Literature DB >> 19303164

Prospects for retinal gene replacement therapy.

Alexander J Smith1, James W Bainbridge, Robin R Ali.   

Abstract

Inherited retinal degeneration, which includes conditions such as retinitis pigmentosa and Leber congenital amaurosis (LCA), affects approximately 1/3000 of the population in the Western world. It is characterized by loss of vision and results from mutations in any one of >100 different genes. There are currently no effective treatments, but many of the genes have now been identified and their functions elucidated, providing a major impetus to develop gene-based treatments. Preliminary results from three clinical trials indicate that the treatment of a form of LCA by gene therapy can be safe and effective. Here, we discuss the potential for treating other forms of retinal degeneration by gene therapy, focusing on the gene defects that are likely to be the most amenable to treatment.

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Year:  2009        PMID: 19303164     DOI: 10.1016/j.tig.2009.02.003

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  34 in total

Review 1.  Synthetic biology with surgical precision: targeted reengineering of signaling proteins.

Authors:  Vsevolod V Gurevich; Eugenia V Gurevich
Journal:  Cell Signal       Date:  2012-06-01       Impact factor: 4.315

2.  Task-dependent V1 responses in human retinitis pigmentosa.

Authors:  Yoichiro Masuda; Hiroshi Horiguchi; Serge O Dumoulin; Ayumu Furuta; Satoru Miyauchi; Satoshi Nakadomari; Brian A Wandell
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-05-05       Impact factor: 4.799

Review 3.  Mitochondrial medicine: to a new era of gene therapy for mitochondrial DNA mutations.

Authors:  Hélène Cwerman-Thibault; José-Alain Sahel; Marisol Corral-Debrinski
Journal:  J Inherit Metab Dis       Date:  2010-06-23       Impact factor: 4.982

4.  Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic mice.

Authors:  Haoyu Mao; Marina S Gorbatyuk; Brian Rossmiller; William W Hauswirth; Alfred S Lewin
Journal:  Hum Gene Ther       Date:  2012-03-28       Impact factor: 5.695

Review 5.  Channelrhodopsins provide a breakthrough insight into strategies for curing blindness.

Authors:  Hiroshi Tomita; Eriko Sugano; Hitomi Isago; Makoto Tamai
Journal:  J Genet       Date:  2009-12       Impact factor: 1.166

6.  Implantation and explantation of an active epiretinal visual prosthesis: 2-year follow-up data from the EPIRET3 prospective clinical trial.

Authors:  J Menzel-Severing; T Laube; C Brockmann; N Bornfeld; W Mokwa; B Mazinani; P Walter; G Roessler
Journal:  Eye (Lond)       Date:  2012-03-16       Impact factor: 3.775

Review 7.  Gene therapy of inherited retinopathies: a long and successful road from viral vectors to patients.

Authors:  Pasqualina Colella; Alberto Auricchio
Journal:  Hum Gene Ther       Date:  2012-08       Impact factor: 5.695

Review 8.  X-linked juvenile retinoschisis: clinical diagnosis, genetic analysis, and molecular mechanisms.

Authors:  Robert S Molday; Ulrich Kellner; Bernhard H F Weber
Journal:  Prog Retin Eye Res       Date:  2012-01-03       Impact factor: 21.198

9.  Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization.

Authors:  Ning Zhang; Alexander V Kolesnikov; Beata Jastrzebska; Debarshi Mustafi; Osamu Sawada; Tadao Maeda; Christel Genoud; Andreas Engel; Vladimir J Kefalov; Krzysztof Palczewski
Journal:  J Clin Invest       Date:  2012-12-10       Impact factor: 14.808

10.  Retinitis pigmentosa and allied conditions today: a paradigm of translational research.

Authors:  Carmen Ayuso; Jose M Millan
Journal:  Genome Med       Date:  2010-05-27       Impact factor: 11.117

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