Evidence map›Paper›PMID 36041146›Full record

ReviewAsia-Pacific journal of ophthalmology (Philadelphia, Pa.)

The Prospects for Retinal Organoids in Treatment of Retinal Diseases.

Yuntian Xue, Bin Lin, Jacqueline T Chen, William C Tang, Andrew W Browne, Magdalene J Seiler

Abstract readReview
In one paragraph

Review in Asia-Pacific journal of ophthalmology (Philadelphia, Pa.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Monitoring Gene Expression in Retina with synthetic serum markers.bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Animal models for the evaluation of retinal stem cell therapies.Progress in retinal and eye research · 2025
    Review
  8. Article
  9. Retinal Organoids: Innovative Tools for Understanding Retinal Degeneration.International journal of molecular sciences · 2025
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. 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

6 authors.

Yuntian XueBiomedical Engineering, University of California, Irvine, CA.
Bin LinStem Cell Research Center, University of California, Irvine, CA.
Jacqueline T ChenStem Cell Research Center, University of California, Irvine, CA.
William C TangBiomedical Engineering, University of California, Irvine, CA.
Andrew W BrowneBiomedical Engineering, University of California, Irvine, CA.
Magdalene J SeilerStem Cell Research Center, University of California, Irvine, CA.

Funding

Institutional Career Development CoreKL2TR001416 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAIOZZO, VINCENT JAMES, DEMETRIOU, MICHAEL · 2015 to 2023
$5.6M
Integration and functionality of retinal organoid transplantsR01EY031834 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI SEILER, MAGDALENE J · 2021 to 2025
$3.0M
VRC: A Stem Cell-Based Treatment Strategy for Laser-Induced Permanent Retinal DamagesR01EY031144 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI THOMAS, BIJU BLAVADY · 2019 to 2021
$751k
NCATS NIH HHS KL2 TR001416NEI NIH HHS R01 EY031144NEI NIH HHS R01 EY031834
6 · The paper itself

Abstract

Retinal degeneration (RD) is a significant cause of incurable blindness worldwide. Photoreceptors and retinal pigmented epithelium are irreversibly damaged in advanced RD. Functional replacement of photoreceptors and/or retinal pigmented epithelium cells is a promising approach to restoring vision. This paper reviews the current status and explores future prospects of the transplantation therapy provided by pluripotent stem cell-derived retinal organoids (ROs). This review summarizes the status of rodent RD disease models and discusses RO culture and analytical tools to evaluate RO quality and function. Finally, we review and discuss the studies in which RO-derived cells or sheets were transplanted. In conclusion, methods to derive ROs from pluripotent stem cells have significantly improved and become more efficient in recent years. Meanwhile, more novel technologies are applied to characterize and validate RO quality. However, opportunity remains to optimize tissue differentiation protocols and achieve better RO reproducibility. In order to screen high-quality ROs for downstream applications, approaches such as noninvasive and label-free imaging and electrophysiological functional testing are promising and worth further investigation. Lastly, transplanted RO-derived tissues have allowed improvements in visual function in several RD models, showing promises for clinical applications in the future.

Indexed as

OrganoidsRetinal DegenerationHumansReactive Oxygen SpeciesReproducibility of ResultsRetinaReactive Oxygen Species

Identifiers

PMID36041146
PMCPMC9966053

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.