Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/48249
Title: The evolving landscape of Alzheimer's disease therapy: From AD to tau
Authors: Courade, Jean-Philippe
Zetterberg, Henrik
Hoglinger, Gunter U.
DEWACHTER, Ilse 
Issue Date: 2025
Publisher: CELL PRESS
Source: Cell, 188 (26) , p. 7337 -7354
Abstract: A marked evolution in Alzheimer's disease (AD) therapy research is ongoing. In this perspective, we highlight emerging outcomes of tau-targeting approaches with disease-modifying potential evidenced by PET-based slowing of tau accumulation and early signs of cognitive benefit. We outline how decades of iterative amyloid D (AD)-trial refinement leading to the recent successes of approved anti-AD therapies have set the stage for accelerated optimization of next-generation trials. We summarize key learnings from first-generation tau immunotherapies and how these paved the way for early achievements in tau trials, while many challenges remain. Finally, we discuss the back-translation of clinical outcomes into fundamental insights on human tau pathobiology, and we outline challenges and future directions for AD therapy development including combination therapy and targets beyond AD/tau. Together, this provides a framework for next-generation AD and tau-therapy development toward increasingly efficient disease-halting interventions.
Notes: Dewachter, I (corresponding author), Hasselt Univ, Biomed Res Inst BIOMED, Dept Neurosci, Hasselt, Belgium.
ilse.dewachter@uhasselt.be
Keywords: A(I)TN;ASO;AT(X)N;ATN;Abeta therapy;Alzheimer's disease;PET imaging;amyloid;anti-sense oligonucleotides;clinical trial;immunization;inflammation;neurodegeneration;next-generation therapies;tau;tau therapy;tauopathies;therapy development;trial;Humans;Immunotherapy;Animals;Clinical Trials as Topic;Alzheimer Disease;tau Proteins;Amyloid beta-Peptides
Document URI: http://hdl.handle.net/1942/48249
ISSN: 0092-8674
e-ISSN: 1097-4172
DOI: 10.1016/j.cell.2025.11.033
ISI #: 001653593600001
Rights: 2025 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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