Efficient targeting of human glial progenitor cells in vivo with engineered AAV vectors and glymphatic delivery

Read full text
Authors: Alexander Cona, Evan Newbold, Deniz Kesmen, Rajiv Snape, Jessica Danner, Nicholas White, William Borden, Abigail Iseson, Steven J. Schanz, Devin Chandler-Militello, X Li, Jose C. Cano
+4 more John N. Mariani, Maiken Nedergaard, Abdellatif Benraiss, Steven A. Goldman
Cited by: 1
References: 58

Abstract

Treatment of neurological diseases that involve oligodendrocytes or astrocytes would benefit from the selective delivery of viral vectors to their common parent, glial progenitor cells (GPCs). Here, we select adeno-associated virus (AAV) capsids with tropism for human GPCs and demonstrate efficient and widespread delivery of the resultant AAVs throughout the mouse brain through the glymphatic system. In vivo screening of a library of capsid-modified, recombination-reported AAVs in chimeric mice engrafted with PDGFRA-driven Cre recombinase-expressing human GPCs identified a set of AAV5-based vectors that preferentially infect human GPCs and/or their astrocyte and oligodendrocyte progeny in vivo, with minimal systemic infection. To maximize the intracerebral distribution of these vectors while minimizing their dosing and extracerebral spread, we paired intracisternal delivery with systemic hypertonicity to increase glymphatic influx. This method bypasses the blood-brain barrier, delivering AAV directly into the brain parenchyma. Glymphatic delivery of our capsid-modified AAV5s enables efficient transgene delivery to human glia throughout the entire adult mouse brain, with minimal off-target transduction.

Fields of Study & Subjects

Cerebrospinal fluid and hydrocephalus Virus-based gene therapy research Neurogenesis and neuroplasticity mechanisms

Publication details

Journal / source
Nature Biotechnology
Publisher
Springer Science and Business Media LLC
Publication date
8 July 2026
Language
EN