Yanamandra Kiran, Patel Tirth K, Jiang Hong, Schindler Suzanne, Ulrich Jason D, Boxer Adam L, Miller Bruce L, Kerwin Diana R, Gallardo Gilbert, Stewart Floy, Finn Mary Beth, Cairns Nigel J, Verghese Philip B, Fogelman Ilana, West Tim, Braunstein Joel, Robinson Grace, Keyser Jennifer, Roh Joseph, Knapik Stephanie S, Hu Yan, Holtzman David M
Hope Center for Neurological Disorders and Knight Alzheimer's Disease Research Center, Department of Neurology, Washington University, St. Louis, MO 63110,USA.
AbbVie Inc. Foundational Neuroscience Center, Cambridge, MA 02139, USA.
Sci Transl Med. 2017 Apr 19;9(386). doi: 10.1126/scitranslmed.aal2029.
Tauopathies are a group of disorders in which the cytosolic protein tau aggregates and accumulates in cells within the brain, resulting in neurodegeneration. A promising treatment being explored for tauopathies is passive immunization with anti-tau antibodies. We previously found that administration of an anti-tau antibody to human tau transgenic mice increased the concentration of plasma tau. We further explored the effects of administering an anti-tau antibody on plasma tau. After peripheral administration of an anti-tau antibody to human patients with tauopathy and to mice expressing human tau in the central nervous system, there was a dose-dependent increase in plasma tau. In mouse plasma, we found that tau had a short half-life of 8 min that increased to more than 3 hours after administration of anti-tau antibody. As tau transgenic mice accumulated insoluble tau in the brain, brain soluble and interstitial fluid tau decreased. Administration of anti-tau antibody to tau transgenic mice that had decreased brain soluble tau and interstitial fluid tau resulted in an increase in plasma tau, but this increase was less than that observed in tau transgenic mice without these brain changes. Tau transgenic mice subjected to acute neuronal injury using 3-nitropropionic acid showed increased interstitial fluid tau and plasma tau. These data suggest that peripheral administration of an anti-tau antibody results in increased plasma tau, which correlates with the concentration of extracellular and soluble tau in the brain.
tau蛋白病是一组疾病,其中细胞溶质蛋白tau在脑内细胞中聚集和积累,导致神经退行性变。正在探索的一种有前景的tau蛋白病治疗方法是用抗tau抗体进行被动免疫。我们之前发现,给人tau转基因小鼠施用抗tau抗体可增加血浆tau的浓度。我们进一步探讨了施用抗tau抗体对血浆tau的影响。在给患有tau蛋白病的人类患者和在中枢神经系统中表达人tau的小鼠外周施用抗tau抗体后,血浆tau呈剂量依赖性增加。在小鼠血浆中,我们发现tau的半衰期较短,为8分钟,施用抗tau抗体后增加到3小时以上。由于tau转基因小鼠在脑中积累了不溶性tau,脑可溶性和间质液tau减少。给脑可溶性tau和间质液tau减少的tau转基因小鼠施用抗tau抗体导致血浆tau增加,但这种增加小于在没有这些脑变化的tau转基因小鼠中观察到的增加。使用3-硝基丙酸对tau转基因小鼠进行急性神经元损伤后,间质液tau和血浆tau增加。这些数据表明,外周施用抗tau抗体导致血浆tau增加,这与脑中细胞外和可溶性tau的浓度相关。