Evidence map›Paper›PMID 25822203›Full record

ArticlePloS one2015

Novel mechanism of arenavirus-induced liver pathology.

Juliane I Beier, Jenny D Jokinen, Gretchen E Holz, Patrick S Whang, Amah M Martin, Nikole L Warner, Gavin E Arteel, Igor S Lukashevich

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 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.6field-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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Juliane I BeierDepartment of Pharmacology and Toxicology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America; Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, Louisville, Kentucky, United States of America.
Jenny D JokinenDepartment of Pharmacology and Toxicology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America; Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, Louisville, Kentucky, United States of America.
Gretchen E HolzDepartment of Pharmacology and Toxicology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America; Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, Louisville, Kentucky, United States of America.
Patrick S WhangDepartment of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America; Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, Louisville, Kentucky, United States of America.
Amah M MartinDepartment of Pharmacology and Toxicology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America.
Nikole L WarnerDepartment of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America; Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, Louisville, Kentucky, United States of America.
Gavin E ArteelDepartment of Pharmacology and Toxicology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America.
Igor S LukashevichDepartment of Pharmacology and Toxicology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky, United States of America; Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, Louisville, Kentucky, United States of America.
University of Louisville · US

Funding

Development of New Bivalent Cross-Protective Arenaviral VaccinesR01AI093450 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI LUKASHEVICH, IGOR S., PUSHKO, PETER M. · 2011 to 2015
$3.9M
Role of ECM and inflammatory remodeling in alcohol-induced liver and lung damage-diversity supplementR01AA021978 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ARTEEL, GAVIN E · 2014 to 2018
$1.8M
NIAAA NIH HHS R01 AA021978NIAAA NIH HHS R01AA021978NIAID NIH HHS R01 AI093450NIAID NIH HHS R01AI093450
6 · The paper itself

Abstract

Viral hemorrhagic fevers (VHFs) encompass a group of diseases with cardinal symptoms of fever, hemorrhage, and shock. The liver is a critical mediator of VHF disease pathogenesis and high levels of ALT/AST transaminases in plasma correlate with poor prognosis. In fact, Lassa Fever (LF), the most prevalent VHF in Africa, was initially clinically described as hepatitis. Previous studies in non-human primate (NHP) models also correlated LF pathogenesis with a robust proliferative response in the liver. The purpose of the current study was to gain insight into the mechanism of liver injury and to determine the potential role of proliferation in LF pathogenesis. C57Bl/6J mice were infected with either the pathogenic (for NHPs) strain of lymphocytic choriomeningitis virus (LCMV, the prototypic arenavirus), LCMV-WE, or with the non-pathogenic strain, LCMV-ARM. As expected, LCMV-WE, but not ARM, caused a hepatitis-like infection. LCMV-WE also induced a robust increase in the number of actively cycling hepatocytes. Despite this increase in proliferation, there was no significant difference in liver size between LCMV-WE and LCMV-ARM, suggesting that cell cycle was incomplete. Indeed, cells appeared arrested in the G1 phase and LCMV-WE infection increased the number of hepatocytes that were simultaneously stained for proliferation and apoptosis. LCMV-WE infection also induced expression of a non-conventional virus receptor, AXL-1, from the TAM (TYRO3/AXL/MERTK) family of receptor tyrosine kinases and this expression correlated with proliferation. Taken together, these results shed new light on the mechanism of liver involvement in VHF pathogenesis. Specifically, it is hypothesized that the induction of hepatocyte proliferation contributes to expansion of the infection to parenchymal cells. Elevated levels of plasma transaminases are likely explained, at least in part, by abortive cell cycle arrest induced by the infection. These results may lead to the development of new therapies to prevent VHF progression.

Indexed as

AnimalsCell CycleCell ProliferationChlorocebus aethiopsCytokinesFemaleLiver DiseasesLymphocytic choriomeningitis virusMiceMice, Inbred C57BLOxidative StressReceptors, VirusStem CellsUp-RegulationVero CellsVirus InternalizationCytokinesReceptors, Virus

Identifiers

PMID25822203
PMCPMC4378851
OpenAlexW2036799271

What OpenQuestion holds

Textmetadata
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.