Evidence map›Paper›PMID 29172874›Full record

ArticleInnate immunity2018

Nfia deletion in myeloid cells blocks expansion of myeloid-derived suppressor cells during sepsis.

Jun Dai, Ajinkya Kumbhare, Danielle A Williams, Dima Youssef, Zhi Q Yao, Charles E McCall, Mohamed El Gazzar

Open access · bronzeAbstract read
In one paragraph

Article in Innate immunity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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
  5. Review
  6. Review
  7. Role of miRNA dysregulation in sepsis.Molecular medicine (Cambridge, Mass.) · 2022
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Myeloid-Derived Suppressor Cells in Sepsis.Frontiers in immunology · 2019
    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

7 authors at 2 institutions in 1 country.

Jun Dai1 Department of Internal Medicine, 12324 East Tennessee State University College of Medicine , Johnson City, TN, USA.
Ajinkya Kumbhare1 Department of Internal Medicine, 12324 East Tennessee State University College of Medicine , Johnson City, TN, USA.
Danielle A Williams2 Department of Health Sciences, 144478 East Tennessee State University College of Public Health , Johnson City, TN, USA.
Dima Youssef1 Department of Internal Medicine, 12324 East Tennessee State University College of Medicine , Johnson City, TN, USA.
Zhi Q Yao1 Department of Internal Medicine, 12324 East Tennessee State University College of Medicine , Johnson City, TN, USA.
Charles E McCall3 Department of Internal Medicine, Section of Molecular Medicine, 12279 Wake Forest University School of Medicine , Winston-Salem, NC, USA.
Mohamed El Gazzar1 Department of Internal Medicine, 12324 East Tennessee State University College of Medicine , Johnson City, TN, USA.
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

Sepsis-induced immunosuppression increases the risk of chronic infection and reduces survival. Myeloid-derived suppressor cells (MDSCs) expand in the bone marrow and spleen during murine polymicrobial sepsis, contributing to immunosuppression. A better understanding of molecular controls of MDSC production is needed to identify treatment targets. We previously reported that miR-21 and miR-181b couple with transcription factor NFI-A to induce MDSCs during murine sepsis. Here, we expand upon these observations by showing that conditional deletion of the Nfia gene in the myeloid lineage precludes MDSC development. NFI-A-deficient Gr1

Indexed as

AnimalsCD11b AntigenCD4-Positive T-LymphocytesCell DifferentiationCell LineageDendritic CellsGene DeletionImmune ToleranceMacrophagesMiceMice, Inbred BALB CMice, KnockoutMicroRNAsMyeloid CellsNFI Transcription FactorsSepsisCD11b AntigenMicroRNAsMIRN21 microRNA, mouseNfia protein, mouseNFI Transcription Factorsimmune suppressionmyeloid-derived suppressor cellNFI-ASepsis

Identifiers

PMID29172874
PMCPMC6240914
OpenAlexW2768097210

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.