Evidence map›Paper›PMID 30824730›Full record

Observational studyScientific reports2019

Mobilization of Stem and Progenitor Cells in Septic Shock Patients.

Tomasz Skirecki, Małgorzata Mikaszewska-Sokolewicz, Marlena Godlewska, Barbara Dołęgowska, Jarosław Czubak, Grażyna Hoser, Jerzy Kawiak, Urszula Zielińska-Borkowska

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

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  8. Bone marrow vasculature advancedFrontiers in cardiovascular medicine · 2023
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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

8 authors at 4 institutions in 1 country.

Tomasz SkireckiDepartment of Anesthesiology and Intensive Care Medicine, Centre of Postgraduate Medical Education, Marymoncka 99/103, 01-813, Warsaw, Poland. tskirecki@cmkp.edu.pl.ORCID 0000-0001-6233-7758
Małgorzata Mikaszewska-SokolewiczThe 1st Clinic of Anesthesiology and Intensive Care Medicine, Medical University of Warsaw, Lindelya 4, 00-001, Warsaw, Poland.
Marlena GodlewskaDepartment Biochemistry and Molecular Biology, Centre of Postgraduate Medical Education, Marymoncka 99/103, 01-813, Warsaw, Poland.
Barbara DołęgowskaDepartment of Laboratory Medicine, Pomeranian Medical University, Powstańców Wlkp. 72, 70-111, Szczecin, Poland.
Jarosław CzubakDepartment of Pediatric Orthopedics, Centre of Postgraduate Medical Education, Marymoncka 99/103, 01-813, Warsaw, Poland.
Grażyna HoserLaboratory of Flow Cytometry, Centre of Postgraduate Medical Education, Marymoncka 99/103, 01-813, Warsaw, Poland.
Jerzy KawiakNalecz Institute of Biocybernetics and Biomedical Engineering, PAS, Trojdena 4, 02-109, Warsaw, Poland.
Urszula Zielińska-BorkowskaDepartment of Anesthesiology and Intensive Care Medicine, Centre of Postgraduate Medical Education, Marymoncka 99/103, 01-813, Warsaw, Poland.
Postgraduate School of Molecular Medicine · PLInstitute of Biocybernetics and Biomedical Engineering · PLMedical University of Warsaw · PLPomeranian Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Septic shock is associated with multiple injuries to organs and tissues. These events may induce the regenerative response of adult stem cells. However, little is known about how endogenous stem cells are modulated by sepsis. This study analyzed the circulation of hematopoietic stem cells (HSCs), endothelial progenitor cells (EPCs) and very small embryonic-like stem cells (VSELs) in the peripheral blood of patients with septic shock. Thirty-three patients with septic shock and twenty-two healthy control subjects were enrolled in this prospective observational study. Blood samples were collected on the first, third and seventh days of septic shock. Populations of stem cells were analyzed by flow cytometry. Chemotactic mediators were analyzed by HPLC and ELISA. Populations of early HSCs (Lin-CD133+CD45+ and CD34+CD38-) were mobilized to the peripheral blood after an initial decrease. Mobilized HSCs showed significantly increased expression of Ki-67, a marker of cell proliferation. Circulating EPCs and VSELs were mobilized to the blood circulation upon the first day of sepsis. Patients with a greater number of Lin-CD133+CD45+ HSCs and Lin-CD34+CD45- VSELs had a significantly lower probability of 60-day survival. The concentration of CXCL12 was elevated in the blood of septic patients, while the concentration of sphingosine-1-phosphate was significantly decreased. As an emergency early response to sepsis, VSELs and EPCs were mobilized to the peripheral blood, while the HSCs showed delayed mobilization. Differential mobilization of stem cell subsets reflected changes in the concentration of chemoattractants in the blood. The relationship between the probability of death and a large number of HSCs and VSELs in septic shock patients can be used as a novel prognostic marker and may provide new therapeutic approaches.

Indexed as

Antigens, CDChemokine CXCL12Endothelial Progenitor CellsHematopoietic Stem CellsShock, SepticAgedBiomarkersFemaleHumansMaleMiddle AgedProspective StudiesAntigens, CDBiomarkersChemokine CXCL12CXCL12 protein, human

Identifiers

PMID30824730
PMCPMC6397313
OpenAlexW2916757157

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.