Evidence map›Paper›PMID 35102278›Full record

ReviewNature biomedical engineering2023

Bioengineering strategies for restoring vision.

Jasmina Cehajic-Kapetanovic, Mandeep S Singh, Eberhart Zrenner, Robert E MacLaren

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature biomedical engineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.3field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 76 citations in OpenAlex.

  1. Microfluidic platform for nanoliter qPCR of several retinal pigment epithelial (RPE) cells.Journal of micromechanics and microengineering : structures, devices, and systems · 2026
    Article
  2. Article
  3. Article
  4. Neural Vision Restoration in Ophthalmology.Annals of biomedical engineering · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Future Frontiers in Bioinspired Implanted Biomaterials.Advanced materials (Deerfield Beach, Fla.) · 2025
    Review
  11. Article
  12. A synthetic opsin restores vision in patients with severe retinal degeneration.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  13. Perspectives and open questions in vision restoration with vMCO-010.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  14. Rekindling Vision: Innovative Strategies for Treating Retinal Degeneration.International journal of molecular sciences · 2025
    Review
  15. Article
  16. Robotising vitreoretinal surgeries.Eye (London, England) · 2025
    Review
  17. Review
  18. Article
  19. Article
  20. Article
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

4 authors at 3 institutions in 2 countries.

Jasmina Cehajic-KapetanovicNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, UK. enquiries@ndcn.ox.ac.uk.ORCID 0000-0002-9956-6412
Mandeep S SinghJohns Hopkins Medical Institute, Baltimore, MD, USA.
Eberhart ZrennerInstitute for Ophthalmic Research, Center for Ophthalmology, University of Tübingen, Tübingen, Germany.ORCID 0000-0003-2846-9663
Robert E MacLarenNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, UK.ORCID 0000-0002-3096-4682
Nuffield Orthopaedic Centre · GBSTZ eyetrial · DEUniversity of Oxford · GB

Funding

Developing photoreceptor repair for macular degeneration therapy.R01EY033103 · NEI · JOHNS HOPKINS UNIVERSITY · PI SINGH, MANDEEP · 2021 to 2025
$2.0M
Department of HealthMedical Research Council MR/V029762/1NEI NIH HHS R01 EY033103
6 · The paper itself

Abstract

Late-stage retinal degenerative disease involving photoreceptor loss can be treated by optogenetic therapy, cell transplantation and retinal prostheses. These approaches aim to restore light sensitivity to the retina as well as visual perception by integrating neuronal responses for transmission to the cortex. In age-related macular degeneration, some cell-based therapies also aim to restore photoreceptor-supporting tissue to prevent complete photoreceptor loss. In the earlier stages of degeneration, gene-replacement therapy could attenuate retinal-disease progression and reverse loss of function. And gene-editing strategies aim to correct the underlying genetic defects. In this Review, we highlight the most promising gene therapies, cell therapies and retinal prostheses for the treatment of retinal disease, discuss the benefits and drawbacks of each treatment strategy and the factors influencing whether functional tissue is reconstructed and repaired or replaced with an electronic device, and summarize upcoming technologies for enhancing the restoration of vision.

Indexed as

RetinaRetinal DegenerationBioengineeringCell TransplantationHumansVision, Ocular

Identifiers

PMID35102278
OpenAlexW4210615010

What OpenQuestion holds

Textmetadata
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.