Evidence map›Paper›PMID 28963568›Full record

ArticleScientific reports2017

Targeted genome editing restores T cell differentiation in a humanized X-SCID pluripotent stem cell disease model.

Jamal Alzubi, Celeste Pallant, Claudio Mussolino, Steven J Howe, Adrian J Thrasher, Toni Cathomen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
0.8field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Modeling MyD88 DeficiencyFrontiers in immunology · 2020
    Article
  4. Review
  5. Article
  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

6 authors at 3 institutions in 2 countries.

Jamal AlzubiInstitute for Transfusion Medicine and Gene Therapy, Medical Center - University of Freiburg, Freiburg, Germany.
Celeste PallantInstitute of Child Health, University College London, London, United Kingdom.
Claudio MussolinoInstitute for Transfusion Medicine and Gene Therapy, Medical Center - University of Freiburg, Freiburg, Germany.
Steven J HoweInstitute of Child Health, University College London, London, United Kingdom.
Adrian J ThrasherInstitute of Child Health, University College London, London, United Kingdom.
Toni CathomenInstitute for Transfusion Medicine and Gene Therapy, Medical Center - University of Freiburg, Freiburg, Germany. toni.cathomen@uniklinik-freiburg.de.ORCID 0000-0002-7757-4630
University of Freiburg · DEAge UK · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GB

Funding

Medical Research CouncilWellcome Trust
6 · The paper itself

Abstract

The generation of T cells from pluripotent stem cells (PSCs) is attractive for investigating T cell development and validating genome editing strategies in vitro. X-linked severe combined immunodeficiency (X-SCID) is an immune disorder caused by mutations in the IL2RG gene and characterised by the absence of T and NK cells in patients. IL2RG encodes the common gamma chain, which is part of several interleukin receptors, including IL-2 and IL-7 receptors. To model X-SCID in vitro, we generated a mouse embryonic stem cell (ESC) line in which a disease-causing human IL2RG gene variant replaces the endogenous Il2rg locus. We developed a stage-specific T cell differentiation protocol to validate genetic correction of the common G691A mutation with transcription activator-like effector nucleases. While all ESC clones could be differentiated to hematopoietic precursor cells, stage-specific analysis of T cell maturation confirmed early arrest of T cell differentiation at the T cell progenitor stage in X-SCID cells. In contrast, genetically corrected ESCs differentiated to CD4 + or CD8 + single-positive T cells, confirming correction of the cellular X-SCID phenotype. This study emphasises the value of PSCs for disease modelling and underlines the significance of in vitro models as tools to validate genome editing strategies before clinical application.

Indexed as

Amino Acid SubstitutionAnimalsCell DifferentiationDisease Models, AnimalGene EditingGene ExpressionHematopoietic Stem CellsHumansInterleukin-2Interleukin-7Interleukin Receptor Common gamma SubunitKiller Cells, NaturalMiceMice, SCIDMice, TransgenicMolecular Targeted TherapyIL2RG protein, humanInterleukin-2Interleukin-7interleukin-7, mouseInterleukin Receptor Common gamma SubunitTranscription Activator-Like Effector Nucleases

Identifiers

PMID28963568
PMCPMC5622068
OpenAlexW2760736354

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.