Evidence map›Paper›PMID 29503198›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2018

Efficient Non-viral Gene Delivery into Human Hematopoietic Stem Cells by Minicircle Sleeping Beauty Transposon Vectors.

Marta Holstein, Cristina Mesa-Nuñez, Csaba Miskey, Elena Almarza, Valentina Poletti, Marco Schmeer, Esther Grueso, Juan Carlos Ordóñez Flores, Dennis Kobelt, Wolfgang Walther and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
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  7. Current Non-Viral-Based Strategies to Manufacture CAR-T Cells.International journal of molecular sciences · 2024
    Review
  8. A novel hyperactive variant of theMolecular therapy. Nucleic acids · 2024
    Article
  9. Article
  10. Article
  11. Engineering of potent CAR NK cells using non-viral Sleeping Beauty transposition from minimalistic DNA vectors.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  12. Review
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  18. Review
  19. Article
  20. Automated, scaled, transposon-based production of CAR T cells.Journal for immunotherapy of cancer · 2022
    Article
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

20 authors at 8 institutions in 4 countries.

Marta HolsteinTransposition and Genome Engineering, Division of Medical Biotechnology, Paul Ehrlich Institute, Langen, Germany.
Cristina Mesa-NuñezDivision of Hematopoietic Innovative Therapies, Centro de Investigaciones Energéticas Medioambientales y Tecnológicas and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIEMAT/CIBERER), Madrid, Spain; Advanced Therapies Unit, Instituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD, UAM) Madrid, Spain.
Csaba MiskeyTransposition and Genome Engineering, Division of Medical Biotechnology, Paul Ehrlich Institute, Langen, Germany.
Elena AlmarzaDivision of Hematopoietic Innovative Therapies, Centro de Investigaciones Energéticas Medioambientales y Tecnológicas and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIEMAT/CIBERER), Madrid, Spain; Advanced Therapies Unit, Instituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD, UAM) Madrid, Spain.
Valentina PolettiGenethon, Evry, France.
Marco SchmeerPlasmidFactory GmbH & Co. KG, Bielefeld, Germany.
Esther GruesoTransposition and Genome Engineering, Division of Medical Biotechnology, Paul Ehrlich Institute, Langen, Germany.
Juan Carlos Ordóñez FloresTransposition and Genome Engineering, Division of Medical Biotechnology, Paul Ehrlich Institute, Langen, Germany.
Dennis KobeltTranslational Oncology, Experimental and Clinical Research Center, Charité University Medicine, Berlin, Germany.
Wolfgang WaltherTranslational Oncology, Experimental and Clinical Research Center, Charité University Medicine, Berlin, Germany.
Manish K Anejaethris GmbH, Planegg, Germany.
Johannes Geigerethris GmbH, Planegg, Germany.
Halvard B BonigDepartment of Transfusion Medicine and Immunohematology, Johann-Wolfgang-Goethe Universität, Frankfurt, Germany.
Zsuzsanna IzsvákMobile DNA, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
Martin SchleefPlasmidFactory GmbH & Co. KG, Bielefeld, Germany.
Carsten Rudolphethris GmbH, Planegg, Germany; Department of Pediatrics, Ludwig Maximilian University, Munich, Germany.
Fulvio MavilioGenethon, Evry, France; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Juan A BuerenDivision of Hematopoietic Innovative Therapies, Centro de Investigaciones Energéticas Medioambientales y Tecnológicas and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIEMAT/CIBERER), Madrid, Spain; Advanced Therapies Unit, Instituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD, UAM) Madrid, Spain.
Guillermo GuenecheaDivision of Hematopoietic Innovative Therapies, Centro de Investigaciones Energéticas Medioambientales y Tecnológicas and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIEMAT/CIBERER), Madrid, Spain; Advanced Therapies Unit, Instituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD, UAM) Madrid, Spain.
Zoltán IvicsTransposition and Genome Engineering, Division of Medical Biotechnology, Paul Ehrlich Institute, Langen, Germany. Electronic address: zoltan.ivics@pei.de.
Paul Ehrlich Institut · DEEthris (Germany) · DECentre for Biomedical Network Research on Rare Diseases · ESCharité - Universitätsmedizin Berlin · DEGenethon (France) · FRHospital Universitario Fundación Jiménez Díaz · ESGoethe University Frankfurt · DEMax Delbrück Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Sleeping Beauty (SB) transposon system is a non-viral gene delivery platform that combines simplicity, inexpensive manufacture, and favorable safety features in the context of human applications. However, efficient correction of hematopoietic stem and progenitor cells (HSPCs) with non-viral vector systems, including SB, demands further refinement of gene delivery techniques. We set out to improve SB gene transfer into hard-to-transfect human CD34

Indexed as

DNA Transposable ElementsGene Transfer TechniquesAnimalsCell SurvivalFlow CytometryGene ExpressionGenetic VectorsHematopoietic Stem CellsHumansMiceMice, KnockoutRetroviridaeTransfectionTransgenesDNA Transposable Elementschromosomal integrationgene therapygene vectorshematopoietic stem cellsnonviral gene deliverytransposition

Identifiers

PMID29503198
PMCPMC6079369
OpenAlexW2783858895

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.