Evidence map›Paper›PMID 21665273›Full record

ArticlePlacenta2011

How does variability of immune system genes affect placentation?

F Colucci, S Boulenouar, J Kieckbusch, A Moffett

Open access · hybridAbstract read
In one paragraph

Article in Placenta, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-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

21 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  11. The role of the maternal immune system in the regulation of human birthweight.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  12. Review
  13. Pathophysiology of ischemic placental disease.Seminars in perinatology · 2014
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. The role of the invasive, placental trophoblast in human pregnancy.Wiener medizinische Wochenschrift (1946) · 2012
    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

4 authors at 1 institution in 1 country.

F ColucciDepartment of Obstetrics and Gynaecology, University of Cambridge Clinical School, The Rosie Hospital, Cambridge, UK. fc287@medschl.cam.ac.uk
S Boulenouar
J Kieckbusch
A Moffett
University of Cambridge · GB

Funding

Medical Research Council G0900101Wellcome Trust
6 · The paper itself

Abstract

Formation of the placenta is a crucial step in mammalian pregnancy. Apart from its function in ensuring an optimal supply of nutrients and oxygen to the fetus, the placenta is also the interface at which allo-recognition of invading trophoblast cells by the maternal immune system can potentially occur. We summarise here the "state of the art" on how variability of immune system genes that code for major histocompatibility complex (MHC) molecules and natural killer receptors (NKR) may impact on human placentation. MHC and NKR are the most polymorphic human genes. Our recent reports point out that specific combinations of fetal MHC and maternal NKR genes in humans correlate with the risk of pre-eclampsia, recurrent miscarriage (RM) and fetal growth restriction (FGR). Research in this field is still at an early stage and future studies in mouse and humans will be needed before the results can be translated to clinical applications. We discuss our recent work, as well as the opportunities offered by mouse genetics, to understand the cellular and molecular mechanisms underlying immune interactions at the maternal-fetal interface.

Indexed as

Abortion, HabitualAnimalsFemaleGenes, MHC Class IIHumansKiller Cells, NaturalMajor Histocompatibility ComplexMiceModels, AnimalPlacentaPlacentationPre-EclampsiaPregnancyReceptors, Natural Killer CellUterusReceptors, Natural Killer Cell

Identifiers

PMID21665273
PMCPMC3202627
OpenAlexW2075581297

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.