Larbi Anis, Pawelec Graham, Witkowski Jacek M, Schipper Hyman M, Derhovanessian Evelyna, Goldeck David, Fulop Tamas
Center for Medical Research, University of Tübingen, Tübingen, Germany.
J Alzheimers Dis. 2009;17(1):91-103. doi: 10.3233/JAD-2009-1015.
The distribution of peripheral T cell subsets in young and healthy old people is markedly different, characterized by decreased numbers of naïve cells and increased numbers and clonal expansions of memory cells, predominantly in the CD8+ MHC class I-restricted subset. Here, however, we document dramatic alterations in naïve and memory subsets of CD4+ cells in patients with mild Alzheimer's disease (AD), with greatly decreased percentages of naïve cells, elevated memory cells, and increased proportions of CD4+ but not CD8+ cells lacking the important costimulatory receptor CD28. CD4+CD25(high) potentially T regulatory cells with a naïve phenotype are also reduced in AD patients. Together these data provide stronger evidence than hitherto presented for more highly differentiated CD4+ as well as CD8+ T cells in AD patients, consistent with an adaptive immune system undergoing persistent antigenic challenge and possibly manifesting dysregulation as a result.
年轻健康老人与老年人外周血T细胞亚群的分布显著不同,其特征为初始细胞数量减少,记忆细胞数量增加且出现克隆性扩增,主要发生在CD8⁺MHC I类限制性亚群中。然而,在此我们记录了轻度阿尔茨海默病(AD)患者CD4⁺细胞的初始和记忆亚群发生的显著变化,初始细胞百分比大幅降低,记忆细胞升高,且缺乏重要共刺激受体CD28的CD4⁺而非CD8⁺细胞比例增加。AD患者中具有初始表型的CD4⁺CD25(高)潜在调节性T细胞也减少。这些数据共同提供了比以往更强的证据,表明AD患者中CD4⁺以及CD8⁺T细胞具有更高的分化程度,这与适应性免疫系统持续受到抗原刺激并可能因此出现失调相一致。