Targeting tau: Clinical trials and novel therapeutic approaches

L VandeVrede, AL Boxer, M Polydoro - Neuroscience letters, 2020 - Elsevier
L VandeVrede, AL Boxer, M Polydoro
Neuroscience letters, 2020Elsevier
Tauopathies are a group of over 20 clinicopathological neurodegenerative diseases
including Alzheimer's disease (AD), the most common type of dementia, progressive
supranuclear palsy, Pick's disease, corticobasal degeneration, among others. Tauopathies
are defined by neurodegeneration and the presence of tau aggregates in affected brains
regions. Interestingly, regional tau aggregation burden correlates with clinical phenotype
and predicts cognitive status. Autosomal dominant mutations in the MAPT gene lead to tau …
Abstract
Tauopathies are a group of over 20 clinicopathological neurodegenerative diseases including Alzheimer's disease (AD), the most common type of dementia, progressive supranuclear palsy, Pick's disease, corticobasal degeneration, among others. Tauopathies are defined by neurodegeneration and the presence of tau aggregates in affected brains regions. Interestingly, regional tau aggregation burden correlates with clinical phenotype and predicts cognitive status. Autosomal dominant mutations in the MAPT gene lead to tau deposition and clinical FTD syndromes with cognitive, behavioral, and motor impairment. Polymorphisms in or around the MAPT gene have also been strongly linked to other proteinopathies including synucleinopathies. Taken together these findings suggests that tau plays a critical role in neurodegeneration and proteinopathies, supporting the idea that tau targeted approaches can be disease-modifying and lead to clinically meaningful benefits in slowing or reversing disease progression. Increasingly, human clinical trials are testing this hypothesis. This article reviews tau-targeted therapies tested in clinical trials as well as agents currently in active development based on publicly disclosed information. We describe the therapeutic approaches of these trials based on the potential pathogenic mechanism they target.
Elsevier