» Articles » PMID: 34722588

Gene Therapy in Inherited Retinal Diseases: An Update on Current State of the Art

Overview
Specialty General Medicine
Date 2021 Nov 1
PMID 34722588
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Gene therapy cannot be yet considered a far perspective, but a tangible therapeutic option in the field of retinal diseases. Although still confined in experimental settings, the preliminary results are promising and provide an overall scenario suggesting that we are not so far from the application of gene therapy in clinical settings. The main aim of this review is to provide a complete and updated overview of the current state of the art and of the future perspectives of gene therapy applied on retinal diseases. We carefully revised the entire literature to report all the relevant findings related to the experimental procedures and the future scenarios of gene therapy applied in retinal diseases. A clinical background and a detailed description of the genetic features of each retinal disease included are also reported. The current literature strongly support the hope of gene therapy options developed for retinal diseases. Although being considered in advanced stages of investigation for some retinal diseases, such as choroideremia (CHM), retinitis pigmentosa (RP), and Leber's congenital amaurosis (LCA), gene therapy is still quite far from a tangible application in clinical practice for other retinal diseases. Gene therapy is an extremely promising therapeutic tool for retinal diseases. The experimental data reported in this review offer a strong hope that gene therapy will be effectively available in clinical practice in the next years.

Citing Articles

Retinal Inflammation and Reactive Müller Cells: Neurotrophins' Release and Neuroprotective Strategies.

Balzamino B, Cacciamani A, Dinice L, Cecere M, Pesci F, Ripandelli G Biology (Basel). 2025; 13(12.

PMID: 39765697 PMC: 11673524. DOI: 10.3390/biology13121030.


dCasMINI-mediated therapy rescues photoreceptors degeneration in a mouse model of retinitis pigmentosa.

Wang Q, Xu X, Chen S, Lu R, Li L, Lo C Sci Adv. 2024; 10(51):eadn7540.

PMID: 39693439 PMC: 11654696. DOI: 10.1126/sciadv.adn7540.


Bridging the gap of vision restoration.

Carleton M, Oesch N Front Cell Neurosci. 2024; 18:1502473.

PMID: 39640234 PMC: 11617155. DOI: 10.3389/fncel.2024.1502473.


Advances and Challenges in Gene Therapy for Inherited Retinal Dystrophies: A Comprehensive Review.

Jain R, Daigavane S Cureus. 2024; 16(9):e69895.

PMID: 39439625 PMC: 11494405. DOI: 10.7759/cureus.69895.


Advances in retina genetics: Progress, potential, and challenges.

Bansal M Indian J Ophthalmol. 2024; 73(Suppl 1):S31-S36.

PMID: 39257094 PMC: 11834934. DOI: 10.4103/IJO.IJO_3334_23.


References
1.
OReilly M, Palfi A, Chadderton N, Millington-Ward S, Ader M, Cronin T . RNA interference-mediated suppression and replacement of human rhodopsin in vivo. Am J Hum Genet. 2007; 81(1):127-35. PMC: 1950918. DOI: 10.1086/519025. View

2.
Mandelcorn E, Kitchens J, Fijalkowski N, Moshfeghi D . Active aspiration of suprachoroidal hemorrhage using a guarded needle. Ophthalmic Surg Lasers Imaging Retina. 2014; 45(2):150-2. DOI: 10.3928/23258160-20140306-09. View

3.
Berger W, Kloeckener-Gruissem B, Neidhardt J . The molecular basis of human retinal and vitreoretinal diseases. Prog Retin Eye Res. 2010; 29(5):335-75. DOI: 10.1016/j.preteyeres.2010.03.004. View

4.
Hauswirth W, Lewin A . Ribozyme uses in retinal gene therapy. Prog Retin Eye Res. 2000; 19(6):689-710. DOI: 10.1016/s1350-9462(00)00007-0. View

5.
Maeder M, Stefanidakis M, Wilson C, Baral R, Barrera L, Bounoutas G . Development of a gene-editing approach to restore vision loss in Leber congenital amaurosis type 10. Nat Med. 2019; 25(2):229-233. DOI: 10.1038/s41591-018-0327-9. View