Evidence map›Paper›PMID 33671836›Full record

ArticleInternational journal of molecular sciences2021

Secreted Ligands of the NK Cell Receptor NKp30: B7-H6 Is in Contrast to BAG6 Only Marginally Released via Extracellular Vesicles.

Viviane Ponath, Nathalie Hoffmann, Leonie Bergmann, Christina Mäder, Bilal Alashkar Alhamwe, Christian Preußer, Elke Pogge von Strandmann

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Viviane PonathInstitute for Tumor Immunology, Clinic for Hematology, Immunology and Oncology, Philipps University of Marburg, Hans-Meerwein-Strasse 3, 35043 Marburg, Germany.
Nathalie HoffmannInstitute for Tumor Immunology, Clinic for Hematology, Immunology and Oncology, Philipps University of Marburg, Hans-Meerwein-Strasse 3, 35043 Marburg, Germany.
Leonie BergmannInstitute for Tumor Immunology, Clinic for Hematology, Immunology and Oncology, Philipps University of Marburg, Hans-Meerwein-Strasse 3, 35043 Marburg, Germany.
Christina MäderInstitute for Tumor Immunology, Clinic for Hematology, Immunology and Oncology, Philipps University of Marburg, Hans-Meerwein-Strasse 3, 35043 Marburg, Germany.
Bilal Alashkar AlhamweInstitute for Tumor Immunology, Clinic for Hematology, Immunology and Oncology, Philipps University of Marburg, Hans-Meerwein-Strasse 3, 35043 Marburg, Germany.ORCID 0000-0002-7120-0013
Christian PreußerInstitute for Tumor Immunology, Clinic for Hematology, Immunology and Oncology, Philipps University of Marburg, Hans-Meerwein-Strasse 3, 35043 Marburg, Germany.
Elke Pogge von StrandmannInstitute for Tumor Immunology, Clinic for Hematology, Immunology and Oncology, Philipps University of Marburg, Hans-Meerwein-Strasse 3, 35043 Marburg, Germany.
Philipps University of Marburg · DE

Funding

Wilhelm Sander-Stiftung 2015.145.1
6 · The paper itself

Abstract

NKp30 (Natural Cytotoxicity Receptor 1, NCR1) is a powerful cytotoxicity receptor expressed on natural killer (NK) cells which is involved in tumor cell killing and the regulation of antitumor immune responses. Ligands for NKp30, including BAG6 and B7-H6, are upregulated in virus-infected and tumor cells but rarely detectable on healthy cells. These ligands are released by tumor cells as part of the cellular secretome and interfere with NK cell activity. BAG6 is secreted via the exosomal pathway, and BAG6-positive extracellular vesicles (EV-BAG6) trigger NK cell cytotoxicity and cytokine release, whereas the soluble protein diminishes NK cell activity. However, the extracellular format and activity of B7-H6 remain elusive. Here, we used HEK293 as a model cell line to produce recombinant ligands and to study their impact on NK cell activity. Using this system, we demonstrate that soluble B7-H6 (sB7-H6), like soluble BAG6 (sBAG6), inhibits NK cell-mediated target cell killing. This was associated with a diminished cell surface expression of NKG2D and NCRs (NKp30, NKp40, and NKp46). Strikingly, a reduced

Indexed as

B7 AntigensExtracellular VesiclesHEK293 CellsHumansIntegrin beta1K562 CellsKiller Cells, NaturalLigandsMolecular ChaperonesNatural Cytotoxicity Triggering Receptor 3Recombinant ProteinsTumor EscapeB7 AntigensBAG6 protein, humanIntegrin beta1Itgb1 protein, humanLigandsMolecular ChaperonesNatural Cytotoxicity Triggering Receptor 3NCR3LG1 protein, humanNCR3 protein, humanRecombinant ProteinsB7-H6BAG6extracellular ligandsNKp30tumor cell killing

Identifiers

PMID33671836
PMCPMC7926927
OpenAlexW3129898554

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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.