Evidence map›Paper›PMID 22706087›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Cutting edge: mast cells critically augment myeloid-derived suppressor cell activity.

Sheinei J Saleem, Rebecca K Martin, Johanna K Morales, Jamie L Sturgill, David R Gibb, Laura Graham, Harry D Bear, Masoud H Manjili, John J Ryan, Daniel H Conrad

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Here, There, and Everywhere: Myeloid-Derived Suppressor Cells in Immunology.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  11. Schlafen4Frontiers in immunology · 2023
    Article
  12. Review
  13. Review
  14. Review
  15. The correlation between infiltration of FoxP3Central-European journal of immunology · 2022
    Article
  16. Translocation ofOncoimmunology · 2022
    Article
  17. Review
  18. Review
  19. Chemokine-Cytokine Networks in the Head and Neck Tumor Microenvironment.International journal of molecular sciences · 2021
    Review
  20. 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.

Sheinei J SaleemDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Rebecca K Martin
Johanna K Morales
Jamie L Sturgill
David R Gibb
Laura Graham
Harry D Bear
Masoud H Manjili
John J Ryan
Daniel H Conrad
Virginia Commonwealth University · US

Funding

The Effect of Lyn Deficiency on Mast Cell Activation and Inflammatory Disease ProU19AI077435 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI ZHAO, WEI · 2008 to 2012
$7.7M
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 F31CA159877NIAID NIH HHS R01AI19697NIAID NIH HHS U19 AI077435NIAID NIH HHS U19AI077435
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs) are primarily recognized for their immunosuppressive properties in malignant disease. However, their interaction with other innate immune cells and their regulation of immune responses, such as in parasitic infection, necessitate further characterization. We used our previously published mouse model of MDSC accumulation to examine the immunoregulatory role of MDSCs in B16 melanoma metastasis and Nippostrongylus brasiliensis infection. In this study, we demonstrate that the activity of MDSCs is dependent on the immune stimuli and subset induced. Monocytic MDSCs predictably suppressed antitumor immune responses but granulocytic MDSCs surprisingly enhanced the clearance of N. brasiliensis infection. Intriguingly, both results were dependent on MDSC interaction with mast cells (MCs), as demonstrated by adoptive-transfer studies in MC-deficient (Kit(Wsh)(/)(Wsh)) mice. These findings were further supported by ex vivo cocultures of MCs and MDSCs, indicating a synergistic increase in cytokine production. Thus, MCs can enhance both immunosuppressive and immunosupportive functions of MDSCs.

Indexed as

AnimalsCarcinoma, Lewis LungCell CommunicationCell Line, TumorCells, CulturedCoculture TechniquesGranulocytesMast CellsMelanoma, ExperimentalMiceMice, Inbred C57BLMice, Mutant StrainsMice, TransgenicMonocytesMyeloid CellsNippostrongylus

Identifiers

PMID22706087
PMCPMC3392490
OpenAlexW2113340900

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.