Evidence map›Paper›PMID 24636146›Full record

ReviewMolecular immunology2015

Mast cell mediator responses and their suppression by pathogenic and commensal microorganisms.

Hae Woong Choi, Soman N Abraham

Open access · greenAbstract readReview
In one paragraph

Review in Molecular immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Mast Cell Biology at Molecular Level: a Comprehensive Review.Clinical reviews in allergy & immunology · 2020
    Review
  3. Mast cells are critical for controlling the bacterial burden and the healing of infected wounds.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  4. Future Needs in Mast Cell Biology.International journal of molecular sciences · 2019
    Review
  5. Article
  6. Article
  7. Article
  8. 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 2 countries.

Hae Woong ChoiDepartment of Pathology, Duke University Medical Center, Durham, NC 27710, USA.
Soman N AbrahamDepartment of Pathology, Duke University Medical Center, Durham, NC 27710, USA; Department of Immunology, Duke University Medical Center, Durham, NC 27710, USA; Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA; Program in Emerging Infectious Diseases, Duke-National University of Singapore, Singapore 169857, Singapore. Electronic address: soman.abraham@duke.edu.
Duke Medical Center · USNational University of Singapore · SG

Funding

Development of Efficacious and Stable Nasal Vaccine FormulationsU01AI082107 · NIAID · DUKE UNIVERSITY · PI STAATS, HERMAN F · 2009 to 2013
$3.8M
Overcoming Immunosenescence by Nanoparticle-Mediated ActivationR01AI096305 · NIAID · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N, LEONG, KAM W · 2012 to 2016
$1.8M
Mast Cells in Dengue Pathology and PreventionR01HL112921 · NHLBI · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 2013 to 2016
$1.5M
Immune mediated exocytosis of intravesicular UPEC from bladder cellsR01DK101456 · NIDDK · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 2014 to 2017
$1.4M
Mechanism of Bacterial Expulsion from Infected Bladder Cells.R56DK095198 · NIDDK · DUKE UNIVERSITY · PI ABRAHAM, SOMAN N · 2012 to 2012
$200k
NHLBI NIH HHS R01 HL112921NIAID NIH HHS R01 AI096305NIAID NIH HHS R01-AI096305NIAID NIH HHS U01 AI082107NIAID NIH HHS U01-AI082107NIDDK NIH HHS R01 DK101456NIDDK NIH HHS R56 DK095198NIDDK NIH HHS R56-DK095198
6 · The paper itself

Abstract

Mast cells (MCs) are selectively found at the host environment interface and are capable of secreting a wide array of pharmacologically active mediators, many of which are prepackaged in granules. Over the past two decades, it has become clear that these cells have the capacity to recognize a range of infectious agents allowing them to play a key role in initiating and modulating early immune responses to infectious agents. However, a number of pathogenic and commensal microbes appear to have evolved distinct mechanisms to suppress MC mediator release to avoid elimination in the host. Understanding how these microbes suppress MC functions may have significant therapeutic value to relieve inflammatory disorders mediated by MCs.

Indexed as

Antimicrobial Cationic PeptidesBacterial InfectionsCytokinesCytoplasmic GranulesEicosanoidsHistamineHumansImmune EvasionImmunity, InnateMast CellsMycosesAntimicrobial Cationic PeptidesCytokinesEicosanoidsHistamineAnti-inflammatoryCommensalDegranulationInfectionMast cellsMast cell-suppressionPathogen

Identifiers

PMID24636146
PMCPMC4326045
OpenAlexW2036579226

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.