Evidence map›Paper›PMID 23585844›Full record

ArticlePloS one2013

In vivo expansion of co-transplanted T cells impacts on tumor re-initiating activity of human acute myeloid leukemia in NSG mice.

Malte von Bonin, Martin Wermke, Kadriye Nehir Cosgun, Christian Thiede, Martin Bornhauser, Gerard Wagemaker, Claudia Waskow

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Article
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  8. In Vivo Murine-Matured Human CD3Molecular therapy. Methods & clinical development · 2017
    Article
  9. A three-dimensionalHaematologica · 2017
    Article
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  11. Article
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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

7 authors.

Malte von BoninRegeneration in Hematopoiesis, Center for Regenerative Therapies Dresden - CRTD, DFG Research Center and Cluster of Excellence, Technische Universität Dresden, Dresden, Germany.
Martin Wermke
Kadriye Nehir Cosgun
Christian Thiede
Martin Bornhauser
Gerard Wagemaker
Claudia Waskow

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cells from acute myeloid leukemia (AML) patients are frequently transplanted into immune-compromised mouse strains to provide an in vivo environment for studies on the biology of the disease. Since frequencies of leukemia re-initiating cells are low and a unique cell surface phenotype that includes all tumor re-initiating activity remains unknown, the underlying mechanisms leading to limitations in the xenotransplantation assay need to be understood and overcome to obtain robust engraftment of AML-containing samples. We report here that in the NSG xenotransplantation assay, the large majority of mononucleated cells from patients with AML fail to establish a reproducible myeloid engraftment despite high donor chimerism. Instead, donor-derived cells mainly consist of polyclonal disease-unrelated expanded co-transplanted human T lymphocytes that induce xenogeneic graft versus host disease and mask the engraftment of human AML in mice. Engraftment of mainly myeloid cell types can be enforced by the prevention of T cell expansion through the depletion of lymphocytes from the graft prior transplantation.

Indexed as

AdultAgedAnimalsBone Marrow TransplantationCell ProliferationFemaleGraft vs Host DiseaseHumansLeukemia, Myeloid, AcuteLymphocyte DepletionMaleMiceMice, Inbred NODMice, SCIDMiddle AgedMyeloid Cells

Identifiers

PMID23585844
PMCPMC3621959

What OpenQuestion holds

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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.