Evidence map›Paper›PMID 21927676›Full record

ReviewViruses2011

Intracellular events and cell fate in filovirus infection.

Judith Olejnik, Elena Ryabchikova, Ronald B Corley, Elke Mühlberger

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

47 citing papers in PubMed, 87 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

4 authors at 2 institutions in 2 countries.

Judith OlejnikDepartment of Microbiology, School of Medicine, Boston University, Boston, MA 02118, USA. jolejnik@bu.edu
Elena Ryabchikova
Ronald B Corley
Elke Mühlberger
Boston University · USInstitute of Chemical Biology and Fundamental Medicine · RU

Funding

Treatments for Nipah Virus InfectionU54AI057159 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI CUNNINGHAM, JAMES · 2003 to 2013
$113.7M
Early Host Immune Response in Protection Against Filovirus InfectionU01AI082954 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MUHLBERGER, ELKE C · 2009 to 2013
$3.3M
NIAID NIH HHS AI057159NIAID NIH HHS U01 AI082954NIAID NIH HHS U01-AI082954NIAID NIH HHS U54 AI057159
6 · The paper itself

Abstract

Marburg and Ebola viruses cause a severe hemorrhagic disease in humans with high fatality rates. Early target cells of filoviruses are monocytes, macrophages, and dendritic cells. The infection spreads to the liver, spleen and later other organs by blood and lymph flow. A hallmark of filovirus infection is the depletion of non-infected lymphocytes; however, the molecular mechanisms leading to the observed bystander lymphocyte apoptosis are poorly understood. Also, there is limited knowledge about the fate of infected cells in filovirus disease. In this review we will explore what is known about the intracellular events leading to virus amplification and cell damage in filovirus infection. Furthermore, we will discuss how cellular dysfunction and cell death may correlate with disease pathogenesis.

Indexed as

Genome, ViralAnimalsCell DeathCytopathogenic Effect, ViralDendritic CellsFiloviridaeFiloviridae InfectionsHost-Pathogen InteractionsInclusion Bodies, ViralMacrophagesMicroscopy, Electron, TransmissionRNA, ViralViral ProteinsVirus CultivationVirus InternalizationVirus ReleaseRNA, ViralViral Proteinsanimal modelsbystander apoptosiscell deathEbola VirusfilovirusesMarburg Virustarget cellsultrastructural analysisviral replication cyclevirus-cell interaction

Identifiers

PMID21927676
PMCPMC3172725
OpenAlexW1977240303

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.