Ocular gene therapy for choroideremia: clinical trials and future perspectives

<strong>Introduction:</strong> Gene therapy offers the potential for targeted replacement of single gene defects in inherited retinal degenerations. <strong>Areas covered:</strong> Choroideremia is an X-linked blinding retinal disease resulting from deficiency of the CHM gen...

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Main Authors: Xue, K, Maclaren, R
Format: Journal article
Published: Taylor and Francis 2018
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author Xue, K
Maclaren, R
author_facet Xue, K
Maclaren, R
author_sort Xue, K
collection OXFORD
description <strong>Introduction:</strong> Gene therapy offers the potential for targeted replacement of single gene defects in inherited retinal degenerations. <strong>Areas covered:</strong> Choroideremia is an X-linked blinding retinal disease resulting from deficiency of the CHM gene product, REP1. The disease represents an ideal target for retinal gene therapy, as it is readily diagnosed in the clinic, relatively homogenous in phenotype and slow progressing, thereby providing a wide therapeutic window for intervention. Ongoing clinical trials of retinal gene therapy for choroideremia using an adeno-associated viral vector have demonstrated safety and early efficacy. We review the clinical characteristics of the disease with a view to interpreting the findings of gene therapy clinical trials and discuss future directions. <strong>Expert commentary:</strong> Choroideremia gene therapy has so far demonstrated good safety profile and early functional visual acuity gains in a proportion of trial participants, which appear to be sustained.
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spelling oxford-uuid:b8ecd08b-1d80-45d2-9219-e419ae8cb1f92022-03-27T04:59:26ZOcular gene therapy for choroideremia: clinical trials and future perspectivesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b8ecd08b-1d80-45d2-9219-e419ae8cb1f9Symplectic Elements at OxfordTaylor and Francis2018Xue, KMaclaren, R<strong>Introduction:</strong> Gene therapy offers the potential for targeted replacement of single gene defects in inherited retinal degenerations. <strong>Areas covered:</strong> Choroideremia is an X-linked blinding retinal disease resulting from deficiency of the CHM gene product, REP1. The disease represents an ideal target for retinal gene therapy, as it is readily diagnosed in the clinic, relatively homogenous in phenotype and slow progressing, thereby providing a wide therapeutic window for intervention. Ongoing clinical trials of retinal gene therapy for choroideremia using an adeno-associated viral vector have demonstrated safety and early efficacy. We review the clinical characteristics of the disease with a view to interpreting the findings of gene therapy clinical trials and discuss future directions. <strong>Expert commentary:</strong> Choroideremia gene therapy has so far demonstrated good safety profile and early functional visual acuity gains in a proportion of trial participants, which appear to be sustained.
spellingShingle Xue, K
Maclaren, R
Ocular gene therapy for choroideremia: clinical trials and future perspectives
title Ocular gene therapy for choroideremia: clinical trials and future perspectives
title_full Ocular gene therapy for choroideremia: clinical trials and future perspectives
title_fullStr Ocular gene therapy for choroideremia: clinical trials and future perspectives
title_full_unstemmed Ocular gene therapy for choroideremia: clinical trials and future perspectives
title_short Ocular gene therapy for choroideremia: clinical trials and future perspectives
title_sort ocular gene therapy for choroideremia clinical trials and future perspectives
work_keys_str_mv AT xuek oculargenetherapyforchoroideremiaclinicaltrialsandfutureperspectives
AT maclarenr oculargenetherapyforchoroideremiaclinicaltrialsandfutureperspectives