Evidence map›Paper›PMID 31078118›Full record

ArticleMolecular immunology2019

S100A9 maintains myeloid-derived suppressor cells in chronic sepsis by inducing miR-21 and miR-181b.

Tuqa Alkhateeb, Ajinkya Kumbhare, Isatou Bah, Dima Youssef, Zhi Q Yao, Charles E McCall, Mohamed El Gazzar

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Molecular immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Myeloid-derived suppressor cells in sepsis: drivers of persistent immunosuppression and targets for precision immunotherapy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Role of miRNA dysregulation in sepsis.Molecular medicine (Cambridge, Mass.) · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. High S100A9Aging · 2021
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Tuqa AlkhateebDepartment of Internal Medicine, East Tennessee State University College of Medicine, Johnson City, TN, United States.
Ajinkya KumbhareDepartment of Internal Medicine, East Tennessee State University College of Medicine, Johnson City, TN, United States.
Isatou BahDepartment of Internal Medicine, East Tennessee State University College of Medicine, Johnson City, TN, United States.
Dima YoussefDepartment of Internal Medicine, East Tennessee State University College of Medicine, Johnson City, TN, United States.
Zhi Q YaoDepartment of Internal Medicine, East Tennessee State University College of Medicine, Johnson City, TN, United States.
Charles E McCallDepartment of Internal Medicine, Section of Molecular Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Mohamed El GazzarDepartment of Internal Medicine, East Tennessee State University College of Medicine, Johnson City, TN, United States. Electronic address: elgazzar@etsu.edu.
East Tennessee State University · USWake Forest University · US

Funding

MicroRNAs and myeloid cell development during sepsisR01GM103887 · NIGMS · EAST TENNESSEE STATE UNIVERSITY · PI ELGAZZAR, MOHAMED A. · 2013 to 2018
$1.4M
NIGMS NIH HHS R01 GM103887
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSC) expand during sepsis, suppress both innate and adaptive immunity, and promote chronic immunosuppression, which characterizes the late/chronic phase of sepsis. We previously reported that the transcription factors Stat3 and C/EBPβ synergize to induces the expression of microRNA (miR)-21 and miR-181b to promote MDSC expansion in a mouse model of polymicrobial sepsis that progresses from an early/acute proinflammatory phase to a late/chronic immunosuppressive stage. We also showed that Gr1

Indexed as

AnimalsAntigens, LyCalgranulin BCCAAT-Enhancer-Binding Protein-betaCD11b AntigenDisease Models, AnimalImmunosuppression TherapyInflammationInterleukin-10MaleMiceMice, Inbred C57BLMice, KnockoutMicroRNAsMyeloid CellsMyeloid-Derived Suppressor CellsAntigens, LyCalgranulin BCCAAT-Enhancer-Binding Protein-betaCD11b AntigenInterleukin-10MicroRNAsmirn181 microRNA, mouseMIRN21 microRNA, mouseS100A9 protein, mouseSTAT3 Transcription FactorImmune suppressionMDSCS100A9Sepsis

Identifiers

PMID31078118
PMCPMC6646085
OpenAlexW2944391397

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.