From the Department of Aging Neurobiology, Center for Development of Advanced Medicine for Dementia, National Center for Geriatrics and Gerontology, Obu, Aichi, Japan.
Department of Aging Neurobiology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
J Neuropathol Exp Neurol. 2021 Aug 11;80(7):652-662. doi: 10.1093/jnen/nlab047.
Despite the routine use of sandwich enzyme-linked immunosorbent assays (ELISAs) for quantifying tau levels in CSF and plasma, tau accumulations in the brains of patients with Alzheimer disease (AD) have rarely been evaluated by this method. Thus, by introducing several tau ELISAs that target different epitopes, we evaluated accumulated tau levels in postmortem brains depending on disease stage, brain areas, and other AD-related changes. Notably, tau levels in insoluble fraction determined by each ELISAs differ depending on the epitopes of antibodies: non-AD control samples yield relatively high signals when an antibody against the N-terminal region of tau is used. On the other hand, ELISAs combining antibodies against the later-middle to C-terminal regions of tau produced substantially increased signals from AD samples, compared to those from non-AD controls. Such ELISAs better distinguish AD and non-AD controls, and the results are more closely associated with Braak neurofibrillary tangles stage, Aβ accumulation, and glial markers. Moreover, these ELISAs can reflect the pattern of tau spread across brain regions. In conclusion, Tau ELISAs that combine antibodies against the later-middle to C-terminal regions of tau can better reflect neuropathological tau accumulation, which would enable to evaluate tau accumulation in the brain at a biochemical level.
尽管夹心酶联免疫吸附测定(ELISA)常用于定量 CSF 和血浆中的 tau 水平,但这种方法很少用于评估阿尔茨海默病(AD)患者大脑中的 tau 堆积。因此,通过引入几种针对不同表位的 tau ELISA,我们根据疾病阶段、脑区和其他与 AD 相关的变化来评估死后大脑中的 tau 积累水平。值得注意的是,每种 ELISA 测定的不溶性部分的 tau 水平因抗体的表位而异:当使用针对 tau N 端区域的抗体时,非 AD 对照样本会产生相对较高的信号。另一方面,与非 AD 对照相比,针对 tau 中-后段到 C 端的抗体组合的 ELISA 从 AD 样本中产生了显著增加的信号。这些 ELISA 可以更好地区分 AD 和非 AD 对照,并且结果与 Braak 神经原纤维缠结阶段、Aβ 积累和神经胶质标志物更密切相关。此外,这些 ELISA 可以反映 tau 在脑区之间的传播模式。总之,针对 tau 中-后段到 C 端的抗体组合的 Tau ELISA 可以更好地反映神经病理学 tau 积累,这将能够在生化水平上评估大脑中的 tau 积累。