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微生物发病机制中的巨噬细胞:防御逃避机制的共性。

Macrophages in Microbial Pathogenesis: Commonalities of Defense Evasion Mechanisms.

机构信息

Department of Biochemistry, School of Chemical and Life Sciences, Jamia Hamdard University, New Delhi, India.

Department of Immunology and Microbiology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, Colorado, USA.

出版信息

Infect Immun. 2022 May 19;90(5):e0029121. doi: 10.1128/IAI.00291-21. Epub 2021 Nov 15.

DOI:10.1128/IAI.00291-21
PMID:34780281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9119111/
Abstract

Macrophages are key arsenals of the immune system against invaders. After compartmental isolation of a pathogen in phagosomes, the host immune response attempts to neutralize the pathogen. However, pathogens possess the ability to subvert these assaults and can also convert macrophages into their replicative niche. The multiple host defense evasion mechanisms employed by these pathogens include phagosome maturation arrest, molecular mimicry through secretory antigens, interference with host signaling, active radical neutralization, inhibition of phagosome acidification, alteration of programmed cell death, and other mechanisms. Macrophage biology as a part of the host-pathogen interaction has expanded rapidly in the past decade. The present review aims to shed some light upon the macrophage defense evasion strategies employed by pathogens. We have also incorporated recent knowledge in the field of macrophage dynamics during infection and evolutionary perspectives of macrophage dynamics.

摘要

巨噬细胞是免疫系统对抗病原体的主要武器。在吞噬体中将病原体隔离开后,宿主的免疫反应试图中和病原体。然而,病原体具有颠覆这些攻击的能力,并且还可以将巨噬细胞转化为其复制龛。这些病原体采用的多种宿主防御逃避机制包括吞噬体成熟阻滞、通过分泌抗原进行分子模拟、干扰宿主信号、主动自由基中和、抑制吞噬体酸化、改变程序性细胞死亡等。过去十年中,巨噬细胞生物学作为宿主-病原体相互作用的一部分迅速发展。本综述旨在阐明病原体逃避巨噬细胞防御的策略。我们还结合了感染期间巨噬细胞动力学领域的最新知识和巨噬细胞动力学的进化观点。

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本文引用的文献

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Nat Commun. 2020 Sep 11;11(1):4549. doi: 10.1038/s41467-020-18287-x.
2
The SrrAB two-component system regulates pathogenicity through redox sensitive cysteines.SrrAB 双组份系统通过氧化还原敏感半胱氨酸调节致病性。
Proc Natl Acad Sci U S A. 2020 May 19;117(20):10989-10999. doi: 10.1073/pnas.1921307117. Epub 2020 Apr 30.
3
Escaping the Phagocytic Oxidative Burst: The Role of SODB in the Survival of Within Macrophages.逃避吞噬性氧化爆发:超氧化物歧化酶B在巨噬细胞内生存中的作用
Front Microbiol. 2020 Mar 10;11:326. doi: 10.3389/fmicb.2020.00326. eCollection 2020.
4
Monocytes and the Host Response to Fungal Pathogens.单核细胞与宿主对真菌病原体的反应。
Front Cell Infect Microbiol. 2020 Feb 13;10:34. doi: 10.3389/fcimb.2020.00034. eCollection 2020.
5
Salmonella-Driven Polarization of Granuloma Macrophages Antagonizes TNF-Mediated Pathogen Restriction during Persistent Infection.沙门氏菌驱动的肉芽肿巨噬细胞极化拮抗 TNF 介导体在持续性感染期间的病原体限制。
Cell Host Microbe. 2020 Jan 8;27(1):54-67.e5. doi: 10.1016/j.chom.2019.11.011. Epub 2019 Dec 26.
6
IL-4/IL-13 polarization of macrophages enhances Ebola virus glycoprotein-dependent infection.白细胞介素 4/13 对巨噬细胞的极化增强了埃博拉病毒糖蛋白依赖性感染。
PLoS Negl Trop Dis. 2019 Dec 11;13(12):e0007819. doi: 10.1371/journal.pntd.0007819. eCollection 2019 Dec.
7
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Inflammatory monocytes are detrimental to the host immune response during acute infection with Cryptococcus neoformans.在新型隐球菌急性感染期间,炎性单核细胞对宿主免疫反应有害。
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9
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Trends Immunol. 2019 Feb;40(2):113-127. doi: 10.1016/j.it.2018.12.007. Epub 2019 Jan 6.
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Front Cell Infect Microbiol. 2018 Sep 18;8:327. doi: 10.3389/fcimb.2018.00327. eCollection 2018.