Evidence map›Paper›PMID 31959757›Full record

ArticleNature communications2020

Distinctive phenotypes and functions of innate lymphoid cells in human decidua during early pregnancy.

Oisín Huhn, Martin A Ivarsson, Lucy Gardner, Mike Hollinshead, Jane C Stinchcombe, Puran Chen, Norman Shreeve, Olympe Chazara, Lydia E Farrell, Jakob Theorell and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed, 2 pooled it
8.8field-weighted citation impact, top 2% 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

92 citing papers in PubMed, 2 syntheses or guidelines pooled it, 154 citations in OpenAlex.

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  13. Metabolic Reprogramming Driven by Trophoblasts and Decidual XCR1Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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32 more citing papers are in PubMed but not listed here.

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

17 authors at 6 institutions in 3 countries.

Oisín Huhn *Department of Obstetrics and Gynaecology, University of Cambridge School of Clinical Medicine, National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, CB2 0SW, UK.
Martin A Ivarsson *Department of Pathology, University of Cambridge, Cambridge, CB2 1QP, UK.
Lucy GardnerDepartment of Pathology, University of Cambridge, Cambridge, CB2 1QP, UK.
Mike HollinsheadDepartment of Pathology, University of Cambridge, Cambridge, CB2 1QP, UK.
Jane C StinchcombeCambridge Institute of Medical Research, University of Cambridge, Cambridge, UK.
Puran ChenCenter for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Norman ShreeveDepartment of Obstetrics and Gynaecology, University of Cambridge School of Clinical Medicine, National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, CB2 0SW, UK.
Olympe ChazaraCentre for Trophoblast Research, University of Cambridge, Cambridge, CB2 3EG, UK.
Lydia E FarrellCentre for Trophoblast Research, University of Cambridge, Cambridge, CB2 3EG, UK.ORCID http://orcid.org/0000-0002-7643-6009
Jakob TheorellAutoimmune Neurology Group, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Hormas GhadiallyAstraZeneca, Oncology R&D, Granta Park, Cambridge, CB21 6GH, UK.
Peter ParhamDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Gillian GriffithsCambridge Institute of Medical Research, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-0434-5842
Amir HorowitzPrecision Immunology Institute, Tisch Cancer Institute Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY, 10029, USA.
Ashley MoffettCentre for Trophoblast Research, University of Cambridge, Cambridge, CB2 3EG, UK.ORCID http://orcid.org/0000-0002-8388-9073
Andrew M SharkeyCentre for Trophoblast Research, University of Cambridge, Cambridge, CB2 3EG, UK. as168@cam.ac.uk.ORCID http://orcid.org/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, UK. fc287@medschl.cam.ac.uk.ORCID http://orcid.org/0000-0001-5193-6376
University of Cambridge · GBAstraZeneca (United Kingdom) · GBKarolinska University Hospital · SEIcahn School of Medicine at Mount Sinai · USKarolinska Institutet · SEStanford University · US

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
Medical Research Council MR/P001092/1NIAID NIH HHS R01 AI017892NIAID NIH HHS U01 AI090905Wellcome Trust 200841/Z/16/Z
6 · The paper itself

Abstract

During early pregnancy, decidual innate lymphoid cells (dILCs) interact with surrounding maternal cells and invading fetal extravillous trophoblasts (EVT). Here, using mass cytometry, we characterise five main dILC subsets: decidual NK cells (dNK)1-3, ILC3s and proliferating NK cells. Following stimulation, dNK2 and dNK3 produce more chemokines than dNK1 including XCL1 which can act on both maternal dendritic cells and fetal EVT. In contrast, dNK1 express receptors including Killer-cell Immunoglobulin-like Receptors (KIR), indicating they respond to HLA class I ligands on EVT. Decidual NK have distinctive organisation and content of granules compared with peripheral blood NK cells. Acquisition of KIR correlates with higher granzyme B levels and increased chemokine production in response to KIR activation, suggesting a link between increased granule content and dNK1 responsiveness. Our analysis shows that dILCs are unique and provide specialised functions dedicated to achieving placental development and successful reproduction.

Indexed as

Immunity, InnateAnimalsCell CommunicationChemokines, CDeciduaDendritic CellsFemaleHistocompatibility Antigens Class IHumansK562 CellsKiller Cells, NaturalLymphocyte ActivationLymphocyte SubsetsMicePlacentationPregnancyChemokines, CHistocompatibility Antigens Class IReceptors, KIRXCL1 protein, human

Identifiers

PMID31959757
PMCPMC6971012
OpenAlexW2995215844

What OpenQuestion holds

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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.