Evidence map›Paper›PMID 24610880›Full record

ArticleJournal of leukocyte biology2014

Mast cell histamine promotes the immunoregulatory activity of myeloid-derived suppressor cells.

Rebecca K Martin, Sheinei J Saleem, Lauren Folgosa, Hannah B Zellner, Sheela R Damle, Giang-Kim T Nguyen, John J Ryan, Harry D Bear, Anne-Marie Irani, Daniel H Conrad

Abstract read
In one paragraph

Article in Journal of leukocyte biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Pathophysiological role of histamine signaling and its implications in glioblastoma.Biochimica et biophysica acta. Reviews on cancer · 2024
    Review
  6. Review
  7. Article
  8. Review
  9. Here, There, and Everywhere: Myeloid-Derived Suppressor Cells in Immunology.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
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  19. Review
  20. Mast Cell Biology at Molecular Level: a Comprehensive Review.Clinical reviews in allergy & immunology · 2020
    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

10 authors at 1 institution in 1 country.

Rebecca K MartinDepartments of Microbiology and Immunology.
Sheinei J SaleemDepartments of Microbiology and Immunology.
Lauren FolgosaDepartments of Microbiology and Immunology, Center for Clinical and Translational Research;
Hannah B ZellnerDepartments of Microbiology and Immunology.
Sheela R DamleDepartments of Microbiology and Immunology.
Giang-Kim T NguyenDepartments of Microbiology and Immunology.
John J RyanDepartments of Microbiology and Immunology, Biology, and.
Harry D BearDepartments of Microbiology and Immunology, Massey Cancer Center; and Division of Surgical Oncology, Department of Surgery, Virginia Commonwealth University, Richmond, Virginia, USA.
Anne-Marie IraniPediatric Allergy and Immunology;
Daniel H ConradDepartments of Microbiology and Immunology, dconrad@vcu.edu.
Virginia Commonwealth University · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Keri R Maher · 1985 to 2026
$51.0M
The Effect of Lyn Deficiency on Mast Cell Activation and Inflammatory Disease ProU19AI077435 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI CONRAD, DANIEL H · 2008 to 2012
$7.7M
Virginia Commonwealth University IRADCAK12GM093857 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DANIEL C BULLARD, John J Ryan · 2010 to 2026
$7.0M
STRUCTURE/FUNCTION OF THE LYMPHOCYTE FCE RECEPTORR01AI018697 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI MARTIN, REBECCA KELLEY · 1985 to 2018
$6.5M
IL-10 Regulates Mast Cell Function and SurvivalR01AI059638 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI RYAN, JOHN J · 2007 to 2017
$3.8M
Control of IgG-mediated Inflammation by Fyn and Lyn KinasesR01AI101153 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI RYAN, JOHN J · 2013 to 2017
$2.0M
A10Tg mice, a model of MDSC development and function in a tumor free environmentF31CA159877 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SALEEM, SHEINEI JAMAL · 2011 to 2012
$66k
NCI NIH HHS F31 CA159877NCI NIH HHS F31CA159877NCI NIH HHS P30 CA016059NCI NIH HHS P30 CA16059NIAID NIH HHS R01 AI018697NIAID NIH HHS R01 AI059638NIAID NIH HHS R01 AI101153NIAID NIH HHS R01AI18697NIAID NIH HHS U19 AI077435NIAID NIH HHS U19AI077435NIGMS NIH HHS K12 GM093857
6 · The paper itself

Abstract

It has been shown recently that MCs are required for differential regulation of the immune response by granulocytic versus monocytic MDSCs. Granulocytic MDSCs promoted parasite clearance, whereas monocytic MDSCs enhanced tumor progression; both activities were abrogated in MC-deficient mice. Herein, we demonstrate that the lack of MCs also influences MDSC trafficking. Preferential trafficking to the liver was not seen in MC-deficient mice. In addition, evidence that the MC mediator histamine was important in MDSC trafficking and activation is also shown. MDSCs express HR1-3. Blockade of these receptors by HR1 or HR2 antagonists reversed the histamine enhancement of MDSC survival and proliferation observed in cell culture. In addition, histamine differentially influenced Arg1 and iNOS gene expression in MDSCs and greatly enhanced IL-4 and IL-13 message, especially in granulocytic MDSCs. Evidence that histamine influenced activity seen in vitro translated to in vivo when HR1 and HR2 antagonists blocked the effect of MDSCs on parasite expulsion and tumor metastasis. All of these data support the MDSC-mediated promotion of Th2 immunity, leading to the suggestion that allergic-prone individuals would have elevated MDSC levels. This was directly demonstrated by looking at the relative MDSC levels in allergic versus control patients. Monocytic MDSCs trended higher, whereas granulocytic MDSCs were increased significantly in allergic patients. Taken together, our studies indicate that MCs and MC-released histamine are critical for MDSC-mediated immune regulation, and this interaction should be taken into consideration for therapeutic interventions that target MDSCs.

Indexed as

AnimalsCell ProliferationCell SurvivalHistamineHistamine AntagonistsInterleukin-13Interleukin-4Mast CellsMiceMice, Mutant StrainsReceptors, HistamineTh2 CellsHistamineHistamine AntagonistsInterleukin-13Interleukin-4Receptors, Histamineallergic diseasecetirizinecimetidineNippostrongylus brasiliensisparasiteTh2

Identifiers

PMID24610880
PMCPMC4056279
OpenAlexW2047104532

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.