Evidence map›Paper›PMID 23678166›Full record

ArticleJournal of virology2013

Induction of dendritic cell production of type I and type III interferons by wild-type and vaccine strains of measles virus: role of defective interfering RNAs.

Rupak Shivakoti, Martina Siwek, Debra Hauer, Kimberly L W Schultz, Diane E Griffin

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. A Virus Is a Community: Diversity within Negative-Sense RNA Virus Populations.Microbiology and molecular biology reviews : MMBR · 2022
    Review
  4. Article
  5. Article
  6. Inhibition of Nipah Virus by Defective Interfering Particles.The Journal of infectious diseases · 2020
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Measles Vaccine.Viral immunology · 2018
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Limited in vivo production of type I or type III interferon after infection of macaques with vaccine or wild-type strains of measles virus.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2015
    Article
  18. Article
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.

Rupak ShivakotiW. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Martina Siwek
Debra Hauer
Kimberly L W Schultz
Diane E Griffin
Johns Hopkins University · US

Funding

Training: Molecular & Cellular Bases of Infectious DiseasesT32AI007417 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Arturo Casadevall · 1994 to 2026
$11.9M
Immune Responses During Measles Virus InfectionR01AI023047 · NIAID · JOHNS HOPKINS UNIVERSITY · PI GRIFFIN, DIANE E · 1986 to 2007
$2.1M
NIAID NIH HHS R01 AI023047NIAID NIH HHS R01 AI23047NIAID NIH HHS T32 AI007417NIAID NIH HHS T32 AI07417
6 · The paper itself

Abstract

The innate immune response to viral infection frequently includes induction of type I interferons (IFN), but many viruses have evolved ways to block this response and increase virulence. In vitro studies of IFN production after infection of susceptible cells with measles virus (MeV) have often reported greater IFN synthesis after infection with vaccine than with wild-type strains of MeV. However, the possible presence in laboratory virus stocks of 5' copy-back defective interfering (DI) RNAs that induce IFN independent of the standard virus has frequently confounded interpretation of data from these studies. To further investigate MeV strain-dependent differences in IFN induction and the role of DI RNAs, monocyte-derived dendritic cells (moDCs) were infected with the wild-type Bilthoven strain and the vaccine Edmonston-Zagreb strain with and without DI RNAs. Production of type I IFN, type III IFN, and the interferon-stimulated genes (ISGs) Mx and ISG56 by infected cells was assessed with a flow cytometry-based IFN bioassay, quantitative reverse transcriptase PCR (RT-PCR), and immunoassays. Bilthoven infected moDCs less efficiently than Edmonston-Zagreb. Presence of DI RNAs in vaccine stocks resulted in greater maturation of moDCs, inhibition of virus replication, and induction of higher levels of IFN and ISGs. Production of type I IFN, type III IFN, and ISG mRNA and protein was determined by both the level of infection and the presence of DI RNAs. At the same levels of infection and in the absence of DI RNA, IFN induction was similar between wild-type and vaccine strains of MeV.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBase SequenceCell LineChlorocebus aethiopsCricetinaeDefective VirusesDendritic CellsDNA PrimersFlow CytometryHumansImmunity, InnateImmunoblottingInterferonsMeasles virusMolecular Sequence DataAdaptor Proteins, Signal TransducingDNA PrimersIFIT1 protein, humanInterferonsRNA-Binding ProteinsRNA, ViralTranscription FactorsViral Vaccines

Identifiers

PMID23678166
PMCPMC3700182
OpenAlexW2158470747

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.