Evidence map›Paper›PMID 25615700›Full record

ReviewCurrent opinion in immunology2015

Microbial strategies for antagonizing Toll-like-receptor signal transduction.

Charles V Rosadini, Jonathan C Kagan

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Inhibitory Role of anFrontiers in microbiology · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. TheThe Journal of biological chemistry · 2017
    Article
  15. Article
  16. AThe EMBO journal · 2017
    Article
  17. Article
  18. Review
  19. Article
  20. Early innate immune responses to bacterial LPS.Current opinion in immunology · 2017
    Review
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

2 authors at 2 institutions in 1 country.

Charles V RosadiniHarvard Medical School and Division of Gastroenterology, Boston Children's Hospital, Boston, MA 02115, USA.
Jonathan C KaganHarvard Medical School and Division of Gastroenterology, Boston Children's Hospital, Boston, MA 02115, USA. Electronic address: jonathan.kagan@childrens.harvard.edu.
Boston Children's Hospital · USHarvard University · US

Funding

STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WAYNE I LENCER · 1986 to 2026
$32.4M
Initiation and Regulation of Antiviral Innate ImmunityR01AI093589 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI KAGAN, JONATHAN C · 2011 to 2020
$4.4M
Initiation and Regulation of Antiviral Innate ImmunityR56AI093589 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI KAGAN, JONATHAN C · 2021 to 2021
$531k
Cellular and molecular aspects of Toll-like receptor signal transduction.R00AI072955 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI KAGAN, JONATHAN C · 2008 to 2009
$498k
Initiation and regulation of antibacterial innate immunityR56AI113141 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI KAGAN, JONATHAN C · 2014 to 2014
$456k
Defining non-transcriptional innate immune responses to bacterial endotoxinR56AI103082 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI KAGAN, JONATHAN C · 2013 to 2013
$411k
Regulation of Innate Immunity in Intestinal Epithelial CellsF32DK102317 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI ROSADINI, CHARLES VICTOR · 2014 to 2015
$109k
Cellular and molecular aspects of Toll-like receptor signal transduction.K99AI072955 · NIAID · YALE UNIVERSITY · PI KAGAN, JONATHAN C · 2007 to 2007
$90k
NIAID NIH HHS AI072955NIAID NIH HHS AI093589NIAID NIH HHS K99 AI072955NIAID NIH HHS R00 AI072955NIAID NIH HHS R01 AI093589NIAID NIH HHS R56 AI093589NIAID NIH HHS R56 AI103082NIAID NIH HHS R56 AI113141NIDDK NIH HHS DK102317-01NIDDK NIH HHS F32 DK102317NIDDK NIH HHS P30 DK034854NIDDK NIH HHS P30 DK34854
6 · The paper itself

Abstract

Within a few years of the discovery of Toll-like receptors (TLRs) and their role in innate immunity, viral and bacterial proteins were recognized to antagonize TLR signal transduction. Since then, as TLR signaling networks were unraveled, microbial systems have been discovered that target nearly every component within these pathways. However, recent findings as well as some notable exceptions promote the idea that more of these systems have yet to be discovered. For example, we know very little about microbial systems for directly targeting non-cytoplasmic portions of TLR signaling pathways, that is, the ligand interacting portions of the receptor itself. In this review, we compare and contrast strategies by which bacteria and viruses antagonize TLR signaling networks to identify potential areas for future research.

Indexed as

Microbiological PhenomenaSignal TransductionAnimalsHumansIntracellular Signaling Peptides and ProteinsMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMitogen-Activated Protein KinasesMultiprotein ComplexesProtein BindingTNF Receptor-Associated Factor 6Toll-Like ReceptorsTranscription FactorsIntracellular Signaling Peptides and ProteinsMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMitogen-Activated Protein KinasesMultiprotein ComplexesTNF Receptor-Associated Factor 6Toll-Like ReceptorsTranscription Factors

Identifiers

PMID25615700
PMCPMC4336813
OpenAlexW2162991051

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.