow to robustly analyze bacterial transcripts in RNAseq data from extracellular vesicles.

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[6]
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[7]
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[8]
RNA-containing extracellular vesicles in infection.

RNA Biol. 2024-1

[9]
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Cells. 2024-8-8

[10]
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Nano Converg. 2024-7-11

本文引用的文献

[1]
Cloaking Mesoporous Polydopamine with Bacterial Membrane Vesicles to Amplify Local and Systemic Antitumor Immunity.

ACS Nano. 2023-4-25

[2]
The role of platelets in immune-mediated inflammatory diseases.

Nat Rev Immunol. 2023-8

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Rethinking sepsis after a two-year battle with COVID-19.

Cell Mol Immunol. 2022-11

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Deep Learning-Enabled Raman Spectroscopic Identification of Pathogen-Derived Extracellular Vesicles and the Biogenesis Process.

Anal Chem. 2022-9-13

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The roles of extracellular vesicles in the immune system.

Nat Rev Immunol. 2023-4

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Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2022-9

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Trends Biotechnol. 2022-10

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Outer membrane vesicles produced by pathogenic strains of block autophagic flux and exacerbate inflammasome activation.

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