Evidence map›Paper›PMID 30249807›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

High-Resolution Genetic and Phenotypic Analysis of KIR2DL1 Alleles and Their Association with Pre-Eclampsia.

Oisín Huhn, Olympe Chazara, Martin A Ivarsson, Christelle Retière, Timothy C Venkatesan, Paul J Norman, Hugo G Hilton, Jyothi Jayaraman, James A Traherne, John Trowsdale and 7 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. The Role of Killer Ig-like Receptors in Diseases from A to Z.International journal of molecular sciences · 2025
    Review
  3. Observational
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  5. Review
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  7. Article
  8. Single-Cell Immunobiology of the Maternal-Fetal Interface.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Following Transplantation for Acute Myelogenous Leukemia, DonorJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 7 countries.

Oisín HuhnDepartment of Obstetrics and Gynaecology, University of Cambridge School of Clinical Medicine, National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge CB2 0SW, United Kingdom.
Olympe ChazaraCentre for Trophoblast Research, University of Cambridge, Cambridge CB2 3EG, United Kingdom.ORCID 0000-0003-0480-7808
Martin A IvarssonCentre for Trophoblast Research, University of Cambridge, Cambridge CB2 3EG, United Kingdom.ORCID 0000-0002-7745-1331
Christelle RetièreEtablissement Français du Sang, Université de Nantes, 44011 Nantes, France.
Timothy C VenkatesanDepartment of Pathology, University of Cambridge, Cambridge CB2 1QP, United Kingdom.ORCID 0000-0002-7733-2308
Paul J NormanDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305.
Hugo G HiltonDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305.ORCID 0000-0003-1488-7194
Jyothi JayaramanCentre for Trophoblast Research, University of Cambridge, Cambridge CB2 3EG, United Kingdom.
James A TraherneDepartment of Pathology, University of Cambridge, Cambridge CB2 1QP, United Kingdom.ORCID 0000-0002-6003-8559
John TrowsdaleCentre for Trophoblast Research, University of Cambridge, Cambridge CB2 3EG, United Kingdom.ORCID 0000-0002-0150-5698
Mitsutero ItoDepartment of Genetics, University of Cambridge, Cambridge CB2 3DY, United Kingdom; and.
Christiane KlingHuman Genetics, MVZ Labor Fenner, D-20095 Hamburg, Germany.ORCID 0000-0002-8809-9708
Peter ParhamDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305.
Hormas GhadiallyMedImmune Ltd., Granta Park, Cambridge CB21 6GH, United Kingdom.
Ashley MoffettCentre for Trophoblast Research, University of Cambridge, Cambridge CB2 3EG, United Kingdom.ORCID 0000-0002-8388-9073
Andrew M SharkeyCentre for Trophoblast Research, University of Cambridge, Cambridge CB2 3EG, United Kingdom; fc287@medschl.cam.ac.uk as168@cam.ac.uk.ORCID 0000-0002-5072-7748
Francesco ColucciDepartment of Obstetrics and Gynaecology, University of Cambridge School of Clinical Medicine, National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge CB2 0SW, United Kingdom; fc287@medschl.cam.ac.uk as168@cam.ac.uk.ORCID 0000-0001-5193-6376
University of Cambridge · GBStanford University · USCentre National de la Recherche Scientifique · FRGranta Design (United Kingdom) · GBKarolinska University Hospital · SEMedizinisches Versorgungszentrum Prof. Mathey, Prof. Schofer · DE

Funding

Insights Into Immune-Related Diseases Born from Population GenomicsU01AI090905 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Paul John Norman · 2010 to 2026
$10.9M
STRUCTURAL BIOLOGY OF HLA-A,B ANTIGENSR01AI017892 · NIAID · STANFORD UNIVERSITY · PI PARHAM, PETER R · 1985 to 2019
$6.1M
Department of HealthMedical Research Council G0901682Medical Research Council MR/P001092/1NIAID NIH HHS R01 AI017892NIAID NIH HHS U01 AI090905Wellcome TrustWellcome Trust 200841/Z/16/Z
6 · The paper itself

Abstract

Killer-cell Ig-like receptor (KIR) genes are inherited as haplotypes. They are expressed by NK cells and linked to outcomes of infectious diseases and pregnancy in humans. Understanding how genotype relates to phenotype is difficult because of the extensive diversity of the KIR family. Indeed, high-resolution KIR genotyping and phenotyping in single NK cells in the context of disease association is lacking. In this article, we describe a new method to separate NK cells expressing allotypes of the KIR2DL1 gene carried by the KIR A haplotype (KIR2DL1A) from those expressing KIR2DL1 alleles carried by the KIR B haplotype (KIR2DL1B). We find that in KIR AB heterozygous individuals, different KIR2DL1 allotypes can be detected in both peripheral blood and uterine NK cells. Using this new method, we demonstrate that both blood and uterine NK cells codominantly express KIR2DL1A and KIR2DL1B allotypes but with a predominance of KIR2DL1A variants, which associate with enhanced NK cell function. In a case-control study of pre-eclampsia, we show that

Indexed as

AllelesAntibodies, MonoclonalCase-Control StudiesCell LineFemaleFlow CytometryGenetic Predisposition to DiseaseHaplotypesHumansKiller Cells, NaturalPre-EclampsiaPregnancyReceptors, KIR2DL1Antibodies, MonoclonalKIR2DL1 protein, humanReceptors, KIR2DL1

Identifiers

PMID30249807
PMCPMC6258046
OpenAlexW2805033265

What OpenQuestion holds

Textmetadata
LicenceTDM
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.