Tau-based therapeutics for Alzheimer's disease: active and passive immunotherapy

被引:63
作者
Panza, Francesco [1 ,2 ,3 ,4 ]
Solfrizzi, Vincenzo [5 ,6 ]
Seripa, Davide [3 ,4 ]
Imbimbo, Bruno P. [7 ]
Lozupone, Madia [1 ]
Santamato, Andrea [8 ]
Tortelli, Rosanna [1 ,2 ]
Galizia, Ilaria [9 ]
Prete, Camilla [10 ]
Daniele, Antonio [11 ]
Pilotto, Alberto [10 ]
Greco, Antonio [3 ,4 ]
Logroscino, Giancarlo [1 ,2 ,11 ]
机构
[1] Univ Bari Aldo Moro, Dept Basic Med Neurosci & Sense Organs, Neurodegenerat Dis Unit, Bari, Italy
[2] Univ Bari Aldo Moro, Pia Fdn Cardinale G Panico, Dept Clin Res Neurol, Lecce, Italy
[3] IRCCS Casa Sollievo Sofferenza, Geriatr Unit, Dept Med Sci, Foggia, Italy
[4] IRCCS Casa Sollievo Sofferenza, Lab Gerontol & Geriatr, Dept Med Sci, Foggia, Italy
[5] Univ Bari Aldo Moro, Geriatr Med Memory Unit, Bari, Italy
[6] Univ Bari Aldo Moro, Rare Dis Ctr, Bari, Italy
[7] Chiesi Farmaceut, Res & Dev Dept, Parma, Italy
[8] Univ Foggia, OORR Hosp, Phys Med & Rehabil Sect, Foggia, Italy
[9] Univ Bari Aldo Moro, Psychiat Unit, Dept Basic Med Neurosci & Sense Organs, Bari, Italy
[10] EO Galliera NR HS Hosp, Dept OrthoGeriatr Rehabil & Stabilizat, Frailty Area, Genoa, Italy
[11] Univ Cattolica Sacro Cuore, Inst Neurol, Rome, Italy
关键词
active immunotherapy; Alzheimer's disease; passive immunotherapy; AGGREGATION INHIBITOR THERAPY; MICROTUBULE-STABILIZING AGENT; PAIRED HELICAL FILAMENTS; PROTEIN PHOSPHATASE 2A; MOUSE MODEL; STRUCTURAL DETERMINANTS; HYPERPHOSPHORYLATED-TAU; AMYLOID-BETA; A-BETA; NEUROFIBRILLARY DEGENERATION;
D O I
10.2217/imt-2016-0019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pharmacological manipulation of tau protein in Alzheimer's disease included microtubule-stabilizing agents, tau protein kinase inhibitors, tau aggregation inhibitors, active and passive immunotherapies and, more recently, inhibitors of tau acetylation. Animal studies have shown that both active and passive approaches can remove tau pathology and, in some cases, improve cognitive function. Two active vaccines targeting either nonphosphorylated (AAD-vac1) and phosphorylated tau (ACI-35) have entered Phase I testing. Notwithstanding, the recent discontinuation of the monoclonal antibody RG7345 for Alzheimer's disease, two other antitau antibodies, BMS-986168 and C2N-8E12, are also currently in Phase I testing for progressive supranuclear palsy. After the recent impressive results in animal studies obtained by salsalate, the dimer of salicylic acid, inhibitors of tau acetylation are being actively pursued.
引用
收藏
页码:1119 / 1134
页数:16
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