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人类致病细菌的补体逃避策略

Complement Evasion Strategies of Human Pathogenic Bacteria.

作者信息

Sharma Shikhar, Bhatnagar Rakesh, Gaur Deepak

机构信息

Laboratory of Malaria and Vaccine Research, School of Biotechnology, Jawaharlal Nehru University, New Mehrauli Road, New Delhi, 110067 India.

Molecular Biology and Genetic Engineering Laboratory, School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.

出版信息

Indian J Microbiol. 2020 Sep;60(3):283-296. doi: 10.1007/s12088-020-00872-9. Epub 2020 Apr 24.

DOI:10.1007/s12088-020-00872-9
PMID:32655196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7329968/
Abstract

Human pathogens need to overcome an elaborate network of host defense mechanisms in order to establish their infection, colonization, proliferation and eventual dissemination. The interaction of pathogens with different effector molecules of the immune system results in their neutralization and elimination from the host. The complement system is one such integral component of innate immunity that is critically involved in the early recognition and elimination of the pathogen. Hence, under this immune pressure, all virulent pathogens capable of inducing active infections have evolved immune evasive strategies that primarily target the complement system, which plays an essential and central role for host defense. Recent reports on several bacterial pathogens have elucidated the molecular mechanisms underlying complement evasion, inhibition of opsonic phagocytosis and cell lysis. This review aims to comprehensively summarize the recent findings on the various strategies adopted by pathogenic bacteria to escape complement-mediated clearance.

摘要

人类病原体需要克服宿主防御机制的复杂网络,才能建立感染、定植、增殖并最终传播。病原体与免疫系统不同效应分子的相互作用导致它们被中和并从宿主体内清除。补体系统是固有免疫的一个重要组成部分,在病原体的早期识别和清除中起关键作用。因此,在这种免疫压力下,所有能够引发活动性感染的致病性病原体都进化出了主要针对补体系统的免疫逃避策略,而补体系统在宿主防御中起着至关重要的核心作用。最近关于几种细菌病原体的报道阐明了补体逃避、抑制调理吞噬作用和细胞裂解的分子机制。本综述旨在全面总结致病细菌为逃避补体介导的清除而采用的各种策略的最新研究结果。

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本文引用的文献

1
Poly-γ-D-Glutamate Capsule Inhibits Opsonic Phagocytosis by Impeding Complement Activation.聚γ-谷氨酸胶囊通过阻碍补体激活来抑制调理吞噬作用。
Front Immunol. 2020 Mar 31;11:462. doi: 10.3389/fimmu.2020.00462. eCollection 2020.
2
Elucidating the Immune Evasion Mechanisms of , the Causative Agent of Lyme Disease.阐明莱姆病病原体的免疫逃逸机制。
Front Immunol. 2019 Nov 26;10:2722. doi: 10.3389/fimmu.2019.02722. eCollection 2019.
3
Compendium of current complement therapeutics.补体治疗学最新概览。
Mol Immunol. 2019 Oct;114:341-352. doi: 10.1016/j.molimm.2019.07.030. Epub 2019 Aug 22.
4
The interaction of two novel putative proteins of with E-cadherin, plasminogen and complement components with potential role in bacterial infection.与 E-钙黏蛋白、纤溶酶原和补体成分的相互作用,这两种新型假定蛋白可能在细菌感染中起作用。
Virulence. 2019 Dec;10(1):734-753. doi: 10.1080/21505594.2019.1650613.
5
The hijackers guide to escaping complement: Lessons learned from pathogens.劫持者逃避补体的指南:从病原体中吸取的教训。
Mol Immunol. 2019 Oct;114:49-61. doi: 10.1016/j.molimm.2019.07.018. Epub 2019 Jul 20.
6
Clinical promise of next-generation complement therapeutics.下一代补体治疗药物的临床前景。
Nat Rev Drug Discov. 2019 Sep;18(9):707-729. doi: 10.1038/s41573-019-0031-6. Epub 2019 Jul 19.
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Kingella kingae Surface Polysaccharides Promote Resistance to Neutrophil Phagocytosis and Killing.金氏金菌表面多糖促进抵抗中性粒细胞吞噬和杀伤。
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