生物
疾病
集合(抽象数据类型)
认知
神经科学
钥匙(锁)
复杂疾病
生物信息学
计算生物学
工程伦理学
数据科学
人类疾病
认识论
淀粉样β
认知科学
作者
Jean‐Philippe Courade,Henrik Zetterberg,Günter U. Höglinger,Ilse Dewachter
出处
期刊:Cell
[Cell Press]
日期:2025-12-01
卷期号:188 (26): 7337-7354
被引量:8
标识
DOI:10.1016/j.cell.2025.11.033
摘要
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 β (Aβ)-trial refinement leading to the recent successes of approved anti-Aβ 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 Aβ/tau. Together, this provides a framework for next-generation AD and tau-therapy development toward increasingly efficient disease-halting interventions.
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