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Immune responses in rapidly progressive dementia: a comparative study of neuroinflammatory markers in Creutzfeldt-Jakob disease Alzheimer’s disease and multiple sclerosis

机译:快速进展性痴呆的免疫反应:克雅氏病阿尔茨海默氏病和多发性硬化症中神经炎症标记物的比较研究

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摘要

Immunological responses may contribute to disease progression and clinical heterogeneity in neurodegenerative dementia, for example, Alzheimer’s disease (AD) and Creutzfeldt-Jakob disease (CJD). Recently, a rapidly progressive form of AD (rpAD) has been described. On neuropathological grounds classical AD and rpAD are not distinguishable at present. All those protein aggregopathies show a state of chronic inflammation with microglia activation and production of proinflammatory cytokines. In this context, it is hypothesized that the severity of the surrounding inflammation substantially contributes to disease progression and accelerated disease courses as seen in rpAD.Using a cytokine multiplex array based on Luminex Technology, we studied 17 pro- and anti-inflammatory cytokines in cerebrospinal fluid (CSF) and serum from patients with classical dementia (AD) or rapidly progressive dementia (Creutzfeldt-Jakob disease (CJD), rpAD). For controls, we chose patients with multiple sclerosis (MS) and non-neurodegenerative diseases. We found a significant and isolated elevation of proinflammatory cytokines (IL-13, TNF-α and G-CSF) in the serum of rpAD patients. In CSF, IL-8 and MCP-1 chemokines were significantly elevated in CJD patients and MCP-1 in AD patients.In conclusion, we found a characteristic proinflammatory cytokine response in the serum of rpAD patients. It might explain the more rapidly progressive course of the rpAD subform and can be helpful in distinguishing between classical AD and rpAD.Electronic supplementary materialThe online version of this article (doi:10.1186/s12974-014-0170-y) contains supplementary material, which is available to authorized users.
机译:免疫学反应可能会导致神经退行性痴呆的疾病进展和临床异质性,例如阿尔茨海默氏病(AD)和克雅氏病(CJD)。最近,已经描述了AD的快速发展形式(rpAD)。在神经病理学方面,目前尚不能区分经典AD和rpAD。所有这些蛋白聚集反应均显示出具有小胶质细胞活化和促炎细胞因子产生的慢性炎症状态。在这种情况下,假设周围炎症的严重性极大地促进了疾病进展和疾病进程的加速,如rpAD所示。使用基于Luminex Technology的细胞因子多重阵列,我们研究了脑脊髓中的17种促炎和抗炎细胞因子患有经典痴呆(AD)或快速进行性痴呆(Creutzfeldt-Jakob病(CJD),rpAD)的患者的体液(CSF)和血清。作为对照,我们选择患有多发性硬化症(MS)和非神经退行性疾病的患者。我们发现rpAD患者血清中促炎细胞因子(IL-13,TNF-α和G-CSF)显着升高。在CSF中,CJD患者的IL-8和MCP-1趋化因子显着升高,AD患者的MCP-1显着升高。总之,我们在rpAD患者的血清中发现了特征性的促炎细胞因子反应。它可能解释了rpAD子窗体的快速发展过程,并有助于区分经典AD和rpAD。电子补充材料本文的在线版本(doi:10.1186 / s12974-014-0170-y)包含补充材料,其中适用于授权用户。

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