Evidence map›Paper›PMID 23335954›Full record

ArticlePloS one2013

The murine Th2 locus undergoes epigenetic modification in the thymus during fetal and postnatal ontogeny.

Momoko Yoshimoto, Mervin C Yoder, Patricia Guevara, Becky Adkins

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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Human CD36Immunology · 2021
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Human Naive T Cells Express Functional CXCL8 and Promote Tumorigenesis.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  13. Review
  14. Immune responses in neonates.Expert review of clinical immunology · 2014
    Review
  15. 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

4 authors.

Momoko YoshimotoHerman B. Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Mervin C Yoder
Patricia Guevara
Becky Adkins

Funding

Regulation of murine neonatal Th2 functionR01AI044923 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ADKINS, REBECCA D · 2000 to 2010
$3.3M
Lymphopoietic development in the extra-embryonic yolk sacR01AI080759 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI YODER, MERVIN C. · 2009 to 2013
$1.8M
Developmentally regulated epigenetic programs in fetal/neonatal T lineage cellsR56AI044923 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ADKINS, REBECCA D · 2011 to 2011
$446k
NIAID NIH HHS AI044923NIAID NIH HHS AI080759NIAID NIH HHS R01 AI044923NIAID NIH HHS R01 AI080759NIAID NIH HHS R56 AI044923
6 · The paper itself

Abstract

Epigenetic modifications play a central role in the differentiation and function of immune cells in adult animals. Developmentally regulated epigenetic patterns also appear to contribute to the ontogeny of the immune system. We show here that the epigenetic profile of the T-helper (Th) 2 locus undergoes changes in T lineage cells beginning in mid-gestation and extending throughout the first week of life. In particular, regulatory regions of the Th2 locus are largely methylated at CpG residues among fetal liver common lymphoid progenitor cells. The locus subsequently becomes highly hypomethylated among the downstream progeny of these cells within the fetal thymus. This hypomethylated state is preserved until birth when the locus becomes rapidly re-methylated, achieving adult-like status by 3-6 days post birth. Notably, the capacity for rapid, high level Th2 cytokine production is lost in parallel with this re-methylation. In vitro organ culture and in vivo transplantation experiments indicate that signals from the adult environment are required to achieve the postnatal methylated state. Together, these findings indicate that the Th2 bias of neonates may be conferred, in part, by an epigenetic profile inherited from fetal life. However, the fetal program is rapidly terminated post birth by the development of signals leading to the acquisition of adult-like epigenetic patterns.

Indexed as

Epigenesis, GeneticGene Expression Regulation, DevelopmentalAnimalsCD4-Positive T-LymphocytesCell LineageCytokinesDNA MethylationEnvironmentFemaleGene-Environment InteractionGene OrderGenetic LociHistonesLymphoid Progenitor CellsMiceMice, TransgenicCytokinesHistones

Identifiers

PMID23335954
PMCPMC3546009

What OpenQuestion holds

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Registered trials

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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.