Evidence map›Paper›PMID 30467624›Full record

ArticleHepatology international2019

Activity of IL-12/15/18 primed natural killer cells against hepatocellular carcinoma.

Lihui Zhuang, Rebecca J Fulton, Pauline Rettman, A Emre Sayan, Jonathan Coad, Aymen Al-Shamkhani, Salim I Khakoo

Abstract read
In one paragraph

Article in Hepatology international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

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  11. Cell-cell communication: new insights and clinical implications.Signal transduction and targeted therapy · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Harnessing the power of memory-like NK cells to fight cancer.Clinical and experimental immunology · 2023
    Article
  16. Article
  17. Review
  18. Article
  19. Review
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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.

Lihui ZhuangFaculty of Medicine, Southampton General Hospital, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
Rebecca J FultonFaculty of Medicine, Southampton General Hospital, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
Pauline RettmanFaculty of Medicine, Southampton General Hospital, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
A Emre SayanFaculty of Medicine, Southampton General Hospital, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
Jonathan CoadFaculty of Medicine, Southampton General Hospital, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
Aymen Al-ShamkhaniFaculty of Medicine, Southampton General Hospital, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
Salim I KhakooFaculty of Medicine, Southampton General Hospital, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK. s.i.khakoo@soton.ac.uk.ORCID http://orcid.org/0000-0002-4057-9091

Funding

Cancer Research UK 19502Cancer Research UK 19917Cancer Research UK 21621Cancer Research UK 25778Cancer Research UK C11972/A19917Medical Research Council MR/M019829/1
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is common, but remains difficult to treat. Natural killer (NK) cells are cells of the innate immune system that have potent anti-cancer activity. Recent work has shown that stimulation with IL-12/15/18 leads to the generation of NK cells with enhanced functional and putative "memory" properties. We have investigated the activity of these NK cells against HCC cell lines in vitro and in a mouse model.

methodsNK cells from healthy donors or individuals with HCC were activated with IL-12/15/18 in vitro and tested for cytotoxic activity against a panel of human HCC cell lines. IL-12/15/18 primed murine NK cells were then infused into a murine model of spontaneously arising HCC to test for anti-tumor activity.

resultsNK cells from patients and healthy controls had similar expression levels of activating and inhibitory NK cell receptors. However, proliferation of NK cells from HCC patients was weaker than healthy controls in response to IL-12/15/18 and IL-2 (p < 0.001 at day 9). In vitro, NK cells from both groups of individuals killed HCC targets to similar levels and this was unrelated to NKG2D expression. In a spontaneous model of HCC, IL-12/15/18 activated NK cells trafficked to the liver and resulted in lower levels of spontaneous HCC formation (p < 0.01).

conclusionCytokine-primed NK cells from patients with HCC have similar levels of activity against HCC cell lines as those from healthy controls. This type of activated NK cell has immunotherapeutic potential against hepatocellular carcinoma.

Indexed as

AgedAnimalsCarcinoma, HepatocellularCell Line, TumorCytokinesDisease Models, AnimalFemaleHumansImmunity, InnateImmunotherapyInterleukin-12Interleukin-15Interleukin-18Killer Cells, NaturalLiver NeoplasmsMaleCytokinesInterleukin-12Interleukin-15Interleukin-18KLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily KCancerCytokinesImmunotherapyInnate immunityLiver

Identifiers

PMID30467624
PMCPMC6513806

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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.