Evidence map›Paper›PMID 25744551›Full record

ArticleImmunology and cell biology2015

Conserved and divergent aspects of human T-cell development and migration in humanized mice.

Joanna Halkias, Bonnie Yen, Kayleigh T Taylor, Olaf Reinhartz, Astar Winoto, Ellen A Robey, Heather J Melichar

Open access · hybridAbstract read
In one paragraph

Article in Immunology and cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
1.8field-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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. FACS-Based Assessment of Human Hematopoietic Stem and Progenitor Cells.International journal of molecular sciences · 2025
    Review
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  6. TFEB controls sensitivity to chemotherapy and immuno-killing in non-small cell lung cancer.Journal of experimental & clinical cancer research : CR · 2024
    Article
  7. Humanized Mouse Models of Bacterial Infections.Antibiotics (Basel, Switzerland) · 2024
    Review
  8. Review
  9. Article
  10. Article
  11. Humanized mouse models for immuno-oncology research.Nature reviews. Clinical oncology · 2023
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Towards gene therapy for IPEX syndrome.European journal of immunology · 2022
    Review
  17. Article
  18. Review
  19. Article
  20. 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

7 authors at 3 institutions in 1 country.

Joanna HalkiasDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, UC Berkeley, Berkeley, CA, USA.
Bonnie YenDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, UC Berkeley, Berkeley, CA, USA.
Kayleigh T TaylorDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, UC Berkeley, Berkeley, CA, USA.
Olaf ReinhartzDivision of Cardiothoracic Surgery, Department of Pediatrics, UCSF Benioff Children's Hospital Oakland, Oakland, CA, USA.
Astar WinotoDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, UC Berkeley, Berkeley, CA, USA.
Ellen A RobeyDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, UC Berkeley, Berkeley, CA, USA.
Heather J MelicharDivision of Immunology and Pathogenesis, Department of Molecular and Cell Biology, UC Berkeley, Berkeley, CA, USA.
University of California, Berkeley · USBerkeley College · USUCSF Benioff Children's Hospital · US

Funding

Signals That Control Thymocyte MigrationR01AI064227 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI ELLEN A ROBEY · 2006 to 2026
$7.4M
NIAID NIH HHS R01 AI064227
6 · The paper itself

Abstract

Humanized mice represent an important model to study the development and function of the human immune system. While it is known that mouse thymic stromal cells can support human T-cell development, the extent of interspecies cross-talk and the degree to which these systems recapitulate normal human T-cell development remain unclear. To address these questions, we compared conventional and non-conventional T-cell development in a neonatal chimera humanized mouse model with that seen in human fetal and neonatal thymus samples, and also examined the impact of a human HLA-A2 transgene expressed by the mouse stroma. Given that dynamic migration and cell-cell interactions are essential for T-cell differentiation, we also studied the intrathymic migration pattern of human thymocytes developing in a murine thymic environment. We found that both conventional T-cell development and intra-thymic migration patterns in humanized mice closely resemble human thymopoiesis. Additionally, we show that developing human thymocytes engage in short, serial interactions with other human hematopoietic-derived cells. However, non-conventional T-cell differentiation in humanized mice differed from both fetal and neonatal human thymopoiesis, including a marked deficiency of Foxp3(+) T-cell development. These data suggest that although the murine thymic microenvironment can support a number of aspects of human T-cell development, important differences remain, and additional human-specific factors may be required.

Indexed as

Cell DifferentiationCell MovementAnimalsBiomarkersCell CommunicationCellular MicroenvironmentGene ExpressionGenes, ReporterHLA-A2 AntigenHumansImmune SystemLymphopoiesisMiceMice, TransgenicModels, AnimalOrganogenesisBiomarkersHLA-A2 Antigen

Identifiers

PMID25744551
PMCPMC4575952
OpenAlexW1968520204

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.