Evidence map›Paper›PMID 27328755›Full record

ArticleScientific reports2016

Attenuated viral hepatitis in Trem1-/- mice is associated with reduced inflammatory activity of neutrophils.

Jan-Hendrik Kozik, Tanja Trautmann, Antonella Carambia, Max Preti, Marc Lütgehetmann, Till Krech, Christiane Wiegard, Joerg Heeren, Johannes Herkel

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. 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
0.6field-weighted citation impact, top 30% 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, 18 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. HIV-1 Tat Upregulates TREM1 Expression in Human Microglia.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Pathogens (Basel, Switzerland) · 2021
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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

9 authors at 2 institutions in 1 country.

Jan-Hendrik KozikUniversity Medical Centre Hamburg-Eppendorf, Department of Medicine I, 20246 Hamburg, Germany.
Tanja TrautmannUniversity Medical Centre Hamburg-Eppendorf, Department of Medicine I, 20246 Hamburg, Germany.
Antonella CarambiaUniversity Medical Centre Hamburg-Eppendorf, Department of Medicine I, 20246 Hamburg, Germany.
Max PretiUniversity Medical Centre Hamburg-Eppendorf, Department of Medicine I, 20246 Hamburg, Germany.
Marc LütgehetmannUniversity Medical Centre Hamburg-Eppendorf, Institute of Medical Microbiology, Virology and Hygiene, 20246 Hamburg, Germany.
Till KrechUniversity Medical Centre Hamburg-Eppendorf, Institute of Pathology, 20246 Hamburg, Germany.
Christiane WiegardUniversity Medical Centre Hamburg-Eppendorf, Department of Medicine I, 20246 Hamburg, Germany.
Joerg HeerenUniversity Medical Centre Hamburg-Eppendorf, Institute of Biochemistry and Molecular Cell Biology, 20246 Hamburg, Germany.
Johannes HerkelUniversity Medical Centre Hamburg-Eppendorf, Department of Medicine I, 20246 Hamburg, Germany.
Universität Hamburg · DEUniversity Medical Center Hamburg-Eppendorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TREM1 (Triggering Receptor Expressed on Myeloid Cells 1) is a pro-inflammatory receptor expressed by phagocytes, which can also be released as a soluble molecule (sTREM1). The roles of TREM1 and sTREM1 in liver infection and inflammation are not clear. Here we show that patients with hepatitis B virus (HBV) or hepatitis C virus (HCV) infection manifest elevated serum levels of sTREM1. In mice, experimental viral hepatitis induced by infection with Lymphocytic Choriomeningitis Virus (LCMV)-WE was likewise associated with increased sTREM1 in serum and urine, and with increased TREM1 and its associated adapter molecule DAP12 in the liver. Trem1-/- mice showed accelerated clearance of LCMV-WE and manifested attenuated liver inflammation and injury. TREM1 expression in the liver of wild-type mice was mostly confined to infiltrating neutrophils, which responded to LCMV by secretion of CCL2 and TNF-α, and release of sTREM1. Accordingly, the production of CCL2 and TNF-α was decreased in the livers of LCMV-infected Trem1-/- mice, as compared to LCMV-infected wildtype mice. These findings indicate that TREM1 plays a role in viral hepatitis, in which it seems to aggravate the immunopathology associated with viral clearance, mainly by increasing the inflammatory activity of neutrophils.

Indexed as

AdultAgedAnimalsArenaviridae InfectionsCase-Control StudiesChemokine CCL2FemaleHepatitis BHepatitis CHepatitis, Viral, AnimalHumansInflammationLiverLymphocytic choriomeningitis virusMaleMiceCcl2 protein, mouseChemokine CCL2TREM1 protein, humanTREM1 protein, mouseTriggering Receptor Expressed on Myeloid Cells-1Tumor Necrosis Factor-alpha

Identifiers

PMID27328755
PMCPMC4916511
OpenAlexW2469418588

What OpenQuestion holds

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LicenceCC BY
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.