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轻度认知障碍向阿尔茨海默病转化的免疫和影像学相关性。

Immune and Imaging Correlates of Mild Cognitive Impairment Conversion to Alzheimer's Disease.

机构信息

Laboratory of Molecular Medicine and Biotechnology, Don Gnocchi Foundation, IRCCS, Milan, Italy., Milan, Italy.

Department of Physiopathology and Transplants, University of Milano, 20100, Milan, Italy.

出版信息

Sci Rep. 2017 Dec 1;7(1):16760. doi: 10.1038/s41598-017-16754-y.

DOI:10.1038/s41598-017-16754-y
PMID:29196629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5711836/
Abstract

Amnestic mild cognitive impairment (aMCI) conversion to Alzheimer's disease (AD) is seen in a sizable portion of aMCI patients; correlates predicting such conversion are poorly defined but neuroinflammation and the reactivation of chronic viral infections are suspected to play a role in this phenomenon. We analyzed these aspects in two homogeneous groups of aMCI who did or did not convert to AD over a 24-months period. Results showed that at baseline in those aMCI individuals who did not convert to AD: 1) Aβ stimulated production of the pro-inflammatory cytokines IL6 and IL1β by CD14 cells was significantly reduced (p = 0.01), 2) CD14/IL-33 cells were increased (p = 0.0004); 3) MFI of TLR8 and TLR9 was significantly increased, and 4) better preserved hippocampus volumes were observed and correlated with IL33/CD14 cells. Notably, Aβ stimulated production of the antiviral cytokine IFN-λ was increased as well in non-AD converters, although with a borderline statistical significance (p = 0.05). Data herein indicating that proinflammatory cytokines are reduced, whereas IFN-λ production and TLR8 and 9 MFI are augmented in those aMCI in whom AD conversion is not observed suggest that the ability to mount stronger antiviral response within an antiiflammatory milieu associates with lack of AD conversion.

摘要

遗忘型轻度认知障碍 (aMCI) 向阿尔茨海默病 (AD) 的转化在相当一部分 aMCI 患者中可见;但预测这种转化的相关因素尚未明确,不过神经炎症和慢性病毒感染的再激活被怀疑在此现象中发挥作用。我们在两组同质的 aMCI 患者中分析了这些方面,这些患者在 24 个月的时间内分别发生或未发生向 AD 的转化。结果表明,在未向 AD 转化的 aMCI 个体中,基线时:1)Aβ 刺激 CD14 细胞产生促炎细胞因子 IL6 和 IL1β 的能力显著降低(p = 0.01);2)CD14/IL-33 细胞增加(p = 0.0004);3)TLR8 和 TLR9 的 MFI 显著增加;4)观察到海马体体积更好地保留,与 IL33/CD14 细胞相关。值得注意的是,非 AD 转化者中 Aβ 刺激抗病毒细胞因子 IFN-λ 的产生也增加,尽管具有统计学意义上的边缘显著性(p = 0.05)。数据表明,促炎细胞因子减少,而 IFN-λ 产生和 TLR8 和 9 的 MFI 增加,这表明在抗炎环境中能够产生更强的抗病毒反应与 AD 转化的缺失有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/5a7df909db37/41598_2017_16754_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/6d0c11d5606c/41598_2017_16754_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/c77cfd3cc724/41598_2017_16754_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/04cfab752f89/41598_2017_16754_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/5a7df909db37/41598_2017_16754_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/6d0c11d5606c/41598_2017_16754_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/c77cfd3cc724/41598_2017_16754_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/04cfab752f89/41598_2017_16754_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/089f/5711836/5a7df909db37/41598_2017_16754_Fig4_HTML.jpg

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