Brothers Holly M, Wilcock Donna M
University of Kentucky, Sanders-Brown Center on Aging, Department of Physiology, Lexington, KY 40536, USA.
Neurodegener Dis Manag. 2013;3(4):343-351. doi: 10.2217/nmt.13.40.
There is currently no disease-modifying treatment for Alzheimer's disease (AD) and the need is great as the number of people diagnosed with AD is predicted to steadily increase. Inflammation is associated with AD, and is predictive of more advanced disease pathology and cognitive impairment. Moreover, preventing inflammation reduces the risk of developing AD. However, clinical trials with anti-inflammatory treatment have not been successful. One reason may be that there is diversity in the immune response and reducing immune activity with anti-inflammatories is not appropriate in all conditions. Recently, we have begun to apply categorizations, used to characterize the peripheral immune response, to the immune processes of the brain. When we do this, we are able to describe an individual's inflammatory profile within this spectrum. We have observed that patients with early AD are distributed across two broad categories of immune activation. If we recognize the diversity within this cohort of individuals with early AD and use information about immune phenotypes to guide the choice of treatment, then we may expect better clinical outcomes.
目前尚无针对阿尔茨海默病(AD)的疾病修饰治疗方法,而且由于预计被诊断为AD的人数将稳步增加,对此类治疗方法的需求非常迫切。炎症与AD相关,并且可预测更晚期的疾病病理和认知障碍。此外,预防炎症可降低患AD的风险。然而,抗炎治疗的临床试验尚未取得成功。一个原因可能是免疫反应存在多样性,在所有情况下使用抗炎药降低免疫活性并不合适。最近,我们已开始将用于表征外周免疫反应的分类方法应用于大脑的免疫过程。当我们这样做时,就能在此范围内描述个体的炎症特征。我们观察到,早期AD患者分布在两种广泛的免疫激活类别中。如果我们认识到这一早期AD患者群体中的多样性,并利用免疫表型信息来指导治疗选择,那么我们可能会期待更好的临床结果。