Evidence map›Paper›PMID 21091716›Full record

ReviewAnnals of the New York Academy of Sciences2011

Neurokinin-1 receptor: functional significance in the immune system in reference to selected infections and inflammation.

Steven D Douglas, Susan E Leeman

Abstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

107 citing papers in PubMed, 194 citations in OpenAlex.

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47 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

2 authors at 2 institutions in 1 country.

Steven D DouglasDepartment of Pediatrics, Children's Hospital of Philadelphia Research Institute, University of Pennsylvania Medical School, Philadelphia, Pennsylvania, USA. DOUGLAS@email.chop.edu
Susan E Leeman
Boston University · USChildren's Hospital of Philadelphia · US

Funding

Substance P and NK1R Antagonists in Simian AIDSP01MH076388 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI DOUGLAS, STEVEN DANIEL · 2005 to 2008
$6.5M
TACHYKININS, MONONUCLEAR PHAGOCYTES, AND HIV1 INFECTIONR01MH049981 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI DOUGLAS, STEVEN DANIEL · 1995 to 2012
$5.8M
Project 5U01MH090325 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI BARRETT, JEFFREY SCOTT · 2009 to 2013
$5.6M
NIMH NIH HHS P01 MH076388NIMH NIH HHS P01-MH-076388NIMH NIH HHS R01 MH049981NIMH NIH HHS R01-MH-049981NIMH NIH HHS U01 MH090325NIMH NIH HHS U01-MH-090325
6 · The paper itself

Abstract

The G protein-coupled receptor (GPCR), neurokinin-1 receptor (NK1R), and its preferred ligand, substance P (SP), are reviewed in relationship to the immune system and selected infections. NK1R and SP are ubiquitous throughout the animal kingdom. This important pathway has unique functions in numerous cells and tissues. The interaction of SP with its preferred receptor, NK1R, leads to the activation of nuclear factor-kappa B (NF-κB) and proinflammatory cytokines. NK1R has two isoforms, both a full-length and a truncated form. These isoforms have different functional significances and differ in cell signaling capability. The proinflammatory signals modulated by SP are important in bacterial, viral, fungal, and parasitic diseases, as well as in immune system function. The SP-NK1R system is a major class 1, rhodopsin-like GPCR ligand-receptor interaction.

Indexed as

InfectionsAmino Acid SequenceAnimalsHumansInflammationInflammation MediatorsMolecular Sequence DataProtein IsoformsReceptors, Neurokinin-1Substance PInflammation MediatorsProtein IsoformsReceptors, Neurokinin-1Substance P

Identifiers

PMID21091716
PMCPMC3058850
OpenAlexW1599368877

What OpenQuestion holds

Textmetadata
LicenceTDM
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.