Asselineau Delphine, Benlhassan Khadija, Arosio Beatrice, Mari Daniela, Ferri Evelyn, Casati Martina, Gussago Cristina, Tedone Enzo, Annoni Giorgio, Mazzola Paolo, Piette Francois, Belmin Joel, Pariel Sylvie, Bornand Anne, Beaudeux Jean-Louis, Doulazmi Mohamed, Mariani Jean, Bray Dorothy H
ImmunoClin Ltd, London, UK.
UPMC University Paris 06, UMR 8256 Biological Adaptation and Ageing (B2A) Team Brain Development, Repair and Aging (BDRA), Paris, France.
J Alzheimers Dis. 2015;46(4):837-42. doi: 10.3233/JAD-142832.
We investigated IL-10 and IL-6 production in amyloid-β (Aβ) stimulated peripheral blood mononuclear cells (PBMCs) in twenty Alzheimer's disease (AD) patients with slow progression, eleven with fast progression, and twenty age-matched controls. Promoter polymorphisms in IL-10 (position -592, -819, -1082), IL-6 (-174), transforming growth factor-β1 (TGF-β1) (-10, -25), interferon-γ (IFN-γ) (-874), and tumor necrosis factor-α (TNF-α) (-308) genes were analyzed. IL-10 production after Aβ stimulation was high in PBMCs from slow decliners and almost completely abrogated in fast decliners. Association between AA IFN-γ low-producing genotype and fast progression was demonstrated. Investigations in a larger sample will clarify these findings.
我们研究了20例病情进展缓慢的阿尔茨海默病(AD)患者、11例病情进展快速的患者以及20例年龄匹配的对照者中,淀粉样β蛋白(Aβ)刺激外周血单个核细胞(PBMCs)后白细胞介素-10(IL-10)和白细胞介素-6的产生情况。分析了IL-10(-592、-819、-1082位点)、IL-6(-174位点)、转化生长因子-β1(TGF-β1)(-10、-25位点)、干扰素-γ(IFN-γ)(-874位点)和肿瘤坏死因子-α(TNF-α)(-308位点)基因的启动子多态性。Aβ刺激后,病情进展缓慢者的PBMCs中IL-10产生量较高,而病情进展快速者几乎完全消失。证实了AA型IFN-γ低产生基因型与快速进展之间的关联。在更大样本中的研究将阐明这些发现。