Evidence map›Paper›PMID 25984235›Full record

ArticleFibrogenesis & tissue repair2015

Prospects for clinical use of reprogrammed cells for autologous treatment of macular degeneration.

Ana Belen Alvarez Palomo, Samuel McLenachan, Fred K Chen, Lyndon Da Cruz, Rodney J Dilley, Jordi Requena, Michaela Lucas, Andrew Lucas, Micha Drukker, Michael J Edel

Open access · hybridAbstract read
In one paragraph

Article in Fibrogenesis & tissue repair, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 26 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

10 authors at 8 institutions in 4 countries.

Ana Belen Alvarez PalomoControl of Pluripotency Laboratory, Department of Physiological Sciences I, Faculty of Medicine, University of Barcelona, Hospital Clinic, Casanova 143, 08036 Barcelona, Spain.
Samuel McLenachanCentre for Ophthalmology and Visual Science (Lions Eye Institute), University of Western Australia, 2 Verdun Street, Nedlands, WA 6009 Australia.
Fred K ChenCentre for Ophthalmology and Visual Science (Lions Eye Institute), University of Western Australia, 2 Verdun Street, Nedlands, WA 6009 Australia.
Lyndon Da CruzMoorfields Eye Hospital, 162 City Road, London, EC1V 2PD England.
Rodney J DilleyEar Sciences Centre, 1 Salvado Rd, Subiaco, WA 6008 Australia ; School of Surgery, University of Western Australia, 35 Stirling Highway, Nedlands, WA 6009 Australia.
Jordi RequenaControl of Pluripotency Laboratory, Department of Physiological Sciences I, Faculty of Medicine, University of Barcelona, Hospital Clinic, Casanova 143, 08036 Barcelona, Spain.
Michaela LucasSchool of Medicine and Pharmacology, University of Western Australia, 35 Stirling Highway, Nedlands, WA 6009 Australia ; PathWest, SCGH Laboratories Hospital Ave, Nedlands, WA 6009 Australia.
Andrew LucasInstitute for Immunology and Infectious Diseases, Murdoch University, Building 390, Discovery Way, Murdoch, Perth, WA 6150 Australia.
Micha DrukkerHelmholtz Zentrum München, German Research Centre for Environmental Health (GmbH), Institute of Stem Cell Research, Ingolstädter Landstraße 1, D-85764 Neuherberg, Germany.
Michael J EdelControl of Pluripotency Laboratory, Department of Physiological Sciences I, Faculty of Medicine, University of Barcelona, Hospital Clinic, Casanova 143, 08036 Barcelona, Spain ; Division of Pediatrics and Child Health, Westmead Children's Hospital, Corner Hawkesbury Road and Hainsworth Street, Westmead, Sydney, NSW 2145 Australia ; School of Anatomy, Physiology & Human Biology and Centre for Cell Therapy and Regenerative Medicine (CCTRM), University of Western Australia, 35 Stirling Highway, Nedlands, WA 6009 Australia.
Universitat de Barcelona · ESUniversity of Western Australia · AUChildren's Hospital at Westmead · AUEar Science Institute Australia · AUHelmholtz Zentrum München · DELions Eye Institute · AUMoorfields Eye Hospital NHS Foundation Trust · GBMurdoch University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the discovery of induced pluripotent stem cells (iPSC) in 2006, the symptoms of many human diseases have been reversed in animal models with iPSC therapy, setting the stage for future clinical development. From the animal data it is clear that iPSC are rapidly becoming the lead cell type for cell replacement therapy and for the newly developing field of iPSC-derived body organ transplantation. The first human pathology that might be treated in the near future with iPSC is age-related macular degeneration (AMD), which has recently passed the criteria set down by regulators for phase I clinical trials with allogeneic human embryonic stem cell-derived cell transplantation in humans. Given that iPSC are currently in clinical trial in Japan (RIKEN) to treat AMD, the establishment of a set of international criteria to make clinical-grade iPSC and their differentiated progeny is the next step in order to prepare for future autologous cell therapy clinical trials. Armed with clinical-grade iPSC, we can then specifically test for their threat of cancer, for proper and efficient differentiation to the correct cell type to treat human disease and then to determine their immunogenicity. Such a rigorous approach sets a far more relevant paradigm for their intended future use than non-clinical-grade iPSC. This review focuses on the latest developments regarding the first possible use of iPSC-derived retinal pigment epithelial cells in treating human disease, covers data gathered on animal models to date and methods to make clinical-grade iPSC, suggests techniques to ensure quality control and discusses possible clinical immune responses.

Identifiers

PMID25984235
PMCPMC4432516
OpenAlexW2141933932

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.