Evidence map›Paper›PMID 26065585›Full record

ReviewNature reviews. Immunology2015

Transcriptional regulation of innate lymphoid cell fate.

Nicolas Serafini, Christian A J Vosshenrich, James P Di Santo

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 177 papers.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed
18.5field-weighted citation impact, top 1% 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

177 citing papers in PubMed, 276 citations in OpenAlex.

  1. Article
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  15. The role of trained immunity in sepsis.Frontiers in immunology · 2024
    Review
  16. The Function of E2A in B-Cell Development.Advances in experimental medicine and biology · 2024
    Review
  17. Article
  18. Article
  19. CD45 alleviates airway inflammation and lung fibrosis by limiting expansion and activation of ILC2s.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. Review

117 more citing papers are in PubMed but not listed here.

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 1 country.

Nicolas SerafiniInnate Immunity Unit, Institut Pasteur, Paris 75015, and the Institut National de la Santé et de la Recherche Médicale (INSERM) U668, Paris 75015, France.
Christian A J VosshenrichInnate Immunity Unit, Institut Pasteur, Paris 75015, and the Institut National de la Santé et de la Recherche Médicale (INSERM) U668, Paris 75015, France.
James P Di SantoInnate Immunity Unit, Institut Pasteur, Paris 75015, and the Institut National de la Santé et de la Recherche Médicale (INSERM) U668, Paris 75015, France.
Institut Pasteur · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innate lymphoid cells (ILCs) are a recently described family of lymphoid effector cells that have important roles in immune defence, inflammation and tissue remodelling. It has been proposed that ILCs represent 'innate' homologues of differentiated effector T cells, and they have been categorized into three groups — namely, ILC1s, ILC2s and ILC3s — on the basis of their expression of cytokines and transcription factors that are typically associated with T helper 1 (T(H)1)-, T(H)2- and T(H)17-type immune responses, respectively. Indeed, remarkable similarity is seen between the specific transcription factors required for the development and diversification of different ILC groups and those that drive effector T cell differentiation. The recent identification of dedicated ILC precursors has provided a view of the mechanisms that control this first essential stage of ILC development. Here, we discuss the transcriptional mechanisms that regulate ILC development and diversification into distinct effector subsets with key roles in immunity and tissue homeostasis. We further caution against the current distinction between 'helper' versus 'killer' subsets in the evolving area of ILC nomenclature.

Indexed as

Cell LineageAnimalsCell DifferentiationHumansImmunity, InnateLymphocytesTranscription, Genetic

Identifiers

PMID26065585
OpenAlexW1511974199

What OpenQuestion holds

Textmetadata
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.