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干扰素诱导的GTP酶与对细胞内病原体的免疫

IFN-inducible GTPases and immunity to intracellular pathogens.

作者信息

MacMicking John D

机构信息

Section of Microbial Pathogenesis, Boyer Center for Molecular Medicine, Yale University School of Medicine, 295 Congress Avenue, New Haven, CT 06536, USA.

出版信息

Trends Immunol. 2004 Nov;25(11):601-9. doi: 10.1016/j.it.2004.08.010.

Abstract

By eliciting host antimicrobial programs in nearly all nucleated cells interferons (IFNs) help orchestrate the innate immune response of mammals to a diverse array of microbial pathogens. Recent work has highlighted the complexity of this transcriptional repertoire and the emergence of several families of IFN-inducible guanosine 5' triphosphatases (GTPases)--p47, guanylate-binding protein (GBP), Mx and very large inducible GTPases (VLIG)--that subsume pathogen-specific roles. Such specificity arises from a combination of both the type and timing of inductive stimuli, target-cell population, subcellular binding partners and the infectious agent encountered. Evolution of different GTPase families to combat compartmentalized versus cytosolic pathogens reveals a hitherto unexpected level of intracellular discrimination during vertebrate host defense.

摘要

通过在几乎所有有核细胞中引发宿主抗菌程序,干扰素(IFN)有助于协调哺乳动物对多种微生物病原体的先天免疫反应。最近的研究突出了这种转录谱的复杂性,以及几个干扰素诱导型鸟苷5'三磷酸酶(GTP酶)家族的出现——p47、鸟苷酸结合蛋白(GBP)、Mx和非常大的诱导型GTP酶(VLIG)——它们具有病原体特异性作用。这种特异性源于诱导刺激的类型和时间、靶细胞群体、亚细胞结合伙伴以及所遇到的感染因子的综合作用。不同GTP酶家族为对抗分隔型与胞质病原体而发生的进化,揭示了脊椎动物宿主防御过程中迄今未被发现的细胞内区分水平。

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