Affiliation:
1. Department of Radiotherapy and Translational Medicine Center Huaihe Hospital of Henan University Henan University Kaifeng Henan 475000 China
2. Henan‐Macquarie University Joint Centre for Biomedical Innovation School of Life Sciences Henan University Kaifeng Henan 475004 China
3. Macquarie Medical School Faculty of Medicine & Health Sciences Macquarie University Sydney New South Wales 2109 Australia
Abstract
AbstractAlzheimer's disease (AD) is the most burdensome aging‐associated neurodegenerative disorder, and its treatment encounters numerous failures during drug development. Although there are newly approved in‐market β‐amyloid targeting antibody solutions, pathological heterogeneity among patient populations still challenges the treatment outcome. Emerging advances in gene therapies offer opportunities for more precise personalized medicine; while, major obstacles including the pathological heterogeneity among patient populations, the puzzled mechanism for druggable target development, and the precision delivery of functional therapeutic elements across the blood–brain barrier remain and limit the use of gene therapy for central neuronal diseases. Aiming for “precision delivery” challenges, nanomedicine provides versatile platforms that may overcome the targeted delivery challenges for AD gene therapy. In this perspective, to picture a toolbox for AD gene therapy strategy development, the most recent advances from benchtop to clinics are highlighted, possibly available gene therapy targets, tools, and delivery platforms are outlined, their challenges as well as rational design elements are addressed, and perspectives in this promising research field are discussed.
Funder
National Health and Medical Research Council
Science and Technology Innovation Talents in Universities of Henan Province
Postdoctoral Science Foundation of Jiangsu Province
National Outstanding Youth Science Fund Project of National Natural Science Foundation of China