Brain endothelial cell-targeted gene therapy of neurovascular disorders

Serena Marchiò, Richard L. Sidman, Wadih Arap, Renata Pasqualini

Research output: Contribution to journalArticle

4 Scopus citations


Neurovascular disorders are difficult to treat due to the blood-brain barrier (BBB), which prevents delivery of most drugs from the blood into the brain. Gene therapy can potentially overcome this barrier, but classical vectors are neither efficient nor specific enough to provide long-lasting treatment or avoid off-target effects. In this issue of EMBO Molecular Medicine, Körbelin et al describe an engineered adeno-associated virus (AAV) with exceptional tropism for the brain that restores a normal phenotype in a mouse model of incontinentia pigmenti (IP), a severe human genetic disorder of brain vasculature.

Original languageEnglish (US)
Pages (from-to)592-594
Number of pages3
JournalEMBO Molecular Medicine
Issue number6
StatePublished - Jun 1 2016
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Molecular Medicine

Fingerprint Dive into the research topics of 'Brain endothelial cell-targeted gene therapy of neurovascular disorders'. Together they form a unique fingerprint.

  • Cite this