Evidence map›Paper›PMID 21185371›Full record

ReviewBiochimica et biophysica acta2012

Mast cells and inflammation.

Theoharis C Theoharides, Konstantinos-Dionysios Alysandratos, Asimenia Angelidou, Danae-Anastasia Delivanis, Nikolaos Sismanopoulos, Bodi Zhang, Shahrzad Asadi, Magdalini Vasiadi, Zuyi Weng, Alexandra Miniati and 1 more

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 383 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
383citing papers in PubMed, 4 pooled it
7.7field-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.

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

383 citing papers in PubMed, 4 syntheses or guidelines pooled it, 747 citations in OpenAlex.

  1. Pooled it
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  6. iScience · 2026
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323 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

11 authors at 2 institutions in 2 countries.

Theoharis C TheoharidesLaboratory of Molecular Immunopharmacology and Drug Discovery, Department of Molecular Physiology and Pharmacology, Tufts University School of Medicine, Boston, MA 02111, USA. theoharis.theoharides@tufts.edu
Konstantinos-Dionysios Alysandratos
Asimenia Angelidou
Danae-Anastasia Delivanis
Nikolaos Sismanopoulos
Bodi Zhang
Shahrzad Asadi
Magdalini Vasiadi
Zuyi Weng
Alexandra Miniati
Dimitrios Kalogeromitros
Tufts University · USUniversity General Hospital Attikon · GR

Funding

Stress Induces Skin Mast Cell Activation &VasodilationR01AR047652 · NIAMS · TUFTS UNIVERSITY BOSTON · PI THEOHARIDES, THEOHARIS C. · 2001 to 2011
$3.0M
Role of Neuropeptides in Diabetic Foot ProblemsR01NS066205 · NINDS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI PRADHAN-NABZDYK, LEENA, VEVES, ARISTIDIS · 2010 to 2014
$1.9M
Brain mast cells and Chronic Fatigue SyndromeR01NS071361 · NINDS · TUFTS UNIVERSITY BOSTON · PI THEOHARIDES, THEOHARIS C. · 2010 to 2013
$1.4M
NIAMS NIH HHS AR47652NIAMS NIH HHS R01 AR047652NINDS NIH HHS NS55681NINDS NIH HHS NS66205NINDS NIH HHS NS71361NINDS NIH HHS R01 NS066205NINDS NIH HHS R01 NS071361
6 · The paper itself

Abstract

Mast cells are well known for their role in allergic and anaphylactic reactions, as well as their involvement in acquired and innate immunity. Increasing evidence now implicates mast cells in inflammatory diseases where they are activated by non-allergic triggers, such as neuropeptides and cytokines, often exerting synergistic effects as in the case of IL-33 and neurotensin. Mast cells can also release pro-inflammatory mediators selectively without degranulation. In particular, IL-1 induces selective release of IL-6, while corticotropin-releasing hormone secreted under stress induces the release of vascular endothelial growth factor. Many inflammatory diseases involve mast cells in cross-talk with T cells, such as atopic dermatitis, psoriasis and multiple sclerosis, which all worsen by stress. How mast cell differential responses are regulated is still unresolved. Preliminary evidence suggests that mitochondrial function and dynamics control mast cell degranulation, but not selective release. Recent findings also indicate that mast cells have immunomodulatory properties. Understanding selective release of mediators could explain how mast cells participate in numerous diverse biologic processes, and how they exert both immunostimulatory and immunosuppressive actions. Unraveling selective mast cell secretion could also help develop unique mast cell inhibitors with novel therapeutic applications. This article is part of a Special Issue entitled: Mast cells in inflammation.

Indexed as

AnimalsCorticotropin-Releasing HormoneHumansInflammationInflammation MediatorsMast CellsMultiple SclerosisSkin DiseasesStress, PhysiologicalCorticotropin-Releasing HormoneInflammation Mediators

Identifiers

PMID21185371
PMCPMC3318920
OpenAlexW1979278210

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.