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首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >Differential neuroimmune markers to the onset of Alzheimer's disease neurodegeneration and dementia: Autoantibodies to Abeta((25-35)) oligomers, S100b and neurotransmitters.
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Differential neuroimmune markers to the onset of Alzheimer's disease neurodegeneration and dementia: Autoantibodies to Abeta((25-35)) oligomers, S100b and neurotransmitters.

机译:阿尔茨海默氏病神经变性和痴呆发作的差异性神经免疫标志物:Abeta((25-35))低聚物,S100b和神经递质的自身抗体。

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摘要

Alzheimer's disease (AD) autoimmunity is a focus for dementia prevention. Generated autoantibodies against major etiopathogenic molecular targets as neuroimmune markers of dementia were measured by ELISA in patient sera. Biphasic antibody levels to Abeta((25-35)) oligomers, S100b and DA were detected during distinctly diagnosed dementia stages. Abeta((25-35)) oligomer autoimmune responses reflected mild to moderate AD dementia, while those to S100b, DA and the S100b concentrations, matched moderate to severe dementia progression. 5-HT antibodies increased during mild dementia and plateaued thereafter. This autoimmunity pattern may be used as a differential biomarker profile in designing AD therapeutic strategies involving early vaccination.
机译:阿尔茨海默氏病(AD)自身免疫是预防痴呆症的重点。通过ELISA在患者血清中测量针对主要病原性分子靶标(作为痴呆症的神经免疫标志物)的自身抗体。在明确诊断的痴呆阶段中检测到针对Abeta((25-35))低聚物,S100b和DA的双相抗体水平。 Abeta((25-35))低聚物自身免疫反应反映轻度至中度AD痴呆,而那些针对S100b,DA和S100b浓度的痴呆进展与中度至重度痴呆发展相匹配。 5-HT抗体在轻度痴呆期间增加,此后趋于稳定。在设计涉及早期疫苗接种的AD治疗策略时,这种自身免疫模式可以用作差异生物标志物。

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