Literature DB >> 32568387

Limited time window for retinal gene therapy in a preclinical model of ciliopathy.

Poppy Datta1,2, Avri Ruffcorn1,2, Seongjin Seo1,2.   

Abstract

Retinal degeneration is a common clinical feature of ciliopathies, a group of genetic diseases linked to ciliary dysfunction, and gene therapy is an attractive treatment option to prevent vision loss. Although the efficacy of retinal gene therapy is well established by multiple proof-of-concept preclinical studies, its long-term effect, particularly when treatments are given at advanced disease stages, is controversial. Incomplete treatment and intrinsic variability of gene delivery methods may contribute to the variable outcomes. Here, we used a genetic rescue approach to 'optimally' treat retinal degeneration at various disease stages and examined the long-term efficacy of gene therapy in a mouse model of ciliopathy. We used a Bardet-Biedl syndrome type 17 (BBS17) mouse model, in which the gene-trap that suppresses Bbs17 (also known as Lztfl1) expression can be removed by tamoxifen administration, restoring normal gene expression systemically. Our data indicate that therapeutic effects of retinal gene therapy decrease gradually as treatments are given at later stages. These results suggest the presence of limited time window for successful gene therapy in certain retinal degenerations. Our study also implies that the long-term efficacy of retinal gene therapy may depend on not only the timing of treatment but also other factors such as the function of mutated genes and residual activities of mutant alleles.
© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Year:  2020        PMID: 32568387      PMCID: PMC7424757          DOI: 10.1093/hmg/ddaa124

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  70 in total

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Journal:  Development       Date:  2006-12-13       Impact factor: 6.868

2.  Intraflagellar transport proteins in ciliogenesis of photoreceptor cells.

Authors:  Tina Sedmak; Uwe Wolfrum
Journal:  Biol Cell       Date:  2011-10-01       Impact factor: 4.458

Review 3.  Photoreceptor Cilia and Retinal Ciliopathies.

Authors:  Kinga M Bujakowska; Qin Liu; Eric A Pierce
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-10-03       Impact factor: 10.005

4.  Retinal gene therapy coming of age.

Authors:  Connie L Cepko; Luk H Vandenberghe
Journal:  Hum Gene Ther       Date:  2013-03       Impact factor: 5.695

5.  Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes.

Authors:  Qihong Zhang; Darryl Nishimura; Seongjin Seo; Tim Vogel; Donald A Morgan; Charles Searby; Kevin Bugge; Edwin M Stone; Kamal Rahmouni; Val C Sheffield
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-02       Impact factor: 11.205

6.  Genetic rescue models refute nonautonomous rod cell death in retinitis pigmentosa.

Authors:  Susanne F Koch; Jimmy K Duong; Chun-Wei Hsu; Yi-Ting Tsai; Chyuan-Sheng Lin; Christian A Wahl-Schott; Stephen H Tsang
Journal:  Proc Natl Acad Sci U S A       Date:  2017-05-03       Impact factor: 11.205

7.  The retina of the newborn human infant.

Authors:  I Abramov; J Gordon; A Hendrickson; L Hainline; V Dobson; E LaBossiere
Journal:  Science       Date:  1982-07-16       Impact factor: 47.728

8.  Accumulation of non-outer segment proteins in the outer segment underlies photoreceptor degeneration in Bardet-Biedl syndrome.

Authors:  Poppy Datta; Chantal Allamargot; Joseph S Hudson; Emily K Andersen; Sajag Bhattarai; Arlene V Drack; Val C Sheffield; Seongjin Seo
Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-27       Impact factor: 11.205

9.  Mesoaxial polydactyly is a major feature in Bardet-Biedl syndrome patients with LZTFL1 (BBS17) mutations.

Authors:  E Schaefer; J Lauer; M Durand; V Pelletier; C Obringer; A Claussmann; J-J Braun; C Redin; C Mathis; J Muller; C Schmidt-Mutter; E Flori; V Marion; C Stoetzel; H Dollfus
Journal:  Clin Genet       Date:  2013-06-12       Impact factor: 4.438

10.  Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial.

Authors:  William W Hauswirth; Tomas S Aleman; Shalesh Kaushal; Artur V Cideciyan; Sharon B Schwartz; Lili Wang; Thomas J Conlon; Sanford L Boye; Terence R Flotte; Barry J Byrne; Samuel G Jacobson
Journal:  Hum Gene Ther       Date:  2008-10       Impact factor: 5.695

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  4 in total

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Authors:  Poppy Datta; J Thomas Cribbs; Seongjin Seo
Journal:  PLoS One       Date:  2021-05-07       Impact factor: 3.240

2.  Current and Future Treatment of Retinitis Pigmentosa.

Authors:  Nancy Cross; Cécile van Steen; Yasmina Zegaoui; Andrew Satherley; Luigi Angelillo
Journal:  Clin Ophthalmol       Date:  2022-08-31

3.  Progressive retinal degeneration of rods and cones in a Bardet-Biedl syndrome type 10 mouse model.

Authors:  Sara K Mayer; Jacintha Thomas; Megan Helms; Aishwarya Kothapalli; Ioana Cherascu; Adisa Salesevic; Elliot Stalter; Kai Wang; Poppy Datta; Charles Searby; Seongjin Seo; Ying Hsu; Sajag Bhattarai; Val C Sheffield; Arlene V Drack
Journal:  Dis Model Mech       Date:  2022-09-20       Impact factor: 5.732

4.  Bardet-Biedl syndrome-7 (BBS7) shows treatment potential and a cone-rod dystrophy phenotype that recapitulates the non-human primate model.

Authors:  Tomas S Aleman; Erin C O'Neil; Keli O'Connor; Yu You Jiang; Isabella A Aleman; Jean Bennett; Jessica I W Morgan; Brian W Toussaint
Journal:  Ophthalmic Genet       Date:  2021-03-17       Impact factor: 1.274

  4 in total

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