Evidence map›Paper›PMID 26595890›Full record

ArticleNature immunology2016

An innate antiviral pathway acting before interferons at epithelial surfaces.

Marie B Iversen, Line S Reinert, Martin K Thomsen, Ieva Bagdonaite, Ramya Nandakumar, Natalia Cheshenko, Thaneas Prabakaran, Sergey Y Vakhrushev, Malgosha Krzyzowska, Sine K Kratholm and 12 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 71 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 8 institutions in 6 countries.

Marie B IversenDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.
Line S ReinertDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.
Martin K ThomsenDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.
Ieva BagdonaiteDepartment of Cellular and Molecular Medicine, Centre for Glycomics, University of Copenhagen, Copenhagen, Denmark.
Ramya NandakumarDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.
Natalia CheshenkoDepartment of Pediatrics and Microbiology, Albert Einstein College of Medicine, New York, USA.
Thaneas PrabakaranDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.
Sergey Y VakhrushevDepartment of Cellular and Molecular Medicine, Centre for Glycomics, University of Copenhagen, Copenhagen, Denmark.
Malgosha KrzyzowskaDepartment of Regenerative Medicine, Military Institute of Hygiene and Epidemiology, Warsaw, Poland.
Sine K KratholmDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.
Fernando Ruiz-PerezDepartment of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Steen V PetersenDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.
Stanislas GorielyInstitute for Medical Immunology, Université Libre de Bruxelles, Gosselies, Belgium.
Bo Martin BibbyDepartment of Biostatistics, University of Aarhus, Aarhus, Denmark.
Kristina ErikssonDepartment of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, Sweden.
Jürgen RulandInstitut für Klinische Chemie und Pathobiochemie, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Allan R ThomsenDepartment of Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Betsy C HeroldDepartment of Pediatrics and Microbiology, Albert Einstein College of Medicine, New York, USA.
Hans H WandallDepartment of Cellular and Molecular Medicine, Centre for Glycomics, University of Copenhagen, Copenhagen, Denmark.
Sebastian FrischeDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.ORCID http://orcid.org/0000-0002-0270-3602
Christian K HolmDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.
Søren R PaludanDepartment of Biomedicine, University of Aarhus, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-9180-4060
Aarhus University · DKUniversity of Copenhagen · DKAlbert Einstein College of Medicine · USTUM Klinikum · DEUniversité Libre de Bruxelles · BEUniversity of Gothenburg · SEUniversity of Virginia · USWojskowy Instytut Higieny i Epidemiologii · PL

Funding

NIAID NIH HHS AI065309
6 · The paper itself

Abstract

Mucosal surfaces are exposed to environmental substances and represent a major portal of entry for microorganisms. The innate immune system is responsible for early defense against infections and it is believed that the interferons (IFNs) constitute the first line of defense against viruses. Here we identify an innate antiviral pathway that works at epithelial surfaces before the IFNs. The pathway is activated independently of known innate sensors of viral infections through a mechanism dependent on viral O-linked glycans, which induce CXCR3 chemokines and stimulate antiviral activity in a manner dependent on neutrophils. This study therefore identifies a previously unknown layer of antiviral defense that exerts its action on epithelial surfaces before the classical IFN response is operative.

Indexed as

Immunity, InnateAnimalsCell LineChemokine CXCL10Disease Models, AnimalFemaleGene ExpressionGlycosylationHerpes SimplexHerpesvirus 2, HumanHumansInterferonsLigandsMiceMice, KnockoutMucous MembraneChemokine CXCL10InterferonsLigandsPolysaccharidesReceptors, CXCR3Viral Envelope Proteins

Identifiers

PMID26595890
OpenAlexW2209535043

What OpenQuestion holds

Textmetadata
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.