Evidence map›Paper›PMID 25620999›Full record

ArticleFuture virology2014

Novel drugs targeting Toll-like receptors for antiviral therapy.

Mira C Patel, Kari Ann Shirey, Lioubov M Pletneva, Marina S Boukhvalova, Alfredo Garzino-Demo, Stefanie N Vogel, Jorge Cg Blanco

Open access · greenAbstract read
In one paragraph

Article in Future virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

43 citing papers in PubMed, 98 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

7 authors at 2 institutions in 1 country.

Mira C PatelDepartment of Microbiology & Immunology, University of Maryland, School of Medicine, Baltimore, MD 21201, USA.
Kari Ann ShireyDepartment of Microbiology & Immunology, University of Maryland, School of Medicine, Baltimore, MD 21201, USA.
Lioubov M PletnevaSigmovir Biosystems, Inc., Rockville, MD 20850, USA.
Marina S BoukhvalovaSigmovir Biosystems, Inc., Rockville, MD 20850, USA.
Alfredo Garzino-DemoDepartment of Microbiology & Immunology, University of Maryland, School of Medicine, Baltimore, MD 21201, USA ; Institute of Human Virology, University of Maryland, School of Medicine, Baltimore, MD 21201, USA.
Stefanie N VogelDepartment of Microbiology & Immunology, University of Maryland, School of Medicine, Baltimore, MD 21201, USA.
Jorge Cg BlancoSigmovir Biosystems, Inc., Rockville, MD 20850, USA.
University of Maryland, Baltimore · USSigmovir Biosystems (United States) · US

Funding

DIFFERENTIATIVE SIGNALS FOR MACROPHAGE ACTIVATIONR37AI018797 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI VOGEL, STEFANIE N. · 2000 to 2009
$5.3M
The Role of TLR4 and RSV F Protein in Immunity to RSVR01AI057575 · NIAID · VIRION SYSTEMS, INC. · PI BLANCO, JORGE C · 2004 to 2013
$5.1M
DIFFERENTIATIVE SIGNALS FOR MACROPHANGE ACTIVATIONR01AI018797 · NIAID · U.S. UNIFORMED SERVICES UNIV OF HLTH SCI · PI VOGEL, STEFANIE N. · 1985 to 2014
$3.8M
Eritoran (E5564), a TLR4 antagonist, as a novel therapeutic for influenzaR01AI104541 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BLANCO, JORGE C, VOGEL, STEFANIE N. · 2013 to 2016
$3.4M
A Novel Anti-HIV Activity of CCR6 via APOBEC3G: Relevance to CNS InfectionR01NS066842 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI GARZINO-DEMO, ALFREDO · 2009 to 2013
$1.7M
Differentiative Signals for Macrophage ActivationR56AI018797 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI VOGEL, STEFANIE N. · 2015 to 2015
$506k
NIAID NIH HHS R01 AI018797NIAID NIH HHS R01 AI057575NIAID NIH HHS R01 AI104541NIAID NIH HHS R37 AI018797NIAID NIH HHS R56 AI018797NINDS NIH HHS R01 NS066842
6 · The paper itself

Abstract

Toll-like receptors (TLRs) are sentinel receptors of the host innate immune system that recognize conserved 'pathogen-associated molecular patterns' of invading microbes, including viruses. The activation of TLRs establishes antiviral innate immune responses and coordinates the development of long-lasting adaptive immunity in order to control viral pathogenesis. However, microbe-induced damage to host tissues may release 'danger-associated molecular patterns' that also activate TLRs, leading to an overexuberant inflammatory response and, ultimately, to tissue damage. Thus, TLRs have proven to be promising targets as therapeutics for the treatment of viral infections that result in inflammatory damage or as adjuvants in order to enhance the efficacy of vaccines. Here, we explore recent advances in TLR biology with a focus on novel drugs that target TLRs (agonists and antagonists) for antiviral therapy.

Indexed as

antiviral therapyeritoraninnate immune systemmonophosphoryl lipid Apoly-ICLCretrocyclinTLR agonistTLR antagonistToll-like receptorsviruses

Identifiers

PMID25620999
PMCPMC4303062
OpenAlexW1971564068

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.