In Vivo and Ex Vivo Gene Electrotransfer in Ophthalmological Disorders

The aim of this document is to present an overview of gene electrotransfer in ophthalmological disorders. In order to ensure an adequate variety of the assessed studies, several electronic databases were considered and studies published between January 1998 and December 2021 were analysed. Three inv...

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Main Authors: Roberta Fusco, Giacomo Perazzolo Gallo, Elio Di Bernardo, Valeria D’Alessio, Mattia Ronchetti, Matteo Cadossi, Ruggero Cadossi
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/10/8/1889
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author Roberta Fusco
Giacomo Perazzolo Gallo
Elio Di Bernardo
Valeria D’Alessio
Mattia Ronchetti
Matteo Cadossi
Ruggero Cadossi
author_facet Roberta Fusco
Giacomo Perazzolo Gallo
Elio Di Bernardo
Valeria D’Alessio
Mattia Ronchetti
Matteo Cadossi
Ruggero Cadossi
author_sort Roberta Fusco
collection DOAJ
description The aim of this document is to present an overview of gene electrotransfer in ophthalmological disorders. In order to ensure an adequate variety of the assessed studies, several electronic databases were considered and studies published between January 1998 and December 2021 were analysed. Three investigators carried out data extraction and analysis, focusing on both technical (i.e., electrical protocol, type of electrode, plasmid) and medical (i.e., type of study, threated disease) aspects and highlighting the main differences in terms of results obtained. Moreover, the IGEA experience in the project “Transposon-based, targeted ex vivo gene therapy to treat age-related macular degeneration” (TargetAMD) was reported in the results section. No clinical trial was found on international literature and on ClinicalTrials.gov. Twelve preclinical studies were found including in vivo and ex-vivo applications. The studied showed that electrotransfer could be very efficient for plasmid DNA transfection. Many attempts such as modification of the electric field, buffers and electrodes have been made and the optimization of electric field setting seems to be very important. Using this technique, gene replacement can be designed in cases of retinal inheritance or corneal disease and a wide range of human eye diseases could, in the future, benefitfrom these gene therapy technologies.
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spelling doaj.art-816b4ffe25a64e9bba59b943c0a8e55b2023-12-01T23:27:40ZengMDPI AGBiomedicines2227-90592022-08-01108188910.3390/biomedicines10081889In Vivo and Ex Vivo Gene Electrotransfer in Ophthalmological DisordersRoberta Fusco0Giacomo Perazzolo Gallo1Elio Di Bernardo2Valeria D’Alessio3Mattia Ronchetti4Matteo Cadossi5Ruggero Cadossi6Oncology Medical and Research & Development Division, IGEA SpA, 41012 Carpi, ItalyOncology Medical and Research & Development Division, IGEA SpA, 41012 Carpi, ItalyOncology Medical and Research & Development Division, IGEA SpA, 41012 Carpi, ItalyOncology Medical and Research & Development Division, IGEA SpA, 41012 Carpi, ItalyRegulatory Affairs, BVI—Optikon 2000, 00138 Rome, ItalyOncology Medical and Research & Development Division, IGEA SpA, 41012 Carpi, ItalyOncology Medical and Research & Development Division, IGEA SpA, 41012 Carpi, ItalyThe aim of this document is to present an overview of gene electrotransfer in ophthalmological disorders. In order to ensure an adequate variety of the assessed studies, several electronic databases were considered and studies published between January 1998 and December 2021 were analysed. Three investigators carried out data extraction and analysis, focusing on both technical (i.e., electrical protocol, type of electrode, plasmid) and medical (i.e., type of study, threated disease) aspects and highlighting the main differences in terms of results obtained. Moreover, the IGEA experience in the project “Transposon-based, targeted ex vivo gene therapy to treat age-related macular degeneration” (TargetAMD) was reported in the results section. No clinical trial was found on international literature and on ClinicalTrials.gov. Twelve preclinical studies were found including in vivo and ex-vivo applications. The studied showed that electrotransfer could be very efficient for plasmid DNA transfection. Many attempts such as modification of the electric field, buffers and electrodes have been made and the optimization of electric field setting seems to be very important. Using this technique, gene replacement can be designed in cases of retinal inheritance or corneal disease and a wide range of human eye diseases could, in the future, benefitfrom these gene therapy technologies.https://www.mdpi.com/2227-9059/10/8/1889gene electrotransferophthalmological disordersin vivoex-vivo
spellingShingle Roberta Fusco
Giacomo Perazzolo Gallo
Elio Di Bernardo
Valeria D’Alessio
Mattia Ronchetti
Matteo Cadossi
Ruggero Cadossi
In Vivo and Ex Vivo Gene Electrotransfer in Ophthalmological Disorders
Biomedicines
gene electrotransfer
ophthalmological disorders
in vivo
ex-vivo
title In Vivo and Ex Vivo Gene Electrotransfer in Ophthalmological Disorders
title_full In Vivo and Ex Vivo Gene Electrotransfer in Ophthalmological Disorders
title_fullStr In Vivo and Ex Vivo Gene Electrotransfer in Ophthalmological Disorders
title_full_unstemmed In Vivo and Ex Vivo Gene Electrotransfer in Ophthalmological Disorders
title_short In Vivo and Ex Vivo Gene Electrotransfer in Ophthalmological Disorders
title_sort in vivo and ex vivo gene electrotransfer in ophthalmological disorders
topic gene electrotransfer
ophthalmological disorders
in vivo
ex-vivo
url https://www.mdpi.com/2227-9059/10/8/1889
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