Evidence map›Paper›PMID 27664291›Full record

ReviewOphthalmology2016

Gene Therapy and Stem Cell Transplantation in Retinal Disease: The New Frontier.

Robert E MacLaren, Jean Bennett, Steven D Schwartz

Open access · greenAbstract readReview
In one paragraph

Review in Ophthalmology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.6field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Monitoring Gene Expression in Retina with synthetic serum markers.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Stem cell therapy in retinal diseases.Neural regeneration research · 2023
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Retina stem cells, hopes and obstacles.World journal of stem cells · 2021
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 2 countries.

Robert E MacLarenNuffield Laboratory of Ophthalmology, Department of Clinical Neurosciences, University of Oxford and Oxford University Eye Hospital, NHS Foundation Trust, NIHR Biomedical Research Centre, Oxford, United Kingdom; Moorfields Eye Hospital, NHS Foundation Trust, NIHR Biomedical Research Centre, London, United Kingdom. Electronic address: enquiries@eye.ox.ac.uk.
Jean BennettCenter for Advanced Retinal and Ocular Therapeutics, Department of Ophthalmology, The Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
Steven D SchwartzRetina Division, Department of Ophthalmology, Stein Eye Institute, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California.
Children's Hospital of Philadelphia · USMoorfields Eye Hospital NHS Foundation Trust · GBUniversity of California, Los Angeles · US

Funding

Therapeutic approaches for ABCA4-associated disordersR24EY019861 · NEI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ALLIKMETS, RANDO L · 2011 to 2015
$7.2M
Broad Spectrum Molecular Therapy for Blinding Retina DisordersDP1EY023177 · NEI · UNIVERSITY OF PENNSYLVANIA · PI BENNETT, JEAN · 2012 to 2015
$3.2M
Plasticity of the human visual system studied in response to retinal gene therapyR01EY025287 · NEI · UNIVERSITY OF PENNSYLVANIA · PI ASHTARI, MANZAR · 2016 to 2020
$2.4M
Longitudinal Neuroimaging of Leber's Congenital Amaurosis After Gene TherapyR21EY020662 · NEI · CHILDREN'S HOSP OF PHILADELPHIA · PI ASHTARI, MANZAR · 2011 to 2012
$440k
An Inducible System for Gene DeliveryR21EB018064 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI BENNETT, JEAN, LEWIS, MITCHELL · 2015 to 2016
$430k
NEI NIH HHS DP1 EY023177NEI NIH HHS R01 EY025287NEI NIH HHS R21 EY020662NEI NIH HHS R24 EY019861NIBIB NIH HHS R21 EB018064Wellcome Trust
6 · The paper itself

Abstract

Gene and cell therapies have the potential to prevent, halt, or reverse diseases of the retina in patients with currently incurable blinding conditions. Over the past 2 decades, major advances in our understanding of the pathobiologic basis of retinal diseases, coupled with growth of gene transfer and cell transplantation biotechnologies, have created optimism that previously blinding retinal conditions may be treatable. It is now possible to deliver cloned genes safely and stably to specific retinal cell types in humans. Preliminary results testing gene augmentation strategies in human recessive diseases suggest promising safety and efficacy profiles, including improved visual function outcomes over extended periods. Additional gene-based strategies under development include approaches to autosomal dominant disease ("gain of function"), attempts to deliver genes encoding therapeutic proteins with proven mechanisms of action interfering with specific disease pathways, and approaches that could be used to render retinal cells other than atrophied photoreceptors light sensitive. In the programs that are the furthest along-pivotal regulatory safety and efficacy trials studying individuals with retinal degeneration resulting from RPE65 mutations-initial results reveal a robust safety profile and clinically significant improvements in visual function, thereby making this program a frontrunner for the first approved gene therapy product in the United States. Similar to gene therapy, progress in regenerative or stem cell-based transplantation strategies has been substantial. It is now possible to deliver safely stem cell-derived, terminally differentiated, biologically and genetically defined retinal pigment epithelium (RPE) to the diseased human eye. Although demonstration of clinical efficacy is still well behind the gene therapy field, multiple programs investigating regenerative strategies in RPE disease are beginning to enroll subjects, and initial results suggest possible signs of efficacy. Stem cells capable of becoming other retinal cell types, such as photoreceptors, are on the cusp of clinical trials. Stem cell-derived transplants can be delivered to precise target locations in the eye, and their ability to ameliorate, reverse, regenerate, or neuroprotect against disease processes can be assessed. Results from these studies will provide foundational knowledge that may lead to clinically significant therapies for currently untreatable retinal disease.

Indexed as

DependovirusEmbryonic Stem CellsGenetic TherapyHumansPluripotent Stem CellsRegenerative MedicineRetinal DiseasesRetinal Pigment EpitheliumStem Cell TransplantationTransplantation Immunology

Identifiers

PMID27664291
PMCPMC5545086
OpenAlexW2522284209

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.