Evidence map›Paper›PMID 27389933›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2016

Percentage of Peripheral CD19+CD24hiCD38hi Regulatory B Cells in Neonatal Sepsis Patients and Its Functional Implication.

Xiao Pan, Zuoquan Ji, Jiang Xue

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
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  7. CD19BMC immunology · 2022
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  8. Review
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  14. Review
  15. Unique aspects of the perinatal immune system.Nature reviews. Immunology · 2017
    Review
  16. Clinical significance of Vδ1 T cell detection in sepsis patients.International journal of clinical and experimental pathology · 2017
    Article
  17. Article
  18. Article
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

3 authors at 3 institutions in 1 country.

Xiao PanDepartment of Internal Medicine, Second Ward, Linyi City People's Hospital, Linyi, Shandong, China (mainland).
Zuoquan JiDepartment of Neonatal, Affiliated Hospital of Shandong Medical College, Linyi, Shandong, China (mainland).
Jiang XueDepartment of Neonatal, Second Hospital of Shandong University, Jinan, Shandong, China (mainland).
Linyi People's Hospital · CNSecond Hospital of Shandong University · CNShandong First Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND As a major cause of mortality in neonates, neonatal sepsis is often accompanied by immune dysfunctions, which are frequently caused by dysregulated T cell sub-populations. The role of regulatory B cells in neonatal sepsis, however, remains unknown. Therefore, this study investigated the percentage and functional variation of CD19+CD24hiCD38hi regulatory B cells in peripheral blood of neonatal sepsis patients in an attempt to elucidate the role of these regulatory B cells in pathogenesis of sepsis. MATERIAL AND METHODS Flow cytometry was used to quantify the percentage of CD19+CD24hiCD38hi regulatory B cells from peripheral blood samples. The correlation between B cell percentage and C reactive protein (CRP) level was analyzed. Secretion level of interleukin-10 (IL-10) and effects on the proliferation of naïve CD4+ T cells were further analyzed. RESULTS The percentage of CD19+CD24hiCD38hi regulatory B cells in neonatal sepsis patients was significantly higher compared to healthy controls (p<0.05), and was positively correlated with serum CRP level. The percentage of IL-10+ CD19+CD24hiCD38hi regulatory B cells was also higher in sepsis patients, and also had more potent inhibition on naïve CD4+ T cells (p<0.01). CONCLUSIONS The elevation of CD19+CD24hiCD38hi regulatory B cells in neonatal sepsis can inhibit body immune function and thus may participate in the pathogenesis of sepsis.

Indexed as

ADP-ribosyl Cyclase 1Antigens, CD19B-Lymphocytes, RegulatoryCD24 AntigenC-Reactive ProteinFemaleFlow CytometryHumansInfantInfant, NewbornInterleukin-10MaleMembrane GlycoproteinsNeonatal SepsisStaphylococcal InfectionsThrombocytopeniaADP-ribosyl Cyclase 1Antigens, CD19CD19 molecule, humanCD24 AntigenCD24 protein, humanCD38 protein, humanC-Reactive ProteinIL10 protein, humanInterleukin-10Membrane Glycoproteins

Identifiers

PMID27389933
PMCPMC4946390
OpenAlexW2472250321

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.