Evidence map›Paper›PMID 30575728›Full record

ArticleNature communications2018

A virus-encoded type I interferon decoy receptor enables evasion of host immunity through cell-surface binding.

Bruno Hernáez, Juan Manuel Alonso-Lobo, Imma Montanuy, Cornelius Fischer, Sascha Sauer, Luis Sigal, Noemí Sevilla, Antonio Alcamí

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. A comprehensive overview of monkeypox virus disease.Tropical medicine and health · 2026
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  12. Comprehensive literature review of monkeypox.Emerging microbes & infections · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
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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 6 institutions in 3 countries.

Bruno HernáezCentro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas (CSIC)-Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
Juan Manuel Alonso-LoboCentro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas (CSIC)-Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
Imma MontanuyCentro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas (CSIC)-Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
Cornelius FischerMax Planck Institute for Molecular Genetics, 14195, Berlin, Germany.
Sascha SauerMax Planck Institute for Molecular Genetics, 14195, Berlin, Germany.
Luis SigalDepartment of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA, 19107, USA.
Noemí SevillaCentro de Investigación en Sanidad Animal; Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, 28130, Valdeolmos, Madrid, Spain.
Antonio AlcamíCentro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas (CSIC)-Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain. aalcami@cbm.csic.es.
Centro de Biología Molecular Severo Ochoa · ESMax Planck Institute for Molecular Genetics · DEConsejo Superior de Investigaciones Científicas · ESInstituto Nacional de Investigación y Tecnología Agraria y Alimentaria · ESThomas Jefferson University · USUniversidad Autónoma de Madrid · ES

Funding

Orthropoxvirus Pathogenesis and VaccinesR01AI065544 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2006 to 2016
$5.7M
Inflammatory monocytes in the draining lymph node of ECTV infected miceR01AI110457 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SIGAL, LUIS J · 2015 to 2019
$2.3M
NIAID NIH HHS R01 AI065544NIAID NIH HHS R01 AI110457
6 · The paper itself

Abstract

Soluble cytokine decoy receptors are potent immune modulatory reagents with therapeutic applications. Some virus-encoded secreted cytokine receptors interact with glycosaminoglycans expressed at the cell surface, but the biological significance of this activity in vivo is poorly understood. Here, we show the type I interferon binding protein (IFNα/βBP) encoded by vaccinia and ectromelia viruses requires of this cell binding activity to confer full virulence to these viruses and to retain immunomodulatory activity. Expression of a variant form of the IFNα/βBP that inhibits IFN activity, but does not interact with cell surface glycosaminoglycans, results in highly attenuated viruses with a virulence similar to that of the IFNα/βBP deletion mutant viruses. Transcriptomics analysis and infection of IFN receptor-deficient mice confirmed that the control of IFN activity is the main function of the IFNα/βBP in vivo. We propose that retention of secreted cytokine receptors at the cell surface may largely enhance their immunomodulatory activity.

Indexed as

AnimalsChlorocebus aethiopsFemaleGlycosaminoglycansHeLa CellsHumansInterferon Type IMiceMice, Inbred BALB CPoxviridaePoxviridae InfectionsVero CellsViral ProteinsVirus AttachmentGlycosaminoglycansInterferon Type IViral Proteins

Identifiers

PMID30575728
PMCPMC6303335
OpenAlexW2905103427

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.