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分枝杆菌与天然免疫受体的相互作用:Toll样受体、C型凝集素和NOD样受体。

Mycobacterial interaction with innate receptors: TLRs, C-type lectins, and NLRs.

作者信息

Jo Eun-Kyeong

机构信息

Department of Microbiology, College of Medicine, Chungnam National University, Jungku, Daejeon, South Korea.

出版信息

Curr Opin Infect Dis. 2008 Jun;21(3):279-86. doi: 10.1097/QCO.0b013e3282f88b5d.

DOI:10.1097/QCO.0b013e3282f88b5d
PMID:18448973
Abstract

PURPOSE OF REVIEW

The recent discovery of novel classes of receptors, including toll-like receptors and nucleotide-binding oligomerization domain (NOD)-like receptors is challenging the crucial role of the innate immune system in the recognition of Mycobacterium tuberculosis. The present review is to focus on the roles and mechanisms of specific pattern-recognition receptor-microbial interaction for the host defense against mycobacterial infections.

RECENT FINDINGS

Toll-like receptors, key players in innate immunity, are now known to be important for the initiation and coordination of host responses to Mycobacterium tuberculosis. The interaction of Mycobacterium tuberculosis with toll-like receptors triggers intracellular signaling cascades that culminate in a proinflammatory response, but can also trigger signals that dampen the innate immune response. Other membrane-bound pattern-recognition receptors, including the mannose receptor, DC-SIGN, and Dectin-1, contribute to the propagation of Mycobacterium tuberculosis inflammatory signals, and Nod-like receptors (cytosolic pattern-recognition receptors) also act in modulating host recognition of Mycobacterium tuberculosis. Interactions between toll-like receptors and other pattern-recognition receptors are also evident in responses to Mycobacterium tuberculosis, as are possible mechanisms for coordination of innate and adaptive immunity.

SUMMARY

The complexity of Mycobacterium tuberculosis-pattern-recognition receptor interactions and their effects on host cell responses suggest key roles for innate immunity in controlling Mycobacterium tuberculosis, and the possibility of developing novel therapeutics for tuberculosis that target Mycobacterium tuberculosis-regulated innate immunity pathways.

摘要

综述目的

包括Toll样受体和核苷酸结合寡聚化结构域(NOD)样受体在内的新型受体的近期发现,正在挑战固有免疫系统在结核分枝杆菌识别中的关键作用。本综述旨在聚焦特定模式识别受体与微生物相互作用在宿主抵御分枝杆菌感染中的作用及机制。

最新发现

Toll样受体作为固有免疫的关键参与者,现已明确其对宿主针对结核分枝杆菌反应的启动和协调至关重要。结核分枝杆菌与Toll样受体的相互作用触发细胞内信号级联反应,最终导致促炎反应,但也可触发抑制固有免疫反应的信号。其他膜结合模式识别受体,包括甘露糖受体、DC-SIGN和Dectin-1,有助于结核分枝杆菌炎症信号的传播,Nod样受体(胞质模式识别受体)也参与调节宿主对结核分枝杆菌的识别。Toll样受体与其他模式识别受体之间的相互作用在对结核分枝杆菌的反应中也很明显,固有免疫和适应性免疫的协调机制也是如此。

总结

结核分枝杆菌与模式识别受体相互作用的复杂性及其对宿主细胞反应的影响表明,固有免疫在控制结核分枝杆菌方面发挥着关键作用,并且有可能开发出针对结核分枝杆菌调节的固有免疫途径的新型结核病治疗方法。

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