Evidence map›Paper›PMID 35758160›Full record

ArticleEMBO reports2022

Engagement of TRAIL triggers degranulation and IFNγ production in human natural killer cells.

Johannes Höfle, Timo Trenkner, Nadja Kleist, Vera Schwane, Sarah Vollmers, Bryan Barcelona, Annika Niehrs, Pia Fittje, Van Hung Huynh-Tran, Jürgen Sauter and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

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  9. HCMV-secreted glycoprotein gpUL4 inhibits TRAIL-mediated apoptosis and NK cell activation.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

16 authors at 4 institutions in 2 countries.

Johannes Höfle *Leibniz Institute of Virology, Hamburg, Germany.ORCID 0000-0003-4791-3379
Timo Trenkner *Leibniz Institute of Virology, Hamburg, Germany.ORCID 0000-0001-8276-9398
Nadja Kleist *Leibniz Institute of Virology, Hamburg, Germany.ORCID 0000-0002-0409-0467
Vera SchwaneLeibniz Institute of Virology, Hamburg, Germany.
Sarah VollmersLeibniz Institute of Virology, Hamburg, Germany.
Bryan BarcelonaLeibniz Institute of Virology, Hamburg, Germany.ORCID 0000-0002-7726-1052
Annika NiehrsLeibniz Institute of Virology, Hamburg, Germany.ORCID 0000-0002-2190-4346
Pia FittjeLeibniz Institute of Virology, Hamburg, Germany.ORCID 0000-0002-0123-9844
Van Hung Huynh-TranInserm, Bordeaux Population Health Research Center, UMR1219 and Inria, team SISTM, University of Bordeaux, Bordeaux, France.
Jürgen SauterDKMS, Tübingen, Germany.ORCID 0000-0001-8485-2945
Alexander H SchmidtDKMS, Tübingen, Germany.ORCID 0000-0003-0979-5914
Sven PeineInstitute of Transfusion Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Angelique HoelzemerLeibniz Institute of Virology, Hamburg, Germany.
Laura RichertInserm, Bordeaux Population Health Research Center, UMR1219 and Inria, team SISTM, University of Bordeaux, Bordeaux, France.ORCID 0000-0002-7682-2225
Marcus AltfeldLeibniz Institute of Virology, Hamburg, Germany.ORCID 0000-0001-5972-2997
Christian KörnerLeibniz Institute of Virology, Hamburg, Germany.ORCID 0000-0002-3431-7319
Leibniz Institute of Virology (LIV) · DEDeutsche Knochenmarkspenderdatei · DEUniversité de Bordeaux · FRUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NK cells utilize a large array of receptors to screen their surroundings for aberrant or virus-infected cells. Given the vast diversity of receptors expressed on NK cells we seek to identify receptors involved in the recognition of HIV-1-infected cells. By combining an unbiased large-scale screening approach with a functional assay, we identify TRAIL to be associated with NK cell degranulation against HIV-1-infected target cells. Further investigating the underlying mechanisms, we demonstrate that TRAIL is able to elicit multiple effector functions in human NK cells independent of receptor-mediated induction of apoptosis. Direct engagement of TRAIL not only results in degranulation but also IFNγ production. Moreover, TRAIL-mediated NK cell activation is not limited to its cognate death receptors but also decoy receptor I, adding a new perspective to the perceived regulatory role of decoy receptors in TRAIL-mediated cytotoxicity. Based on these findings, we propose that TRAIL not only contributes to the anti-HIV-1 activity of NK cells but also possesses a multifunctional role beyond receptor-mediated induction of apoptosis, acting as a regulator for the induction of different effector functions.

Indexed as

Cytotoxicity, ImmunologicHIV-1HumansInterferon-gammaKiller Cells, NaturalLymphocyte ActivationTNF-Related Apoptosis-Inducing LigandInterferon-gammaTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humandeath receptordegranulationHIV-1NK cellTRAIL

Identifiers

PMID35758160
PMCPMC9346491
OpenAlexW4283639996

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.