Evidence map›Paper›PMID 29288958›Full record

ArticleVirology2018

Inhibition of type I interferon responses by adenovirus serotype-dependent Gas6 binding.

Natalie F Nidetz, Tom M Gallagher, Christopher M Wiethoff

Abstract read
In one paragraph

Article in Virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. mInternational journal of molecular sciences · 2022
    Article
  8. Review
  9. Article
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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

3 authors at 1 institution in 1 country.

Natalie F NidetzLoyola University Chicago, 2016 S. First Avenue, Maywood, IL 60153, USA. Electronic address: nnidetz@luc.edu.
Tom M GallagherLoyola University Chicago, 2016 S. First Avenue, Maywood, IL 60153, USA. Electronic address: tgallag@luc.edu.
Christopher M WiethoffLoyola University Chicago, 2016 S. First Avenue, Maywood, IL 60153, USA. Electronic address: cwiethoff@lilly.com.
Loyola University Chicago · US

Funding

Experimental Immunology Training GrantT32AI007508 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KNIGHT, KATHERINE L. · 1997 to 2022
$4.0M
NIAID NIH HHS T32 AI007508
6 · The paper itself

Abstract

The clinical use of many adenovirus vaccine vectors (AdVs) is limited by the presence of pre-existing antibodies in human populations, which prevent common AdVs from transducing cells and expressing immunogenic gene products. Rare serotype AdVs, such as HAdV-28D can bypass pre-existing immunity. However, rare AdVs stimulate high-levels of type I interferon (IFN), which suppresses antigenic gene expression and therefore limits immunogenicity. Recent studies identified Gas6 as a factor that connects enveloped viruses to host-cell receptor tyrosine kinases, in turn generating signaling cascades that antagonize type I IFN responses. We discovered that Gas6 bound to the fiber proteins of common AdV serotypes, such as HAdV-5C, with a higher affinity than rare HAd-28D fibers. AdV-associated Gas6 suppressed IFN production by common AdVs and enhanced long-term expression of AdV encoded genes. We hypothesize that rare AdV serotypes might be engineered to include Gas6 binding motifs, thereby generating novel vectors that are more effective.

Indexed as

AdenoviridaeAdenoviridae InfectionsCapsid ProteinsGrowth Arrest-Specific Protein 6Host-Pathogen InteractionsHumansIntercellular Signaling Peptides and ProteinsInterferon-betaProtein BindingSerogroupCapsid ProteinsGrowth Arrest-Specific Protein 6hexon capsid protein, AdenovirusIntercellular Signaling Peptides and ProteinsInterferon-betaAdenovirusGas6Gene therapyInnate immunityTAM receptorsType I interferonsVaccine vectors

Identifiers

PMID29288958
PMCPMC6110086
OpenAlexW2779692667

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.