Evidence map›Paper›PMID 24367369›Full record

ReviewFrontiers in immunology2013

Molecular Mechanisms of Differentiation of Murine Pro-Inflammatory γδ T Cell Subsets.

Karine Serre, Bruno Silva-Santos

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. γδ T Cells and Allergic Diseases.Clinical reviews in allergy & immunology · 2023
    Review
  6. Intestinal commensal microbiota and cytokines regulate Fut2Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Adjustments of γδ T Cells in the Lung ofFrontiers in immunology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. IL-17Nature immunology · 2017
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. PLZF Controls the Development of Fetal-Derived IL-17+Vγ6+ γδ T Cells.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  20. Immune mechanisms in acetaminophen-induced acute liver failure.Hepatobiliary surgery and nutrition · 2014
    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

2 authors.

Karine SerreFaculdade de Medicina, Instituto de Medicina Molecular, Universidade de Lisboa , Lisbon , Portugal.
Bruno Silva-SantosFaculdade de Medicina, Instituto de Medicina Molecular, Universidade de Lisboa , Lisbon , Portugal.

Funding

European Research Council 260352
6 · The paper itself

Abstract

γδ T cells are unconventional innate-like lymphocytes that actively participate in protective immunity against tumors and infectious organisms including bacteria, viruses, and parasites. However, γδ T cells are also involved in the development of inflammatory and autoimmune diseases. γδ T cells are functionally characterized by very rapid production of pro-inflammatory cytokines, while also impacting on (slower but long-lasting) adaptive immune responses. This makes it crucial to understand the molecular mechanisms that regulate γδ T cell effector functions. Although they share many similarities with αβ T cells, our knowledge of the molecular pathways that control effector functions in γδ T cells still lags significantly behind. In this review, we focus on the segregation of interferon-γ versus interleukin-17 production in murine thymic-derived γδ T cell subsets defined by CD27 and CCR6 expression levels. We summarize the most recent studies that disclose the specific epigenetic and transcriptional mechanisms that govern the stability or plasticity of discrete pro-inflammatory γδ T cell subsets, whose manipulation may be valuable for regulating (auto)immune responses.

Indexed as

cytokinesinterferon-γinterleukin-17T cell differentiationtranscription factorsγδ T cells

Identifiers

PMID24367369
PMCPMC3852037

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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.