Evidence map›Paper›PMID 26241657›Full record

ArticlePloS one2015

NKP30-B7-H6 Interaction Aggravates Hepatocyte Damage through Up-Regulation of Interleukin-32 Expression in Hepatitis B Virus-Related Acute-On-Chronic Liver Failure.

Yong Zou, Junjie Bao, Xingfei Pan, Ying Lu, Sihong Liao, Xicheng Wang, Guoying Wang, Dongjun Lin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. Review
  6. Article
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  9. Article
  10. Review
  11. Article
  12. [Damage-associated molecular patterns and liver failure].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2016
    Review
  13. Natural Killer Cells and Liver Fibrosis.Frontiers in immunology · 2016
    Review
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

8 authors at 5 institutions in 1 country.

Yong ZouDepartment of Blood Transfusion, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Junjie BaoPreterm Birth Prevention and Treatment Research Unit, Department of Obstetrics, Guangzhou Women and Children's Medical Center, Guangzhou, China.
Xingfei PanDepartment of infectious disease, the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Ying LuDepartment of Blood Transfusion, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Sihong LiaoDepartment of Blood Transfusion, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Xicheng WangDepartment of oncology, Zhangqiu People's Hospital, Jinan, China.
Guoying WangDepartment of Liver Transplantation Center, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Dongjun LinDepartment of Blood Transfusion, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China; Department of Hematology, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Third Affiliated Hospital of Sun Yat-sen University · CNGuangzhou Medical University · CNSun Yat-sen University · CNThird Affiliated Hospital of Guangzhou Medical University · CNZhangqiu City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsPrevious work conducted by our group has shown that the accumulation of hepatic natural killer (NK) cells and the up-regulation of natural cytotoxicity receptors (NKP30 and NKP46) on NK cells from patients with hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF) were correlated with disease progression in HBV-ACLF. The natural cytotoxicity receptors expressed on NK cells are believed to be probable candidates involved in the NK cell-mediated hepatocyte damage in HBV-ACLF. However, the underlying mechanisms remain to be elucidated. In the present study, we aimed to discover the role of NKP30-B7-H6 interaction in NK cells-mediated hepatocyte damage in HBV-ACLF.

methodsHepatic expressions of B7-H6 and interleukin-32 (IL-32) were examined by immunochemistry staining in samples from patients with HBV-ACLF or mild chronic hepatitis B (CHB). The cytotoxicity of NK-92 cell against target cells (Huh-7 and LO2) was evaluated by CCK8 assay. Expression of IL-32 in liver NK cell, T cells and NK-92 cell line was detected by the flow cytometric analysis. The effect of IL-32 on the apoptosis of Huh7 cells was evaluated using Annexin V/PI staining analysis.

resultsAn enhancement of hepatic B7-H6 and IL-32 expression was associated with the severity of liver injury in HBV-ACLF. And there was a positive association between hepatic B7-H6 and IL-32 expression. Expressions of IL-32 in liver NK cells and T cells were increased in HBV-ACLF patients. In vitro NK-92 cells are highly capable of killing the high B7-H6 expressing Huh7 cells and B7-H6-tansfected hepatocyte line LO2 cells dependent on NKP30 and B7-H6 interaction. Furthermore, NK-92 cells exhibited elevated IL-32 expression when stimulated with anti-NKP30 antibodies or when co-cultured with Huh7 cells. IL-32 can induce the apoptosis of Huh7 cells in a dose-dependent manner.

conclusionOur results suggest that NKP30-B7-H6 interaction can aggravate hepatocyte damage, probably through up-regulation of IL-32 expression in HBV-ACLF.

Indexed as

Acute-On-Chronic Liver FailureAdultApoptosisB7 AntigensCell Line, TumorFemaleHepatitis BHepatocytesHumansInterleukinsKiller Cells, NaturalLiverMaleMiddle AgedNatural Cytotoxicity Triggering Receptor 3Up-RegulationB7 AntigensIL32 protein, humanInterleukinsNatural Cytotoxicity Triggering Receptor 3NCR3LG1 protein, humanNCR3 protein, human

Identifiers

PMID26241657
PMCPMC4524618
OpenAlexW2191468418

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.