| Literature DB >> 35915232 |
Xumeng Hu1, Beibei Zhang1, Xiaoli Li1, Miao Li1, Yange Wang1, Handong Dan1, Jiamu Zhou1, Yuanmeng Wei1, Keke Ge1, Pan Li1, Zongming Song2.
Abstract
The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated nuclease (Cas) system is an adaptive immune defence system that has gradually evolved in bacteria and archaea to combat invading viruses and exogenous DNA. Advances in technology have enabled researchers to enhance their understanding of the immune process in vivo and its potential for use in genome editing. Thus far, applications of CRISPR/Cas9 genome editing technology in ophthalmology have included gene therapy for corneal dystrophy, glaucoma, congenital cataract, Leber's congenital amaurosis, retinitis pigmentosa, Usher syndrome, fundus neovascular disease, proliferative vitreoretinopathy, retinoblastoma and other eye diseases. Additionally, the combination of CRISPR/Cas9 genome editing technology with adeno-associated virus vector and inducible pluripotent stem cells provides further therapeutic avenues for the treatment of eye diseases. Nonetheless, many challenges remain in the development of clinically feasible retinal genome editing therapy. This review discusses the development, as well as mechanism of CRISPR/Cas9 and its applications and challenges in gene therapy for eye diseases.Entities:
Year: 2022 PMID: 35915232 DOI: 10.1038/s41433-022-02169-1
Source DB: PubMed Journal: Eye (Lond) ISSN: 0950-222X Impact factor: 4.456