Literature DB >> 22408006

Tyrosine-mutant AAV8 delivery of human MERTK provides long-term retinal preservation in RCS rats.

Wen-Tao Deng1, Astra Dinculescu, Qiuhong Li, Sanford L Boye, Jie Li, Marina S Gorbatyuk, Jijing Pang, Vince A Chiodo, Michael T Matthes, Douglas Yasumura, Li Liu, Fowzan S Alkuraya, Kang Zhang, Douglas Vollrath, Matthew M LaVail, William W Hauswirth.   

Abstract

PURPOSE: The absence of Mertk in RCS rats results in defective RPE phagocytosis, accumulation of outer segment (OS) debris in the subretinal space, and subsequent death of photoreceptors. Previous research utilizing Mertk gene replacement therapy in RCS rats provided proof of concept for treatment of this form of recessive retinitis pigmentosa (RP); however, the beneficial effects on retinal function were transient. In the present study, we evaluated whether delivery of a MERTK transgene using a tyrosine-mutant AAV8 capsid could lead to more robust and longer-term therapeutic outcomes than previously reported.
METHODS: An AAV8 Y733F vector expressing a human MERTK cDNA driven by a RPE-selective promoter was administrated subretinally at postnatal day 2. Functional and morphological analyses were performed at 4 months and 8 months post-treatment. Retinal vasculature and Müller cell activation were analyzed by quantifying acellular capillaries and glial fibrillary acidic protein immunostaining, respectively.
RESULTS: Electroretinographic responses from treated eyes were more than one-third of wild-type levels and OS were well preserved in the injection area even at 8 months. Rescue of RPE phagocytosis, prevention of retinal vasculature degeneration, and inhibition of Müller cell activation were demonstrated in the treated eyes for at least 8 months.
CONCLUSIONS: This research describes a longer and much more robust functional and morphological rescue than previous studies. We also demonstrate for the first time that an AAV8 mutant capsid serotype vector has a substantial therapeutic potential for RPE-specific gene delivery. These results suggest that tyrosine-mutant AAV8 vectors hold promise for the treatment of individuals with MERTK-associated RP.

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Year:  2012        PMID: 22408006      PMCID: PMC3995567          DOI: 10.1167/iovs.11-8831

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  45 in total

Review 1.  Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns.

Authors:  Carlo Rivolta; Dror Sharon; Margaret M DeAngelis; Thaddeus P Dryja
Journal:  Hum Mol Genet       Date:  2002-05-15       Impact factor: 6.150

2.  Subretinal injections in rodent eyes: effects on electrophysiology and histology of rat retina.

Authors:  A M Timmers; H Zhang; A Squitieri; C Gonzalez-Pola
Journal:  Mol Vis       Date:  2001-06-22       Impact factor: 2.367

3.  Retinal dystrophy in the rat--a pigment epithelial disease.

Authors:  W L Herron; B W Riegel; O E Myers; M L Rubin
Journal:  Invest Ophthalmol       Date:  1969-12

4.  Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively.

Authors:  Debra A Thompson; Christina L McHenry; Yun Li; Julia E Richards; Mohammad I Othman; Eberhard Schwinger; Douglas Vollrath; Samuel G Jacobson; Andreas Gal
Journal:  Am J Hum Genet       Date:  2001-11-27       Impact factor: 11.025

5.  Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk.

Authors:  D Vollrath; W Feng; J L Duncan; D Yasumura; P M D'Cruz; A Chappelow; M T Matthes; M A Kay; M M LaVail
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-09       Impact factor: 11.205

6.  Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat.

Authors:  P M D'Cruz; D Yasumura; J Weir; M T Matthes; H Abderrahim; M M LaVail; D Vollrath
Journal:  Hum Mol Genet       Date:  2000-03-01       Impact factor: 6.150

7.  AAV-Mediated gene transfer slows photoreceptor loss in the RCS rat model of retinitis pigmentosa.

Authors:  Alexander J Smith; Frank C Schlichtenbrede; Marion Tschernutter; James W Bainbridge; Adrian J Thrasher; Robin R Ali
Journal:  Mol Ther       Date:  2003-08       Impact factor: 11.454

8.  A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases.

Authors:  Elsebet Ostergaard; Morten Duno; Mustafa Batbayli; Kaj Vilhelmsen; Thomas Rosenberg
Journal:  Mol Vis       Date:  2011-06-04       Impact factor: 2.367

9.  Photoreceptor-pigment epithelial cell relationships in rats with inherited retinal degeneration. Radioautographic and electron microscope evidence for a dual source of extra lamellar material.

