Evidence map›Paper›PMID 31956083›Full record

ArticleStem cell reports2020

iPSC-Based Modeling of RAG2 Severe Combined Immunodeficiency Reveals Multiple T Cell Developmental Arrests.

Maria Themeli, Amiet Chhatta, Hester Boersma, Henk Jan Prins, Martijn Cordes, Edwin de Wilt, Aïda Shahrabi Farahani, Bart Vandekerckhove, Mirjam van der Burg, Rob C Hoeben and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
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  4. Circulating IRF8-expressing CD123Trends in immunology · 2023
    Review
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  8. Frontiers in immunology · 2022
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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

12 authors at 5 institutions in 2 countries.

Maria ThemeliDepartment of Hematology, Amsterdam UMC, Location VUmc, Cancer Center Amsterdam, Amsterdam 1081 HV, The Netherlands.
Amiet ChhattaDepartment of Immunohematology & Blood Transfusion, Leiden University Medical Center, Leiden 2333 ZA, The Netherlands.
Hester BoersmaDepartment of Cell & Chemical Biology, Leiden University Medical Center, Leiden 2300 RC, The Netherlands.
Henk Jan PrinsDepartment of Hematology, Amsterdam UMC, Location VUmc, Cancer Center Amsterdam, Amsterdam 1081 HV, The Netherlands.
Martijn CordesDepartment of Immunohematology & Blood Transfusion, Leiden University Medical Center, Leiden 2333 ZA, The Netherlands.
Edwin de WiltDepartment of Clinical Genetics, Leiden University Medical Center, Leiden 2333 ZC, The Netherlands.
Aïda Shahrabi FarahaniDepartment of Hematology, Amsterdam UMC, Location VUmc, Cancer Center Amsterdam, Amsterdam 1081 HV, The Netherlands.
Bart VandekerckhoveDepartment of Clinical Chemistry, Microbiology and Immunology, Ghent University, Gent 9000, Belgium.
Mirjam van der BurgDepartment of Immunology, Erasmus Medical Center, Rotterdam 3015 GE, The Netherlands.
Rob C HoebenDepartment of Cell & Chemical Biology, Leiden University Medical Center, Leiden 2300 RC, The Netherlands.
Frank J T StaalDepartment of Immunohematology & Blood Transfusion, Leiden University Medical Center, Leiden 2333 ZA, The Netherlands.
Harald M M MikkersDepartment of Cell & Chemical Biology, Leiden University Medical Center, Leiden 2300 RC, The Netherlands; LUMC hiPSC Hotel, Leiden University Medical Center, Leiden 2333 ZC, The Netherlands. Electronic address: h.mikkers@lumc.nl.
Leiden University Medical Center · NLAmsterdam UMC Location VUmc · NLCancer Center AmsterdamErasmus MC · NLGhent University · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RAG2 severe combined immune deficiency (RAG2-SCID) is a lethal disorder caused by the absence of functional T and B cells due to a differentiation block. Here, we generated induced pluripotent stem cells (iPSCs) from a RAG2-SCID patient to study the nature of the T cell developmental blockade. We observed a strongly reduced capacity to differentiate at every investigated stage of T cell development, from early CD7

Indexed as

Models, BiologicalAnimalsAntigens, CDCell DifferentiationCell LineageDNA-Binding ProteinsGene Rearrangement, beta-Chain T-Cell Antigen ReceptorHematopoiesisHumansInduced Pluripotent Stem CellsKiller Cells, NaturalMice, SCIDSevere Combined ImmunodeficiencyT-LymphocytesAntigens, CDDNA-Binding ProteinsV(D)J recombination activating protein 2CD56(+)CD33(+)disease modelingimmunodeficiencyiPSCNK cellsRAGSCIDT cell development

Identifiers

PMID31956083
PMCPMC7013232
OpenAlexW2999677852

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.