神经炎症
小胶质细胞
发病机制
炎症
免疫系统
神经科学
先天免疫系统
医学
多发性硬化
疾病
免疫学
阿尔茨海默病
生物
病理
作者
Frank L. Heppner,Richard M. Ransohoff,Burkhard Becher
摘要
The past two decades of research into the pathogenesis of Alzheimer disease (AD) have been driven largely by the amyloid hypothesis; the neuroinflammation that is associated with AD has been assumed to be merely a response to pathophysiological events. However, new data from preclinical and clinical studies have established that immune system-mediated actions in fact contribute to and drive AD pathogenesis. These insights have suggested both novel and well-defined potential therapeutic targets for AD, including microglia and several cytokines. In addition, as inflammation in AD primarily concerns the innate immune system - unlike in 'typical' neuroinflammatory diseases such as multiple sclerosis and encephalitides - the concept of neuroinflammation in AD may need refinement.
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