Evidence map›Paper›PMID 19474110›Full record

ReviewPharmacological reviews2009

Therapeutic targeting of Toll-like receptors for infectious and inflammatory diseases and cancer.

Luke A J O'Neill, Clare E Bryant, Sarah L Doyle

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Pharmacological reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02284074 (Nasal Lipopolysaccharide), which is not on this map. Cited by 189 papers.

0numbers the graph read from it
0cells of the map it votes in
189citing papers in PubMed
11.8field-weighted citation impact, top 1% 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.

NCT02284074 nacompletednot on this mapstarted 2010, after this paper: background citation

Nasal Lipopolysaccharide (LPS) Challenge in Healthy Volunteers (HVs): Investigation of Tolerability, Dose Response and the Expression Profile of Intercellular Adhesion Molecule-1 (ICAM-1)

TypeinterventionalSponsorImperial College LondonRan2010 to 2011Enrolled15ConditionsHealthyArmsNasal LPS spray, Experimental: Nasal LPS spray 1µg, Experimental: Nasal LPS spray 10 µg, Experimental: Nasal LPS spray 30 µg, Experimental: Nasal LPS spray 100 µg
3 · Its place in the literature

Who cites it

189 citing papers in PubMed, 421 citations in OpenAlex.

  1. Trial
  2. Observational
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. o-Vanillin binds covalently to MAL/TIRAP Lys-210 but independently inhibits TLR2.Journal of enzyme inhibition and medicinal chemistry · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Frontiers in cellular and infection microbiology · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Review

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

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 2 institutions in 3 countries.

Luke A J O'NeillSchool of Biochemistry and Immunology, Trinity College Dublin, Ireland. laoneill@tcd.ie
Clare E Bryant
Sarah L Doyle
Trinity College Dublin · IEUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/C005503/1Biotechnology and Biological Sciences Research Council BB\C005503\1Wellcome TrustWellcome Trust WT081744MA
6 · The paper itself

Abstract

Since first being described in the fruit fly Drosophila melanogaster, Toll-like receptors (TLRs) have proven to be of great interest to immunologists and investigators interested in the molecular basis to inflammation. They recognize pathogen-derived factors and also products of inflamed tissue, and trigger signaling pathways that lead to activation of transcription factors such as nuclear factor-kappaB and the interferon regulatory factors. These in turn lead to induction of immune and inflammatory genes, including such important cytokines as tumor necrosis factor-alpha and type I interferon. Much evidence points to a role for TLRs in immune and inflammatory diseases and increasingly in cancer. Examples include clear roles for TLR4 in sepsis, rheumatoid arthritis, ischemia/reperfusion injury, and allergy. TLR2 has been implicated in similar pathologic conditions and also in systemic lupus erythematosus (SLE) and tumor metastasis. TLR7 has also been shown to be important in SLE. TLR5 has been shown to be radioprotective. Recent advances in our understanding of signaling pathways activated by TLRs, structural insights into TLRs bound to their ligands and antagonists, and approaches to inhibit TLRs (including antibodies, peptides, and small molecules) are providing possiblemeans by which to interfere with TLRs clinically. Here we review these recent advances and speculate about whether manipulating TLRs is likely to be successful in fighting off different diseases.

Indexed as

AnimalsDrug Delivery SystemsHumansInfectionsInflammation MediatorsNeoplasmsToll-Like ReceptorsInflammation MediatorsToll-Like Receptors

Identifiers

PMID19474110
PMCPMC2846156
OpenAlexW2120211786

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.