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

Author:

Panza Francesco123,Solfrizzi Vincenzo4,Seripa Davide3,Imbimbo Bruno P5,Lozupone Madia1,Santamato Andrea6,Tortelli Rosanna12,Galizia Ilaria7,Prete Camilla8,Daniele Antonio9,Pilotto Alberto8,Greco Antonio3,Logroscino Giancarlo129

Affiliation:

1. Neurodegenerative Disease Unit, Department of Basic Medicine, Neuroscience, & Sense Organs, University of Bari Aldo Moro, Bari, Italy

2. Department of Clinical Research in Neurology, University of Bari Aldo Moro, ‘Pia Fondazione Cardinale G. Panico,’ Tricase, Lecce, Italy

3. Geriatric Unit & Laboratory of Gerontology & Geriatrics, Department of Medical Sciences, IRCCS ‘Casa Sollievo della Sofferenza,’ San Giovanni Rotondo, Foggia, Italy

4. Geriatric Medicine-Memory Unit & Rare Disease Centre, University of Bari Aldo Moro, Bari, Italy

5. Research & Development Department, Chiesi Farmaceutici, Parma, Italy

6. Physical Medicine & Rehabilitation Section, ‘OORR’ Hospital, University of Foggia, Foggia, Italy

7. Psychiatric Unit, Department of Basic Medicine, Neuroscience, & Sense Organs, University of Bari Aldo Moro, Bari, Italy

8. Department of OrthoGeriatrics, Rehabilitation & Stabilization, Frailty Area, E.O. Galliera NR-HS Hospital, Genova, Italy

9. Institute of Neurology, Catholic University of Sacred Heart, Rome, Italy

Abstract

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.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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