Evidence map›Paper›PMID 27241697›Full record

ArticleImmunology and cell biology2016

The majority of murine γδ T cells at the maternal-fetal interface in pregnancy produce IL-17.

Gabriela V Pinget, Theresa M Corpuz, Jessica Stolp, Erin L Lousberg, Kerrilyn R Diener, Sarah A Robertson, Jonathan Sprent, Kylie E Webster

Abstract read
PubMed Publisher
In one paragraph

Article in Immunology and cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 55 citations in OpenAlex.

  1. Observational
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. A Framework for Understanding Maternal Immunity.Immunology and allergy clinics of North America · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Hijacking Sexual Immuno-Privilege in GBM-An Immuno-Evasion Strategy.International journal of molecular sciences · 2021
    Article
  19. γδ T cells in tissue physiology and surveillance.Nature reviews. Immunology · 2021
    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

8 authors at 5 institutions in 1 country.

Gabriela V PingetImmunology Division, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Theresa M CorpuzImmunology Division, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Jessica StolpImmunology Division, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Erin L LousbergThe Robinson Research Institute and School of Medicine, University of Adelaide, Adelaide, SA, Australia.
Kerrilyn R DienerThe Robinson Research Institute and School of Medicine, University of Adelaide, Adelaide, SA, Australia.
Sarah A RobertsonThe Robinson Research Institute and School of Medicine, University of Adelaide, Adelaide, SA, Australia.
Jonathan SprentImmunology Division, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Kylie E WebsterImmunology Division, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Garvan Institute of Medical Research · AUHanson Institute · AUSt Vincent's Clinic · AUUniversity of Adelaide · AUUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Compared with lymphoid tissues, the immune cell compartment at mucosal sites is enriched with T cells bearing the γδ T-cell receptor (TCR). The female reproductive tract, along with the placenta and uterine decidua during pregnancy, are populated by γδ T cells predominantly expressing the invariant Vγ6(+)Vδ1(+) receptor. Surprisingly little is understood about the function of these cells. We found that the majority of γδ T cells in the non-pregnant uterus, pregnant uterus, decidua and placenta of mice express the transcription factor RORγt and produce interleukin-17 (IL-17). In contrast, IFNγ-producing γδ T cells were markedly reduced in gestational tissues compared with uterine-draining lymph nodes and spleen. Both uterine-resident invariant Vγ6(+) and Vγ4(+) γδ T cells which are more typically found in lymphoid tissues and circulating blood, were found to express IL-17. Vγ4(+) γδ T cells were particularly enriched in the placenta, suggesting a pregnancy-specific recruitment or expansion of these cells. A small increase in IL-17-producing γδ T cells was observed in allogeneic compared with syngeneic pregnancy, suggesting a contribution to regulating the maternal response to paternally-derived alloantigens. However, their high proportions also in non-pregnant uteri and gestational tissues of syngeneic pregnancy imply a role in the prevention of intrauterine infection or quality control of fetal development. These data suggest the need for a more rigorous evaluation of the role of IL-17 in sustaining normal pregnancy, particularly as emerging data points to a pathogenic role for IL-17 in pre-eclampsia, pre-term birth, miscarriage and maternal immune activation-induced behavioral abnormalities in offspring.

Indexed as

AnimalsFemaleInterleukin-17Maternal-Fetal ExchangeMice, Inbred C57BLMice, Inbred DBANuclear Receptor Subfamily 1, Group F, Member 3PlacentaPregnancyReceptors, Antigen, T-Cell, gamma-deltaT-LymphocytesUterusInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3Receptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID27241697
OpenAlexW2410987774

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.