Evidence map›Paper›PMID 39171529›Full record

ArticleJCI insight2024

Evaluating precision medicine approaches for gene therapy in patient-specific cellular models of Bietti crystalline dystrophy.

Yao Li, Richard R Yang, Yong-Shi Li, Chun-Wei Hsu, Laura A Jenny, Yang Kong, Merry Zc Ruan, Janet R Sparrow, Stephen H Tsang

Abstract read
In one paragraph

Article in JCI insight, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Hereditary spastic paraplegia: from decades of therapy to future innovations.Therapeutic advances in neurological disorders · 2026
    Review
  3. Article
  4. Article
  5. Observational
  6. 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

9 authors.

Yao LiJonas Children's Vision Care, Department of Ophthalmology, Columbia University, New York, New York, USA.
Richard R YangReflection Biotechnologies, New Territories, Hong Kong.
Yong-Shi LiJonas Children's Vision Care, Department of Ophthalmology, Columbia University, New York, New York, USA.
Chun-Wei HsuJonas Children's Vision Care, Department of Ophthalmology, Columbia University, New York, New York, USA.
Laura A JennyJonas Children's Vision Care, Department of Ophthalmology, Columbia University, New York, New York, USA.
Yang KongJonas Children's Vision Care, Department of Ophthalmology, Columbia University, New York, New York, USA.
Merry Zc RuanVagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA.
Janet R SparrowDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.
Stephen H TsangJonas Children's Vision Care, Department of Ophthalmology, Columbia University, New York, New York, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patient-specific induced pluripotent stem cell-derived (iPSC-derived) cell lines allow for therapies to be tailored to individual patients, increasing therapeutic precision and efficiency. Bietti crystalline dystrophy (BCD) is a rare blinding disease estimated to affect about 67,000 individuals worldwide. Here, we used iPSC-derived retinal pigment epithelium (iRPE) cells from patients with BCD to evaluate adeno-associated virus-mediated (AAV-mediated) gene augmentation therapy strategies. We found that BCD iRPE cells were vulnerable to blue light-induced oxidative stress and that cellular phenotype can be quantified using 3 robust biomarkers: reactive oxygen species (ROS), 4-hydroxy 2-nonenal (4-HNE) levels, and cell death rate. Additionally, we demonstrated that AAV-mediated gene therapy can significantly reduce light-induced cell death in BCD iRPE cells. This is the first proof-of-concept study to our knowledge to show that AAV-CYP4V2 gene therapy can be used to treat light-induced RPE damage in BCD. Furthermore, we observed significant variability in cellular phenotypes among iRPE from patients with BCD of divergent mutations, which outlined genotype-phenotype correlations in BCD patient-specific cell disease models. Our results reveal that patient-specific iRPE cells retained personalized responses to AAV-mediated gene therapy. Therefore, this approach can advance BCD therapy and set a precedent for precision medicine in other diseases, emphasizing the necessity for personalization in healthcare to accommodate individual diversity.

Indexed as

Corneal Dystrophies, HereditaryDependovirusGenetic TherapyInduced Pluripotent Stem CellsPrecision MedicineRetinal Pigment EpitheliumAldehydesCytochrome P450 Family 4HumansMaleOxidative StressReactive Oxygen SpeciesRetinal Diseases4-hydroxy-2-nonenalAldehydesCYP4V2 protein, humanCytochrome P450 Family 4Reactive Oxygen SpeciesGene therapyGenetic diseasesiPS cellsOphthalmologyTherapeutics

Identifiers

PMID39171529
PMCPMC11343589

What Socratic holds

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LicenceCC BY
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.