Evidence map›Paper›PMID 20538505›Full record

ReviewCurrent opinion in microbiology2010

Viral tricks to grid-lock the type I interferon system.

Gijs A Versteeg, Adolfo García-Sastre

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in microbiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 152 papers.

0numbers the graph read from it
0cells of the map it votes in
152citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

152 citing papers in PubMed, 256 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Infection and immunity · 2024
    Article
  6. Review
  7. Article
  8. bioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Regulation of innate immune responses by rabies virus.Animal models and experimental medicine · 2022
    Review
  17. Article
  18. Article
  19. Review
  20. Article

92 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Gijs A VersteegDepartment of Microbiology, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY 10029, USA.
Adolfo García-Sastre
Icahn School of Medicine at Mount Sinai · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LIPKIN, W. IAN · 2003 to 2014
$100.8M
Technological Development ComponentU19AI062623 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI MORAN, THOMAS M · 2004 to 2009
$21.3M
Viral and Host cDNA Libraries from 1918 Influenza CasesP01AI058113 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GARCIA-SASTRE, ADOLFO · 2004 to 2010
$20.3M
TRIM mediated host antiviral responses during influenza virus infectionsU19AI083025 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JUNG, JAE U · 2009 to 2013
$10.0M
Live attenuated vaccines for epidemic and pandemic fluU01AI070469 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GARCIA-SASTRE, ADOLFO · 2006 to 2010
$9.7M
NOVEL CELLULAR AND VIRAL TARGETS FOR ANTI-INFLUENZA VIRUS DRUGSU01AI074539 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI PALESE, PETER · 2007 to 2011
$7.4M
VIRUS INDUCED DC MATURATION AND CELLULAR IMMUNITYP01AI048204 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI PALESE, PETER · 2000 to 2003
$3.8M
VIRULENCE FACTORS OF INFLUENZA VIRUS--THE NS1 PROTEINR01AI046954 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GARCIA-SASTRE, ADOLFO · 2000 to 2010
$3.1M
Functional Analysis of NSV-based HIV vectorsP01AI082325 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SCHNELL, MATTHIAS JOHANNES · 2009 to 2010
$2.7M
NIAID NIH HHS HHSN266200700010CNIAID NIH HHS P01 AI048204NIAID NIH HHS P01 AI058113NIAID NIH HHS P01AI058113NIAID NIH HHS P01 AI082325NIAID NIH HHS P01AI082325NIAID NIH HHS R01 AI046954NIAID NIH HHS R01 AI46954NIAID NIH HHS U01 AI070469NIAID NIH HHS U01AI070469NIAID NIH HHS U01 AI074539NIAID NIH HHS U01AI074539NIAID NIH HHS U19 AI062623NIAID NIH HHS U19 AI083025NIAID NIH HHS U19AI83025NIAID NIH HHS U54 AI057158NIAID NIH HHS U54 AI57158
6 · The paper itself

Abstract

Type I interferons (IFNs) play a crucial role in the innate immune avant-garde against viral infections. Virtually all viruses have developed means to counteract the induction, signaling, or antiviral actions of the IFN circuit. Over 170 different virus-encoded IFN antagonists from 93 distinct viruses have been described up to now, indicating that most viruses interfere with multiple stages of the IFN response. Although every viral IFN antagonist is unique in its own right, four main mechanisms are employed to circumvent innate immune responses: (i) general inhibition of cellular gene expression, (ii) sequestration of molecules in the IFN circuit, (iii) proteolytic cleavage, and (iv) proteasomal degradation of key components of the IFN system. The increasing understanding of how different viral IFN antagonists function has been translated to the generation of viruses with mutant IFN antagonists as potential live vaccine candidates. Moreover, IFN antagonists are attractive targets for inhibition by small-molecule compounds.

Indexed as

AnimalsHumansImmune EvasionInterferon Type IViral VaccinesVirus DiseasesVirusesInterferon Type IViral Vaccines

Identifiers

PMID20538505
PMCPMC2920345
OpenAlexW1964316194

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.