RNA-based therapies in inherited retinal diseases

被引:25
作者
Girach, Aniz [1 ]
Audo, Isabelle [2 ,3 ,4 ,5 ]
Birch, David G. [6 ]
Huckfeldt, Rachel M. [7 ]
Lam, Byron L. [8 ]
Leroy, Bart P. [9 ,10 ,11 ,12 ,13 ]
Michaelides, Michel [14 ,15 ]
Russell, Stephen R. [16 ]
Sallum, Juliana M. F. [17 ,18 ]
Stingl, Katarina [19 ,20 ]
Tsang, Stephen H. [21 ,22 ,23 ]
Yang, Paul [24 ]
机构
[1] ProQR Therapeut, Zernikedreef 9, NL-2333 CK Leiden, Netherlands
[2] CHNO Quinze Vingts, Ctr Reference Malad Rares REFERET, Ctr Hosp Natl Ophtalmol Quinze Vingts, Paris, France
[3] CHNO Quinze Vingts, INSERM DHOS CIC 1423, Paris, France
[4] UCL, Inst Ophthalmol, London, England
[5] Sorbonne Univ, Inst Vis, CNRS, INSERM, Paris, France
[6] Retina Fdn Southwest, Dallas, TX USA
[7] Harvard Med Sch, Massachusetts Eye & Ear Infirm, Dept Ophthalmol, Boston, MA USA
[8] Univ Miami, Bascom Palmer Eye Inst, Miller Sch Med, Miami, FL USA
[9] Ghent Univ Hosp, Dept Ophthalmol, Ghent, Belgium
[10] Ghent Univ Hosp, Ctr Med Genet, Ghent, Belgium
[11] Univ Ghent, Ghent, Belgium
[12] Childrens Hosp Philadelphia, Div Ophthalmol, Philadelphia, PA USA
[13] Childrens Hosp Philadelphia, Ctr Cellular & Mol Therapeut, Philadelphia, PA USA
[14] UCL, UCL Inst Ophthalmol, London, England
[15] Moorfields Eye Hosp, London, England
[16] Univ Iowa, Inst Vis Res, Iowa City, IA USA
[17] Univ Fed Sao Paulo, Dept Ophthalmol, Sao Paulo, Brazil
[18] Inst Genet Ocular, Sao Paulo, Brazil
[19] Univ Tubingen, Univ Eye Hosp, Ctr Ophthalmol, Tubingen, Germany
[20] Univ Tubingen, Ctr Rare Eye Dis, Tubingen, Germany
[21] Columbia Univ, Vagelos Coll Phys & Surg, Jonas Childrens Vis Care, Columbia Stem Cell Initiat, New York, NY USA
[22] Columbia Univ, Vagelos Coll Phys & Surg, Shirlee Brown Glaucoma Lab, Columbia Stem Cell Initiat, New York, NY USA
[23] New York Presbyterian Hosp, Edward S Harkness Eye Inst, New York, NY USA
[24] Oregon Hlth & Sci Univ, Casey Eye Inst, Portland, OR USA
关键词
antisense oligonucleotides; genetic eye diseases; inherited retinal diseases; QR-1123; RNA therapies; sepofarsen; ultevursen; LEBER CONGENITAL AMAUROSIS; GENE-THERAPY; RETINITIS-PIGMENTOSA; IN-VITRO; CEP290; MUTATIONS; LCA; IMPROVEMENT; FEATURES; VISION;
D O I
10.1177/25158414221134602
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Inherited retinal diseases (IRDs) are a genetically and phenotypically heterogeneous group of genetic eye disorders. There are more than 300 disease entities, and together this group of disorders affects millions of people globally and is a frequent cause of blindness or low-vision certification. However, each type is rare or ultra-rare. Characteristically, the impaired vision in IRDs is due to retinal photoreceptor dysfunction and loss resulting from mutation in a gene that codes for a retinal protein. Historically, IRDs have been considered incurable and individuals living with these blinding conditions could be offered only supportive care. However, the treatment landscape for IRDs is beginning to evolve. Progress is being made, driven by improvements in understanding of genotype-phenotype relationships, through advances in molecular genetic testing and retinal imaging. Alongside this expanding knowledge of IRDs, the current era of precision medicine is fueling a growth in targeted therapies. This has resulted in the first treatment for an IRD being approved. Several other therapies are currently in development in the IRD space, including RNA-based therapies, gene-based therapies (such as augmentation therapy and gene editing), cell therapy, visual prosthetics, and optogenetics. RNA-based therapies are a novel approach within precision medicine that have demonstrated success, particularly in rare diseases. Three antisense oligonucleotides (AONs) are currently in development for the treatment of specific IRD subtypes. These RNA-based therapies bring several key advantages in the setting of IRDs, and the potential to bring meaningful vision benefit to individuals living with inherited blinding disorders. This review will examine the increasing breadth and relevance of RNA-based therapies in clinical medicine, explore the key features that make AONs suitable for treating genetic eye diseases, and provide an overview of the three-leading investigational AONs in clinical trials.
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