Evidence map›Paper›PMID 26195040›Full record

ArticleNature communications2015

Active suppression of intestinal CD4(+)TCRαβ(+) T-lymphocyte maturation during the postnatal period.

Natalia Torow, Kai Yu, Kasra Hassani, Jenny Freitag, Olga Schulz, Marijana Basic, Anne Brennecke, Tim Sparwasser, Norbert Wagner, André Bleich and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

50 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
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  6. T-bet-expressing Tr1 cells driven by dietary signals dominate the small intestinal immune landscape.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  8. Article
  9. Review
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  11. Review
  12. Review
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  15. Intraepithelial Lymphocytes of the Intestine.Annual review of immunology · 2024
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Article
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

15 authors at 4 institutions in 1 country.

Natalia Torow1] Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany [2] Institute of Medical Microbiology, RWTH University Hospital, Pauwelsstraße 30, 52074 Aachen, Germany.
Kai YuInstitute of Immunology, Hannover Medical School, Hannover, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
Kasra HassaniInstitute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
Jenny FreitagInstitute of Infection Immunology, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Medical School, Hannover (MHH) and the Helmholtz Centre for Infection Research (HZI), Feodor-Lynen-Straße 7, 30625 Hannover, Germany.
Olga SchulzInstitute of Immunology, Hannover Medical School, Hannover, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
Marijana BasicInstitute for Laboratory Animal Science, Hannover Medical School, Hannover, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
Anne BrenneckeDepartment of Molecular Immunology, Helmholtz Centre for Infection Research, Inhoffenstraße 7, 38124 Braunschweig, Germany.
Tim SparwasserInstitute of Infection Immunology, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Medical School, Hannover (MHH) and the Helmholtz Centre for Infection Research (HZI), Feodor-Lynen-Straße 7, 30625 Hannover, Germany.
Norbert WagnerDepartment of Pediatrics, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074 Aachen, Germany.
André BleichInstitute for Laboratory Animal Science, Hannover Medical School, Hannover, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
Matthias LochnerInstitute of Infection Immunology, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Medical School, Hannover (MHH) and the Helmholtz Centre for Infection Research (HZI), Feodor-Lynen-Straße 7, 30625 Hannover, Germany.
Siegfried WeissDepartment of Molecular Immunology, Helmholtz Centre for Infection Research, Inhoffenstraße 7, 38124 Braunschweig, Germany.
Reinhold FörsterInstitute of Immunology, Hannover Medical School, Hannover, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
Oliver Pabst1] Institute of Immunology, Hannover Medical School, Hannover, Carl-Neuberg-Straße 1, 30625 Hannover, Germany [2] Institute of Molecular Medicine RWTH Aachen University Hospital, Pauwelsstraße 30, 52074 Aachen, Germany.
Mathias W Hornef1] Institute of Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany [2] Institute of Medical Microbiology, RWTH University Hospital, Pauwelsstraße 30, 52074 Aachen, Germany.
Medizinische Hochschule Hannover · DEHelmholtz Centre for Infection Research · DERWTH Aachen University · DECenter for Experimental and Clinical Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Priming of the mucosal immune system during the postnatal period substantially influences host-microbial interaction and susceptibility to immune-mediated diseases in adult life. The underlying mechanisms are ill defined. Here we show that shortly after birth, CD4 T cells populate preformed lymphoid structures in the small intestine and quickly acquire a distinct transcriptional profile. T-cell recruitment is independent of microbial colonization and innate or adaptive immune stimulation but requires β7 integrin expression. Surprisingly, neonatal CD4 T cells remain immature throughout the postnatal period under homeostatic conditions but undergo maturation and gain effector function on barrier disruption. Maternal SIgA and regulatory T cells act in concert to prevent immune stimulation and maintain the immature phenotype of CD4 T cells in the postnatal intestine during homeostasis. Active suppression of CD4 T-cell maturation during the postnatal period might contribute to prevent auto-reactivity, sustain a broad TCR repertoire and establish life-long immune homeostasis.

Indexed as

Immunity, MucosalAnimalsAnimals, NewbornCD4-Positive T-LymphocytesGrowth and DevelopmentImmunophenotypingIntestinesMice, Transgenic

Identifiers

PMID26195040
PMCPMC4518322
OpenAlexW2267072039

What OpenQuestion holds

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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.