Evidence map›Paper›PMID 32055644›Full record

ArticleMolecular therapy. Methods & clinical development2020

Human iPSC-Derived Neural Crest Stem Cells Exhibit Low Immunogenicity.

Vera J Mehler, Chris J Burns, Hans Stauss, Robert J Francis, Melanie L Moore

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

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  15. Maintenance of Hypoimmunogenic FeaturesFrontiers in bioengineering and biotechnology · 2022
    Article
  16. Article
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  19. Neural crest-like stem cells for tissue regeneration.Stem cells translational medicine · 2021
    Review
  20. 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

5 authors at 2 institutions in 1 country.

Vera J MehlerEndocrinology Section, Biotherapeutics, National Institute for Biological Standards and Control (NIBSC), Blanche Lane, Potters Bar EN6 3QG, UK.
Chris J BurnsEndocrinology Section, Biotherapeutics, National Institute for Biological Standards and Control (NIBSC), Blanche Lane, Potters Bar EN6 3QG, UK.
Hans StaussDivision of Infection and Immunity, University College London, Gower Street, London WC1E 6BT, UK.
Robert J FrancisBiological Imaging Group, Analytical and Biological Sciences, NIBSC, Blanche Lane, Potters Bar EN6 3QG, UK.
Melanie L MooreEndocrinology Section, Biotherapeutics, National Institute for Biological Standards and Control (NIBSC), Blanche Lane, Potters Bar EN6 3QG, UK.
National Institute for Biological Standards and Control · GBUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent clinical trials are evaluating induced pluripotent stem cells (iPSCs) as a cellular therapy in the field of regenerative medicine. The widespread clinical utility of iPSCs is expected to be realized using allogeneic cells that have undergone thorough safety evaluations, including assessment of their immunogenicity. IPSC-derived neural crest stem cells (NCSCs) have significant potential in regenerative medicine; however, their application in cellular therapy has not been widely studied to date, and no reports on their potential immunogenicity have been published so far. In this study, we have assessed the expression of immune-related antigens in iPSC-NCSCs, including human leukocyte antigen (HLA) class I and II and co-stimulatory molecules. To investigate functional immunogenicity, we used iPSC-NCSCs as stimulator cells in a one-way mixed lymphocyte reaction. In these experiments, iPSC-NCSCs did not stimulate detectable proliferation of CD3

Identifiers

PMID32055644
PMCPMC7005462
OpenAlexW3000742147

What OpenQuestion 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 OpenQuestion graph.