Evidence map›Paper›PMID 30395373›Full record

ReviewStem cells (Dayton, Ohio)2019

Concise Review: Exploring Immunomodulatory Features of Mesenchymal Stromal Cells in Humanized Mouse Models.

Vera J Mehler, Chris Burns, Melanie L Moore

Open access · hybridAbstract readReview
In one paragraph

Review in Stem cells (Dayton, Ohio), 2019. 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
2.2field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
  6. A Monocytic Barrier to the Humanization of Immunodeficient Mice.Current stem cell research & therapy · 2024
    Review
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  8. Article
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  12. 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

3 authors at 2 institutions in 2 countries.

Vera J MehlerEndocrinology Section, Biotherapeutics, National Institute for Biological Standards and Control, South Mimms, United Kingdom.ORCID 0000-0003-4614-7393
Chris BurnsEndocrinology Section, Biotherapeutics, National Institute for Biological Standards and Control, South Mimms, United Kingdom.
Melanie L MooreEndocrinology Section, Biotherapeutics, National Institute for Biological Standards and Control, South Mimms, United Kingdom.
National Institute for Biological Standards and Control · GBInstitute of Infection and Immunity · CA

Funding

Department of Health 044/0069
6 · The paper itself

Abstract

With their immunosuppressive features, human mesenchymal stromal cells (MSCs), sometimes also termed as mesenchymal stem cells, hold great potential as a cell-based therapy for various immune-mediated diseases. Indeed, MSCs have already been approved as a treatment for graft versus host disease. However, contradictory data from clinical trials and lack of conclusive proof of efficacy hinder the progress toward wider clinical use of MSCs and highlight the need for more relevant disease models. Humanized mice are increasingly used as models to study immune-mediated disease, as they simulate human immunobiology more closely than conventional murine models. With further advances in their resemblance to human immunobiology, it is very likely that humanized mice will be used more commonly as models to investigate MSCs with regard to their therapeutic safety and their immunomodulatory effect and its underlying mechanisms. Recent studies that explore the immunosuppressive features of MSCs in humanized mouse models will be discussed in this review. Stem Cells 2019;37:298-305.

Indexed as

Disease Models, AnimalGraft vs Host DiseaseImmune System DiseasesImmunomodulationMesenchymal Stem CellsMesenchymal Stem Cell TransplantationAnimalsHumansMiceCell therapyGraft versus host diseaseHuman immune systemHumanized mouseImmunomodulationImmunosuppressionMesenchymal stem cells

Identifiers

PMID30395373
PMCPMC6446739
OpenAlexW2900372339

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.