Evidence map›Paper›PMID 21037088›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Cutting edge: adaptive versus innate receptor signals selectively control the pool sizes of murine IFN-γ- or IL-17-producing γδ T cells upon infection.

Julie C Ribot, Miguel Chaves-Ferreira, Francisco d'Orey, Mélanie Wencker, Natacha Gonçalves-Sousa, Jérémie Decalf, João P Simas, Adrian C Hayday, Bruno Silva-Santos

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

53 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. IL-27 maintains cytotoxic Ly6CThe EMBO journal · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. γδT Cells Are Required for CD8Frontiers in immunology · 2021
    Article
  14. Article
  15. Review
  16. β2 Integrins differentially regulate γδ T cell subset thymic development and peripheral maintenance.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  17. Article
  18. γδ-T cells promote IFN-γ-dependentProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  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

9 authors at 5 institutions in 4 countries.

Julie C RibotInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa.
Miguel Chaves-Ferreira *Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa.
Francisco d'Orey *Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa.
Mélanie WenckerLondon Research Institute, Cancer Research UK, Lincoln's Inn Fields.
Natacha Gonçalves-SousaInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa.
Jérémie DecalfInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa.
João P SimasInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa.
Adrian C HaydayLondon Research Institute, Cancer Research UK, Lincoln's Inn Fields.
Bruno Silva-SantosInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa.
University of Lisbon · PTInstituto de Medicina Tropical · PYInstituto Gulbenkian de Ciência · PTCancer Research UK · GBKing's College - North Carolina · US

Funding

Wellcome Trust 085780
6 · The paper itself

Abstract

γδ T lymphocytes are commonly viewed as embracing properties of both adaptive and innate immunity. Contributing to this is their responsiveness to pathogen products, either with or without the involvement of the TCR and its coreceptors. This study clarifies this paradoxical behavior by showing that these two modes of responsiveness are the properties of two discrete sets of murine lymphoid γδ T cells. Thus, MyD88 deficiency severely impaired the response to malaria infection of CD27((-)), IL-17A-producing γδ T cells, but not of IFN-γ-producing γδ cells. Instead, the latter compartment was severely contracted by ablating CD27, which synergizes with TCRγδ in the induction of antiapoptotic mediators and cell cycle-promoting genes in CD27((+)), IFN-γ-secreting γδ T cells. Hence, innate versus adaptive receptors differentially control the peripheral pool sizes of discrete proinflammatory γδ T cell subsets during immune responses to infection.

Indexed as

Adaptive ImmunityImmunity, InnateAnimalsCells, CulturedCell SurvivalCoculture TechniquesInterferon-gammaInterleukin-17Lymphocyte ActivationLymphocyte CountMiceMice, Inbred C57BLMice, KnockoutPlasmodium bergheiReceptors, Antigen, T-Cell, gamma-deltaRhadinovirusInterferon-gammaInterleukin-17Receptors, Antigen, T-Cell, gamma-deltaTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID21037088
PMCPMC3915338
OpenAlexW2126608150

What OpenQuestion holds

Textmetadata
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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.