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趋化因子系统的微生物破坏:一个不断扩展的范例。

Microbial corruption of the chemokine system: an expanding paradigm.

作者信息

Pease J E, Murphy P M

机构信息

Department of Applied Pharmacology, Imperial College School of Medicine at the National Heart and Lung Institute, Dovehouse Street, London, SW3 6LY, UK.

出版信息

Semin Immunol. 1998 Jun;10(3):169-78. doi: 10.1006/smim.1998.0129.

Abstract

The chemokine signaling system includes more than 40 secreted pro-inflammatory peptides and 12 G protein-coupled receptors that together orchestrate specific leukocyte trafficking in the mammalian immune system, ideally for anti- microbial defense and tissue repair processes. Paradoxically and perversely, some chemokines and chemokine receptors are also promicrobial factors and facilitate infectious disease, the result of either exploitation or subversion by specific microbes. Two modes of exploitation are known: usage of cellular chemokine receptors for cell entry by intracellular pathogens, including HIV, and usage of virally-encoded chemokine receptors for host cell proliferation. Likewise, two modes of subversion are known: virally-encoded chemokine antagonists and virally-encoded chemokine scavengers. Understanding how microbes turn the tables on the chemokine system may point to new methods to prevent or treat infection, or, more generally, to treat inappropriate chemokine-mediated inflammation.

摘要

趋化因子信号系统包括40多种分泌型促炎肽和12种G蛋白偶联受体,它们共同协调哺乳动物免疫系统中特定白细胞的运输,理想情况下用于抗菌防御和组织修复过程。矛盾的是,一些趋化因子和趋化因子受体也是促微生物因子,会促进传染病的发生,这是特定微生物利用或颠覆的结果。已知两种利用模式:细胞内病原体(包括HIV)利用细胞趋化因子受体进入细胞,以及病毒编码的趋化因子受体用于宿主细胞增殖。同样,已知两种颠覆模式:病毒编码的趋化因子拮抗剂和病毒编码的趋化因子清除剂。了解微生物如何扭转趋化因子系统的局面,可能会指向预防或治疗感染的新方法,或者更广泛地说,治疗不适当的趋化因子介导的炎症的新方法。

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