Evidence map›Paper›PMID 26460007›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

The HLA-G cycle provides for both NK tolerance and immunity at the maternal-fetal interface.

Tamara Tilburgs, J Henry Evans, Ângela C Crespo, Jack L Strominger

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

94 citing papers in PubMed, 1 synthesis or guideline pooled it, 166 citations in OpenAlex.

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  9. HLA-G, IL-6 and TGF-β in Seminal Plasma as Potential Biomarkers of ART Outcome.American journal of reproductive immunology (New York, N.Y. : 1989) · 2025
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34 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

4 authors at 1 institution in 2 countries.

Tamara TilburgsDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138; tilburgs@fas.harvard.edu jlstrom@fas.harvard.edu.
J Henry EvansDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138;
Ângela C CrespoDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138; Doctoral Programme in Experimental Biology and Biomedicine, Center for Neuroscience and Cell Biology, University of Coimbra, 3004-504 Coimbra, Portugal.ORCID http://orcid.org/0000-0002-6731-8190
Jack L StromingerDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138; tilburgs@fas.harvard.edu jlstrom@fas.harvard.edu.
Harvard University · US

Funding

Human Decidual Lymphocytes and their Placental LigandsR01AI053330 · NIAID · HARVARD UNIVERSITY · PI STROMINGER, JACK L · 2003 to 2014
$4.1M
Human Decidual Leukocytes and Their Placental LigandsR56AI053330 · NIAID · HARVARD UNIVERSITY · PI STROMINGER, JACK L · 2009 to 2009
$415k
NIAID NIH HHS AI053330NIAID NIH HHS R01 AI053330NIAID NIH HHS R56 AI053330
6 · The paper itself

Abstract

The interaction of noncytotoxic decidual natural killer cells (dNK) and extravillous trophoblasts (EVT) at the maternal-fetal interface was studied. Confocal microscopy revealed that many dNK interact with a single large EVT. Filamentous projections from EVT enriched in HLA-G were shown to contact dNK, and may represent the initial stage of synapse formation. As isolated, 2.5% of dNK contained surface HLA-G. However, surface HLA-G-negative dNK contained internalized HLA-G. Activation of dNK resulted in the disappearance of internalized HLA-G in parallel with restoration of cytotoxicity. Surface HLA-G was reacquired by incubation with EVT. This HLA-G cycle of trogocytosis, endocytosis, degradation, and finally reacquisition provides a transient and localized acquisition of new functional properties by dNK upon interaction with EVT. Interruption of the cycle by activation of dNK by cytokines and/or viral products serves to ensure the NK control of virus infection at the interface, and is illustrated here by the response of dNK to human cytomegalo virus (HCMV)-infected decidual stromal cells. Thus, the HLA-G cycle in dNK can provide both for NK tolerance and antiviral immunity.

Indexed as

Blotting, WesternCytokinesCytomegalovirus InfectionsDNA PrimersFemaleFlow CytometryHLA-G AntigensHumansImmune ToleranceKiller Cells, NaturalMaternal-Fetal ExchangeMicroscopy, ConfocalPregnancyReal-Time Polymerase Chain ReactionStatistics, NonparametricTrophoblastsCytokinesDNA PrimersHLA-G AntigenscytotoxicitydeciduaHCMVhumanpregnancy

Identifiers

PMID26460007
PMCPMC4629323
OpenAlexW2201213085

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.