Evidence map›Paper›PMID 31484831›Full record

ArticleJCI insight2019

Progranulin prevents regulatory NK cell cytotoxicity against antiviral T cells.

Anfei Huang, Prashant V Shinde, Jun Huang, Tina Senff, Haifeng C Xu, Cassandra Margotta, Dieter Häussinger, Thomas E Willnow, Jinping Zhang, Aleksandra A Pandyra and 4 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  7. Article
  8. Article
  9. Article
  10. Targeting natural killer cells to enhance vaccine responses.Trends in pharmacological sciences · 2021
    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

14 authors at 4 institutions in 2 countries.

Anfei HuangDepartment of Molecular Medicine II and.
Prashant V ShindeDepartment of Molecular Medicine II and.
Jun HuangDepartment of Molecular Medicine II and.
Tina SenffInstitute of Virology, Medical Faculty, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
Haifeng C XuDepartment of Molecular Medicine II and.
Cassandra MargottaDepartment of Molecular Medicine II and.
Dieter HäussingerDepartment of Gastroenterology, Hepatology and Infectious Diseases, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
Thomas E WillnowMolecular Cardiovascular Research, Max-Delbrueck-Center for Molecular Medicine, Berlin, Germany.
Jinping ZhangInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, China.
Aleksandra A PandyraDepartment of Molecular Medicine II and.
Jörg TimmInstitute of Virology, Medical Faculty, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
Sascha WeggenDepartment of Neuropathology, Medical Faculty, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
Karl S LangInstitute of Immunology, Medical Faculty, Universität Duisburg-Essen, Essen, Germany.
Philipp A LangDepartment of Molecular Medicine II and.
Heinrich Heine University Düsseldorf · DEMax Delbrück Center · DESoochow University · CNUniversity of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

`NK cell-mediated regulation of antigen-specific T cells can contribute to and exacerbate chronic viral infection, but the protective mechanisms against NK cell-mediated attack on T cell immunity are poorly understood. Here, we show that progranulin (PGRN) can reduce NK cell cytotoxicity through reduction of NK cell expansion, granzyme B transcription, and NK cell-mediated lysis of target cells. Following infection with the lymphocytic choriomeningitis virus (LCMV), PGRN levels increased - a phenomenon dependent on the presence of macrophages and type I IFN signaling. Absence of PGRN in mice (Grn-/-) resulted in enhanced NK cell activity, increased NK cell-mediated killing of antiviral T cells, reduced antiviral T cell immunity, and increased viral burden, culminating in increased liver immunopathology. Depletion of NK cells restored antiviral immunity and alleviated pathology during infection in Grn-/- mice. In turn, PGRN treatment improved antiviral T cell immunity. Taken together, we identified PGRN as a critical factor capable of reducing NK cell-mediated attack of antiviral T cells.

Indexed as

AnimalsCD8-Positive T-LymphocytesCyclin-Dependent Kinase 9Cyclin TCytotoxicity, ImmunologicDisease Models, AnimalHEK293 CellsHumansKiller Cells, NaturalLiverLymphocyte ActivationLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMacrophagesMiceMice, Inbred C57BLCdk9 protein, mouseCyclin-Dependent Kinase 9Cyclin TProgranulinsAdaptive immunityImmunologyInfectious diseaseInnate immunityNK cells

Identifiers

PMID31484831
PMCPMC6777906
OpenAlexW2971485884

What OpenQuestion holds

Textmetadata
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.