Evidence map›Paper›PMID 36430270›Full record

ReviewInternational journal of molecular sciences2022

Pluripotent Stem Cells in Clinical Cell Transplantation: Focusing on Induced Pluripotent Stem Cell-Derived RPE Cell Therapy in Age-Related Macular Degeneration.

Yi-Ping Yang, Yu-Jer Hsiao, Kao-Jung Chang, Shania Foustine, Yu-Ling Ko, Yi-Ching Tsai, Hsiao-Yun Tai, Yu-Chieh Ko, Shih-Hwa Chiou, Tai-Chi Lin and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Yi-Ping YangDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
Yu-Jer HsiaoDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.ORCID 0000-0002-0783-605X
Kao-Jung ChangDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.ORCID 0000-0002-2238-7387
Shania FoustineInstitute of Pharmacology, College of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.
Yu-Ling KoDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
Yi-Ching TsaiDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
Hsiao-Yun TaiDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
Yu-Chieh KoDepartment of Ophthalmology, Taipei Veterans General Hospital, Taipei 112201, Taiwan.ORCID 0000-0002-0818-4962
Shih-Hwa ChiouDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
Tai-Chi LinSchool of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.
Shih-Jen ChenDepartment of Ophthalmology, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
Yueh ChienDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.ORCID 0000-0002-1528-9252
De-Kuang HwangSchool of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.ORCID 0000-0001-6346-8485
National Yang Ming Chiao Tung University · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human pluripotent stem cells (PSCs), including both embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs), represent valuable cell sources to replace diseased or injured tissues in regenerative medicine. iPSCs exhibit the potential for indefinite self-renewal and differentiation into various cell types and can be reprogrammed from somatic tissue that can be easily obtained, paving the way for cell therapy, regenerative medicine, and personalized medicine. Cell therapies using various iPSC-derived cell types are now evolving rapidly for the treatment of clinical diseases, including Parkinson's disease, hematological diseases, cardiomyopathy, osteoarthritis, and retinal diseases. Since the first interventional clinical trial with autologous iPSC-derived retinal pigment epithelial cells (RPEs) for the treatment of age-related macular degeneration (AMD) was accomplished in Japan, several preclinical trials using iPSC suspensions or monolayers have been launched, or are ongoing or completed. The evolution and generation of human leukocyte antigen (HLA)-universal iPSCs may facilitate the clinical application of iPSC-based therapies. Thus, iPSCs hold great promise in the treatment of multiple retinal diseases. The efficacy and adverse effects of iPSC-based retinal therapies should be carefully assessed in ongoing and further clinical trials.

Indexed as

Induced Pluripotent Stem CellsMacular DegenerationRetinal DiseasesCell- and Tissue-Based TherapyCell TransplantationHumansRetinal Pigment Epitheliumage-related macular degenerationcell transplantationclinical trialsembryonic stem cellsinduced pluripotent stem cellpluripotent stem cellsretinal pigment epithelial cells

Identifiers

PMID36430270
PMCPMC9696562
OpenAlexW4308872473

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.