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绕过补体:进化的启示与未来的影响。

Bypassing complement: evolutionary lessons and future implications.

作者信息

Atkinson John P, Frank Michael M

机构信息

Department of Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Clin Invest. 2006 May;116(5):1215-8. doi: 10.1172/JCI28622.

Abstract

Lectins like mannan-binding protein are part of the innate immune system. They circulate in association with serine proteases. Upon binding oligosaccharides, they activate the complement cascade analogous to the more familiar but evolutionarily more recent classical pathway, which is triggered by antibody binding to antigen. In this issue of the JCI, Selander et al. developed a sensitive and specific ELISA employing Salmonella-specific sugars to assess the activity of the lectin pathway of complement activation (see the related article beginning on page 1425). This more physiologic assay system allowed the investigators to rigorously define the requirements for lectin pathway activation. Furthermore, they uncovered an unsuspected means for this pathway to reach the desired critical step of activation of the opsonin C3. These types of functional assays will eventually replace the more laborious, less physiologic, and less informative approaches currently in use to monitor complement activation.

摘要

像甘露聚糖结合蛋白这样的凝集素是先天免疫系统的一部分。它们与丝氨酸蛋白酶结合循环。在结合寡糖后,它们激活补体级联反应,类似于更为人熟知但在进化上较新的经典途径,经典途径是由抗体与抗原结合触发的。在本期《临床研究杂志》中,塞兰德等人开发了一种灵敏且特异的酶联免疫吸附测定法,利用沙门氏菌特异性糖类来评估补体激活凝集素途径的活性(见第1425页开始的相关文章)。这种更符合生理的检测系统使研究人员能够严格界定凝集素途径激活的条件。此外,他们发现了该途径达到调理素C3激活这一关键步骤的一种意想不到的方式。这些类型的功能测定最终将取代目前用于监测补体激活的更为繁琐、不太符合生理且信息量较少的方法。

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