Evidence map›Paper›PMID 19230638›Full record

ReviewCurrent opinion in immunology2009

TREM and TREM-like receptors in inflammation and disease.

Jill W Ford, Daniel W McVicar

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03795285 (The Role of Neutrophil CD64 and Soluble Triggering Receptor Expressed on Myeloid Cells 1 in Neonatal Sepsis), which is not on this map. Cited by 253 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
253citing papers in PubMed, 3 pooled it
7.6field-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.

NCT03795285 unknown statusnot on this mapstarted 2019, after this paper: background citation

The Role of Neutrophil CD64 and Soluble Triggering Receptor Expressed on Myeloid Cells 1 in Neonatal Sepsis

TypeobservationalSponsorAssiut UniversityRan2019 to 2019Enrolled50ConditionsNeonatal SEPSISArmsExpression of neutrophil CD64
3 · Its place in the literature

Who cites it

253 citing papers in PubMed, 3 syntheses or guidelines pooled it, 434 citations in OpenAlex.

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193 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.

Jill W FordCancer and Inflammation Program, National Cancer Institute-Frederick, MD 21702, USA.
Daniel W McVicar
National Cancer Institute · US

Funding

Signal Transduction of Paired Inhibitory Receptors of NK Cells and MacrophagesZIABC010300 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MCVICAR, DANIEL W. · 2009 to 2025
$24.6M
Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

Since the discovery of triggering receptor expressed on myeloid cells (TREM)-1 in 2000, evidence documenting the profound ability of the TREM and TREM-like receptors to regulate inflammation has rapidly accumulated. Monocytes, macrophages, myeloid dendritic cells, plasmacytoid dendritic cells, neutrophils, microglia, osteoclasts, and platelets all express at least one member of the TREM family, underscoring the importance of these proteins in the regulation of innate resistance. Recent work on the TREM family includes: characterization of a new receptor expressed on plasmacytoid dendritic cells; definition of a key role for TREM in inflammatory bowel disease and multiple sclerosis; an expanded list of diseases associated with the release of soluble forms of TREM proteins; and identification of the first well characterized TREM ligand: B7-H3, a ligand for TREM-like Transcript (TLT)-2. Moreover, analysis of TREM signaling has now identified key regulatory components and defined pathways that may be responsible for the complex functional interactions between the TREM and toll-like receptors. In addition, there is expanding evidence of a role for TREM in the regulation of integrin function via Plexin-A1. Together these new findings define the TREM and TREM-like receptors as pluripotent modifiers of disease through the integration of inflammatory signals with those associated with leukocyte adhesion.

Indexed as

AnimalsAntigens, CDAutoimmune DiseasesB7 AntigensBacterial InfectionsCell AdhesionDendritic CellsFeedback, PhysiologicalGene Expression RegulationHumansInflammationMembrane GlycoproteinsOsteogenesisReceptor Cross-TalkReceptors, ImmunologicSignal TransductionAntigens, CDB7 AntigensCD276 protein, humanMembrane GlycoproteinsReceptors, ImmunologicTREM1 protein, humanTREML2 protein, humanTriggering Receptor Expressed on Myeloid Cells-1

Identifiers

PMID19230638
PMCPMC2723941
OpenAlexW2019558661

What OpenQuestion holds

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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.