Evidence map›Paper›PMID 30249022›Full record

ArticleInternational journal of molecular sciences2018

Immunological Heterogeneity of Healthy Peripheral Blood Stem Cell Donors-Effects of Granulocyte Colony-Stimulating Factor on Inflammatory Responses.

Tor Henrik Anderson Tvedt, Guro K Melve, Galina Tsykunova, Aymen Bushra Ahmed, Annette K Brenner, Øystein Bruserud

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. IL-1/MyD88-Dependent G-CSF and IL-6 Secretion Mediates Postburn Anemia.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Observational
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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

6 authors at 1 institution in 1 country.

Tor Henrik Anderson TvedtDepartment of Medicine, Section for Hematology, Haukeland University Hospital, 5021 Bergen, Norway. thetve@helse-bergen.no.
Guro K MelveInstitute of Clinical Science, Section for Hematology, University of Bergen, 5021 Bergen, Norway. guro.kristin.melve@helse-bergen.no.
Galina TsykunovaDepartment of Medicine, Section for Hematology, Haukeland University Hospital, 5021 Bergen, Norway. glts@helse-bergen.no.
Aymen Bushra AhmedDepartment of Medicine, Section for Hematology, Haukeland University Hospital, 5021 Bergen, Norway. abah@helse-bergen.no.
Annette K BrennerDepartment of Medicine, Section for Hematology, Haukeland University Hospital, 5021 Bergen, Norway. Annette.Brenner@uib.no.
Øystein BruserudDepartment of Medicine, Section for Hematology, Haukeland University Hospital, 5021 Bergen, Norway. brus@helse-bergen.no.
Haukeland University Hospital · NO

Funding

Eivind Møllbach Pedersens Foundation N/AHelse Vest 911946Helse Vest 912051Helse Vest 912178Kreftforeningen 100933Kreftforeningen 182609The Blix Family Foundation N/AUniversitetet i Bergen N/A
6 · The paper itself

Abstract

Interleukin-6 (IL-6) contributes to the development of immune-mediated complications after allogeneic stem cell transplantation. However, systemic IL-6 levels also increase during granulocyte colony-stimulating factor (G-CSF) mobilization of hematopoietic stem cells in healthy donors, but it is not known whether this mobilization alters systemic levels of other IL-6 family cytokines/receptors and whether such effects differ between donors. We examined how G-CSF administration influenced C-reactive protein (CRP) levels (85 donors) and serum levels of IL-6 family cytokines/receptors (20 donors). G-CSF increased CRP levels especially in elderly donors with high pretherapy levels, but these preharvesting levels did not influence clinical outcomes (nonrelapse mortality, graft versus host disease). The increased IL-6 levels during G-CSF therapy normalized within 24 h after treatment. G-CSF administration did not alter serum levels of other IL-6-familly mediators. Oncostatin M, but not IL-6, showed a significant correlation with CRP levels during G-CSF therapy. Clustering analysis of mediator levels during G-CSF administration identified two donor subsets mainly characterized by high oncostatin M and IL-6 levels, respectively. Finally, G-CSF could increase IL-6 release by in vitro cultured monocytes, fibroblasts, and mesenchymal stem cells. In summary, G-CSF seems to induce an acute phase reaction with increased systemic IL-6 levels in healthy stem cell donors.

Indexed as

Blood DonorsAdolescentAdultAgedCells, CulturedCytokinesFemaleFibroblastsGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHumansInflammationInflammation MediatorsMiddle AgedMonocytesPeripheral Blood Stem CellsCytokinesGranulocyte Colony-Stimulating FactorInflammation Mediatorsacute-phase reactionC-reactive proteingraft versus host diseaseInterleukin-6tissue and organ procurementtoll-like receptors

Identifiers

PMID30249022
PMCPMC6213426
OpenAlexW2891953766

What OpenQuestion holds

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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.