Evidence map›Paper›PMID 25029205›Full record

ArticleJournal of the American Chemical Society2014

Stimulation of innate immune cells by light-activated TLR7/8 agonists.

Keun Ah Ryu, Lalisa Stutts, Janine K Tom, Rock J Mancini, Aaron P Esser-Kahn

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 56 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Keun Ah RyuDepartment of Chemistry, University of California , Irvine, California 92697, United States.
Lalisa Stutts
Janine K Tom
Rock J Mancini
Aaron P Esser-Kahn
University of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
Directing The Immune System Via Polymeric Combinations of Molecular SignalsDP2AI112194 · NIAID · UNIVERSITY OF CHICAGO · PI ESSER-KAHN, AARON P · 2013 to 2013
$2.3M
NCI NIH HHS P30 CA062203NIAID NIH HHS DP2 AI112194NIAID NIH HHS DP2-AI112194
6 · The paper itself

Abstract

The innate immune response is controlled, in part, by the synergistic interaction of multiple Toll-like receptors (TLRs). This multi-receptor cooperation is responsible for the potent activity of many vaccines, but few tools have been developed to understand the spatio-temporal elements of TLR synergies. In this Communication, we present photo-controlled agonists of TLR7/8. By strategically protecting the active agonist moiety based on an agonist-bound crystal structure, TLR activity is suppressed and then regained upon exposure to light. We confirmed NF-κB production upon light exposure in a model macrophage cell line. Primary cell activity was confirmed by examining cytokine and cell surface marker production in bone-marrow-derived dendritic cells. Finally, we used light to activate dendritic cell sub-populations within a larger population.

Indexed as

LightAminoquinolinesAnimalsBone Marrow CellsCell LineDendritic CellsImiquimodImmunity, InnateMiceModels, MolecularProtein MultimerizationProtein Structure, QuaternaryToll-Like Receptor 7Toll-Like Receptor 8AminoquinolinesImiquimodToll-Like Receptor 7Toll-Like Receptor 8

Identifiers

PMID25029205
PMCPMC4132957
OpenAlexW2321719622

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.