Söllvander Sofia, Ekholm-Pettersson Frida, Brundin Rose-Marie, Westman Gabriel, Kilander Lena, Paulie Staffan, Lannfelt Lars, Sehlin Dag
Department of Public Health & Caring Sciences/Molecular Geriatrics, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
J Alzheimers Dis. 2015;48(1):63-72. doi: 10.3233/JAD-150236.
The Alzheimer's disease (AD)-related peptide amyloid-β (Aβ) has a propensity to aggregate into various assemblies including toxic soluble Aβ protofibrils. Several studies have reported the existence of anti-Aβ antibodies in humans. However, it is still debated whether levels of anti-Aβ antibodies are altered in AD patients compared to healthy individuals. Formation of immune complexes with plasma Aβ makes it difficult to reliably measure the concentration of circulating anti-Aβ antibodies with certain immunoassays, potentially leading to an underestimation. Here we have investigated anti-Aβ antibody production on a cellular level by measuring the amount of anti-Aβ antibody producing cells instead of the plasma level of anti-Aβ antibodies. To our knowledge, this is the first time the anti-Aβ antibody response in plasma has been compared in AD patients and age-matched healthy individuals using the enzyme-linked immunospot (ELISpot) technique. Both AD patients and healthy individuals had low levels of B cells producing antibodies binding Aβ40 monomers, whereas the number of cells producing antibodies toward Aβ42 protofibrils was higher overall and significantly higher in AD compared to healthy controls. This study shows, by an alternative and reliable method, that there is a specific immune response to the toxic Aβ protofibrils, which is significantly increased in AD patients.
与阿尔茨海默病(AD)相关的肽淀粉样β蛋白(Aβ)易于聚集成包括有毒可溶性Aβ原纤维在内的各种聚集体。多项研究报告了人类体内存在抗Aβ抗体。然而,与健康个体相比,AD患者体内抗Aβ抗体水平是否发生改变仍存在争议。与血浆Aβ形成免疫复合物使得通过某些免疫测定法可靠地测量循环抗Aβ抗体的浓度变得困难,这可能导致低估。在此,我们通过测量产生抗Aβ抗体的细胞数量而非抗Aβ抗体的血浆水平,在细胞水平上研究了抗Aβ抗体的产生。据我们所知,这是首次使用酶联免疫斑点(ELISpot)技术比较AD患者和年龄匹配的健康个体血浆中的抗Aβ抗体反应。AD患者和健康个体产生结合Aβ40单体抗体的B细胞水平均较低,而产生针对Aβ42原纤维抗体的细胞数量总体上更高,且与健康对照相比,AD患者中的该细胞数量显著更高。这项研究通过一种替代且可靠的方法表明,对有毒Aβ原纤维存在特异性免疫反应,且在AD患者中显著增强。