Authors:  M M LaVail; R L Sidman; D O'Neil
Journal:  J Cell Biol       Date:  1972-04       Impact factor: 10.539

10.  The role of the pigment epithelium in the etiology of inherited retinal dystrophy in the rat.

Authors:  D Bok; M O Hall
Journal:  J Cell Biol       Date:  1971-06       Impact factor: 10.539

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  35 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.  Gene Therapy for MERTK-Associated Retinal Degenerations.

Authors:  Matthew M LaVail; Douglas Yasumura; Michael T Matthes; Haidong Yang; William W Hauswirth; Wen-Tao Deng; Douglas Vollrath
Journal:  Adv Exp Med Biol       Date:  2016       Impact factor: 2.622

Review 3.  [Gene therapy as a treatment concept for inherited retinal diseases].

Authors:  J-S Bellingrath; M D Fischer
Journal:  Ophthalmologe       Date:  2015-09       Impact factor: 1.059

Review 4.  Gene therapy and genome surgery in the retina.

Authors:  James E DiCarlo; Vinit B Mahajan; Stephen H Tsang
Journal:  J Clin Invest       Date:  2018-06-01       Impact factor: 14.808

Review 5.  A comprehensive review of retinal gene therapy.

Authors:  Shannon E Boye; Sanford L Boye; Alfred S Lewin; William W Hauswirth
Journal:  Mol Ther       Date:  2013-01-29       Impact factor: 11.454

6.  Retinal gene therapy using adeno-associated viral vectors: multiple applications for a small virus.

Authors:  William W Hauswirth
Journal:  Hum Gene Ther       Date:  2014-08       Impact factor: 5.695

7.  Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration.

Authors:  Matthew M LaVail; Shimpei Nishikawa; Roy H Steinberg; Muna I Naash; Jacque L Duncan; Nikolaus Trautmann; Michael T Matthes; Douglas Yasumura; Cathy Lau-Villacorta; Jeannie Chen; Ward M Peterson; Haidong Yang; John G Flannery
Journal:  Exp Eye Res       Date:  2017-11-06       Impact factor: 3.467

Review 8.  CLINICAL PROGRESS IN INHERITED RETINAL DEGENERATIONS: GENE THERAPY CLINICAL TRIALS AND ADVANCES IN GENETIC SEQUENCING.

Authors:  Brian P Hafler
Journal:  Retina       Date:  2017-03       Impact factor: 4.256

9.  Targeted modifications in adeno-associated virus serotype 8 capsid improves its hepatic gene transfer efficiency in vivo.

Authors:  Dwaipayan Sen; Rupali A Gadkari; Govindarajan Sudha; Nishanth Gabriel; Yesupatham Sathish Kumar; Ruchita Selot; Rekha Samuel; Sumathi Rajalingam; V Ramya; Sukesh C Nair; Narayanaswamy Srinivasan; Alok Srivastava; Giridhara R Jayandharan
Journal:  Hum Gene Ther Methods       Date:  2013-04       Impact factor: 2.396

10.  Cone phosphodiesterase-6α' restores rod function and confers distinct physiological properties in the rod phosphodiesterase-6β-deficient rd10 mouse.

Authors:  Wen-Tao Deng; Keisuke Sakurai; Saravanan Kolandaivelu; Alexander V Kolesnikov; Astra Dinculescu; Jie Li; Ping Zhu; Xuan Liu; Jijing Pang; Vince A Chiodo; Sanford L Boye; Bo Chang; Visvanathan Ramamurthy; Vladimir J Kefalov; William W Hauswirth
Journal:  J Neurosci       Date:  2013-07-17       Impact factor: 6.167

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