Clinical applications of retinal gene therapies

Precis Clin Med. 2018 Jun;1(1):5-20. doi: 10.1093/pcmedi/pby004. Epub 2018 Jun 1.

Abstract

Retinal degenerative diseases are a major cause of blindness. Retinal gene therapy is a trail-blazer in the human gene therapy field, leading to the first FDA approved gene therapy product for a human genetic disease. The application of Clustered Regularly Interspaced Short Palindromic Repeat/Cas9 (CRISPR/Cas9)-mediated gene editing technology is transforming the delivery of gene therapy. We review the history, present, and future prospects of retinal gene therapy.

Publication types

  • Review