Evidence map›Paper›PMID 29603284›Full record

ReviewBioEssays : news and reviews in molecular, cellular and developmental biology2018

Demarcation of Viral Shelters Results in Destruction by Membranolytic GTPases: Antiviral Function of Autophagy Proteins and Interferon-Inducible GTPases.

Hailey M Brown, Scott B Biering, Allen Zhu, Jayoung Choi, Seungmin Hwang

Open access · hybridAbstract readReview
In one paragraph

Review in BioEssays : news and reviews in molecular, cellular and developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 8 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

5 authors at 1 institution in 1 country.

Hailey M BrownCommittee on Immunology, The University of Chicago, Chicago, IL, 60637, USA.
Scott B BieringCommittee on Microbiology, The University of Chicago, Chicago, IL, 60637, USA.
Allen ZhuCommittee on Cancer Biology, The University of Chicago, Chicago, IL, 60637, USA.
Jayoung ChoiDepartment of Pathology, The University of Chicago, Chicago, IL, 60637, USA.
Seungmin HwangCommittee on Immunology, The University of Chicago, Chicago, IL, 60637, USA.ORCID 0000-0003-0846-5462
University of Chicago · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI CHIEN-MIN KAO · 1985 to 2026
$122.1M
ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI CHANG, EUGENE B · 1990 to 2025
$29.8M
Molecular And Cellular Biology Training ProgramT32GM007183 · NIGMS · UNIVERSITY OF CHICAGO · PI GLICK, BENJAMIN S, RICE, PHOEBE A · 1985 to 2021
$23.9M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
Novel antiviral activity of interferon-gamma against viral replication complexR01AI127518 · NIAID · UNIVERSITY OF CHICAGO · PI RANDALL, GLENN C · 2017 to 2020
$1.6M
Targeting by autophagy proteins for anti-tumor immunityDP2CA225208 · NCI · UNIVERSITY OF CHICAGO · PI HWANG, SEUNGMIN · 2017 to 2017
$510k
NCATS NIH HHS UL1 TR000430NCI NIH HHS DP2 CA225208NCI NIH HHS P30 CA014599NIAID NIH HHS R01 AI127518NIAID NIH HHS T32 AI007090NIDDK NIH HHS P30 DK042086NIGMS NIH HHS T32 GM007183
6 · The paper itself

Abstract

A hallmark of positive-sense RNA viruses is the formation of membranous shelters for safe replication in the cytoplasm. Once considered invisible to the immune system, these viral shelters are now found to be antagonized through the cooperation of autophagy proteins and anti-microbial GTPases. This coordinated effort of autophagy proteins guiding GTPases functions against not only the shelters of viruses but also cytoplasmic vacuoles containing bacteria or protozoa, suggesting a broad immune-defense mechanism against disparate vacuolar pathogens. Fundamental questions regarding this process remain: how the host recognizes these membranous structures as a target, how the autophagy proteins bring the GTPases to the shelters, and how the recruited GTPases disrupt these shelters. In this review, these questions are discussed, the answers to which will significantly advance our understanding of the response to vacuole-like structures of pathogens, thereby paving the way for the development of broadly effective anti-microbial strategies for public health.

Indexed as

AnimalsAntiviral AgentsAutophagyGTP PhosphohydrolasesHumansInterferonsRNA VirusesVacuolesAntiviral AgentsGTP PhosphohydrolasesInterferonsautophagyinterferon-inducible GTPasesLC3 conjugationpathogen-containing vacuolespositive-sense RNA virusreplication compartmentvacuolar pathogen

Identifiers

PMID29603284
PMCPMC5986617
OpenAlexW2794886375

What OpenQuestion holds

Textmetadata
LicenceTDM
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.