Evidence map›Paper›PMID 37386090›Full record

ArticleScientific reports2023

The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells.

Meike Kaulfuss, Juliane Mietz, Astrid Fabri, Johannes Vom Berg, Christian Münz, Obinna Chijioke

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

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  16. An appeal for biological variation estimates in deep immunophenotyping.Clinical chemistry and laboratory medicine · 2025
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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

6 authors.

Meike KaulfussCellular Immunotherapy, Institute of Experimental Immunology, University of Zürich, Zurich, Switzerland.
Juliane MietzCellular Immunotherapy, Institute of Experimental Immunology, University of Zürich, Zurich, Switzerland.
Astrid FabriCellular Immunotherapy, Institute of Experimental Immunology, University of Zürich, Zurich, Switzerland.
Johannes Vom BergInstitute of Laboratory Animal Science, University of Zürich, Schlieren, Switzerland.
Christian MünzViral Immunobiology, Institute of Experimental Immunology, University of Zürich, Zurich, Switzerland.
Obinna ChijiokeCellular Immunotherapy, Institute of Experimental Immunology, University of Zürich, Zurich, Switzerland. chijioke@immunology.uzh.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human natural killer (NK) cells are cytotoxic effector cells that are increasingly harnessed in cancer immunotherapy. NKG2A/CD94 is an inhibitory receptor on NK cells that has established regulatory functions in the direct interaction with target cells when engaged with its ligand, the non-classical HLA class I molecule HLA-E. Here, we confirmed NKG2A as a checkpoint molecule in primary human NK cells and identified a novel role for NKG2A in maintaining NK cell expansion capacity by dampening both proliferative activity and excessive activation-induced cell death. Maintenance of NK cell expansion capacity might contribute to the preferential accumulation of human NKG2A

Indexed as

Hematopoietic Stem Cell TransplantationKiller Cells, NaturalCell CycleCell ProliferationErythrocytes, AbnormalHumansNK Cell Lectin-Like Receptor Subfamily CKLRC1 protein, humanNK Cell Lectin-Like Receptor Subfamily C

Identifiers

PMID37386090
PMCPMC10310841

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.