Kings College London Institute of Psychiatry, De Crespigny Park, London, UK.
Immunobiology. 2012 Feb;217(2):204-15. doi: 10.1016/j.imbio.2011.07.023. Epub 2011 Jul 23.
There is increasing evidence from genetic, immunohistochemical, proteomic and epidemiological studies as well as in model systems that complement activation has an important role in the pathogenesis of Alzheimer's disease (AD). The complement cascade is an essential element of the innate immune response. In the brain complement proteins are integral components of amyloid plaques and complement activation occurs at the earliest stage of the disease. The complement cascade has been implicated as a protective mechanism in the clearance of amyloid, and in a causal role through chronic activation of the inflammatory response. In this review we discuss the potential for complement activation to act as a biomarker for AD at several stages in the disease process. An accurate biomarker that has sufficient predictive, diagnostic and prognostic value would provide a significant opportunity to develop and test for effective novel therapies in the treatment of AD.
越来越多的遗传、免疫组化、蛋白质组学和流行病学研究以及模型系统的证据表明,补体激活在阿尔茨海默病(AD)的发病机制中起着重要作用。补体级联反应是先天免疫反应的一个重要组成部分。在大脑中,补体蛋白是淀粉样斑块的组成部分,并且在疾病的最早阶段就会发生补体激活。补体级联反应被认为是清除淀粉样蛋白的保护机制,通过慢性激活炎症反应也发挥着因果作用。在这篇综述中,我们讨论了补体激活在疾病过程的几个阶段作为 AD 生物标志物的可能性。一个准确的生物标志物,如果具有足够的预测、诊断和预后价值,将为开发和测试 AD 治疗的有效新疗法提供一个重要的机会。