Evidence map›Paper›PMID 24711621›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Gr-1dimCD11b+ immature myeloid-derived suppressor cells but not neutrophils are markers of lethal tuberculosis infection in mice.

Evgeny N Tsiganov, Elena M Verbina, Tatiana V Radaeva, Vasily V Sosunov, George A Kosmiadi, Irina Yu Nikitina, Irina V Lyadova

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

74 citing papers in PubMed, 112 citations in OpenAlex.

  1. Article
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  4. Article
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  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Nutrients · 2023
    Article
  14. Review
  15. Article
  16. Suppressive myeloid cells in SARS-CoV-2 andFrontiers in immunology · 2023
    Article
  17. Immunometabolism of Myeloid-Derived Suppressor Cells: Implications forInternational journal of molecular sciences · 2022
    Review
  18. Article
  19. Article
  20. Exploring the Role of Low-Density Neutrophils DuringFrontiers in cellular and infection microbiology · 2022
    Review

14 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

7 authors at 1 institution in 1 country.

Evgeny N TsiganovDepartment of Immunology, Central Tuberculosis Research Institute, Russian Academy of Medical Sciences, Moscow 107564, Russia.
Elena M Verbina
Tatiana V Radaeva
Vasily V Sosunov
George A Kosmiadi
Irina Yu Nikitina
Irina V Lyadova
Central Scientific Research Institute of Tuberculosis Russian Academy of Medical Sciences · RU

Funding

Cellular and molecular pathways of tuberculosis progressionR01AI078899 · NIAID · CENTRAL INSTITUTE FOR TUBERCULOSIS · PI LYADOVA, IRINA V · 2009 to 2012
$427k
NIAID NIH HHS R01 AI078899PHS HHS AIR01078899
6 · The paper itself

Abstract

Tuberculosis (TB) disease may progress at different rates and have different outcomes. Neutrophils have been implicated in TB progression; however, data on their role during TB are controversial. In this study, we show that in mice, TB progression is associated with the accumulation of cells that express neutrophilic markers Gr-1 and Ly-6G but do not belong to conventional neutrophils. The cells exhibit unsegmented nuclei, have Gr-1(dim)Ly-6G(dim)CD11b(+) phenotype, and express F4/80, CD49d, Ly-6C, CD117, and CD135 markers characteristic not of neutrophils but of immature myeloid cells. The cells accumulate in the lungs, bone marrow, spleen, and blood at the advanced (prelethal) stage of Mycobacterium tuberculosis infection and represent a heterogeneous population of myeloid cells at different stages of their differentiation. The accumulation of Gr-1(dim)CD11b(+) cells is accompanied by the disappearance of conventional neutrophils (Gr-1(hi)Ly-6G(hi)-expressing cells). The Gr-1(dim)CD11b(+) cells suppress T cell proliferation and IFN-γ production in vitro via NO-dependent mechanisms, that is, they exhibit characteristics of myeloid-derived suppressor cells. These results document the generation of myeloid-derived suppressor cells during TB, suggesting their role in TB pathogenesis, and arguing that neutrophils do not contribute to TB pathology at the advanced disease stage.

Indexed as

AnimalsCD11b AntigenCell ProliferationFemaleMiceMycobacterium tuberculosisMyeloid CellsNeutrophilsNitric OxideReceptors, ChemokineT-LymphocytesTuberculosisCD11b AntigenGr-1 protein, mouseNitric OxideReceptors, Chemokine

Identifiers

PMID24711621
PMCPMC4537794
OpenAlexW1491146431

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.