Affiliations 

  • 1 Molecular Neurogenetics Unit, Department of Neurology, The Massachusetts General Hospital, Charlestown MA and Program in Neuroscience, Harvard Medical School, Boston, MA, USA
  • 2 Surgical Photonics & Engineering Laboratory, Mass Eye and Ear, Harvard Medical School, Boston, MA, 02114, USA
  • 3 Department of Medicine, Harvard Medical School, Boston, MA, 02215, USA
  • 4 Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA
  • 5 Molecular Neurogenetics Unit, Department of Neurology, The Massachusetts General Hospital, Charlestown MA and Program in Neuroscience, Harvard Medical School, Boston, MA, USA. breakefield@hms.harvard.edu
  • 6 Molecular Neurogenetics Unit, Department of Neurology, The Massachusetts General Hospital, Charlestown MA and Program in Neuroscience, Harvard Medical School, Boston, MA, USA. cmaguire@mgh.harvard.edu
Gene Ther, 2025 Jul;32(4):385-397.
PMID: 40494929 DOI: 10.1038/s41434-025-00542-9

Abstract

Genetic diseases such as Neurofibromatosis type 1 (NF1) and Charcot-Marie Tooth disease involve Schwann cells (SCs) associated with peripheral nerves. Gene therapy using adeno-associated virus (AAV) vector mediated gene delivery is a promising strategy to treat these diseases. However, AAV-mediated transduction of SCs in vivo after intravascular delivery is relatively inefficient, with a lack of extensive characterization of different capsids to date. Here, we performed an in vivo selection with an AAV9 capsid peptide display library in a mouse model of NF1. We chose one capsid variant, AAV-SC3, which was present in NF1 nerves for comparison to two benchmark capsids after systemic injection. AAV-SC3 significantly outperformed one of the two benchmark capsids at levels of transgene mRNA in the neurofibroma. Immunofluorescence microscopy revealed transgene expressing Sox10-positive SCs throughout the neurofibroma with AAV-SC3 injection. Next, we performed a pooled screen with four of the top capsids from our initial selection and AAV9 and identified one capsid, AAV-SC4, with enhanced biodistribution to and transduction of normal sciatic nerve in mice. This capsid displayed a peptide with a known laminin-binding motif, which may provide a conduit for future laminin-targeting strategies. Our results provide a baseline for future AAV-based gene therapies developed for NF1 or other diseases that affect SCs.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.