Evidence map›Paper›PMID 42348490›Full record

Trial reportJournal of innate immunity2026

In vivo Cytokine Adsorption Reveals Distinct Neutrophil Mobilization Pathways during Experimental Human Endotoxemia.

Suzanne H Bongers, Bernard N Jukema, Aron Jansen, Dirk van Lier, Nicole Waalders, Matthijs Kox, Peter Pickkers, Loek P H Leenen, Falco Hietbrink, Leo Koenderman and 1 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of innate immunity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Suzanne H BongersDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
Bernard N JukemaCenter for Translational Immunology (CTI), University Medical Center Utrecht, Utrecht, The Netherlands.
Aron JansenDepartment of Intensive Care Medicine, Radboud university medical center, Nijmegen, The Netherlands.
Dirk van LierDepartment of Intensive Care Medicine, Radboud university medical center, Nijmegen, The Netherlands.
Nicole WaaldersDepartment of Intensive Care Medicine, Radboud university medical center, Nijmegen, The Netherlands.
Matthijs KoxDepartment of Intensive Care Medicine, Radboud university medical center, Nijmegen, The Netherlands.
Peter PickkersDepartment of Intensive Care Medicine, Radboud university medical center, Nijmegen, The Netherlands.
Loek P H LeenenDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
Falco HietbrinkDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
Leo KoendermanCenter for Translational Immunology (CTI), University Medical Center Utrecht, Utrecht, The Netherlands.
Nienke VrisekoopCenter for Translational Immunology (CTI), University Medical Center Utrecht, Utrecht, The Netherlands, n.vrisekoop@umcutrecht.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDuring acute inflammation, such as experimental human endotoxemia, circulating neutrophil counts initially decrease, followed by pronounced neutrophilia. Banded (CD16dim/CD62Lbright) and hypersegmented (CD16bright/CD62Ldim) neutrophils, which are absent in the blood during homeostasis, are rapidly mobilized. Banded and mature neutrophils are thought to be recruited from the bone marrow, while the origin of hypersegmented neutrophils remains disputed and underlying recruitment mechanisms remain to be established.

methodsFifteen volunteers received an intravenous bolus of bacterial lipopolysaccharide (LPS) followed by continuous infusion for 3 h. Seven were randomly assigned to additional cytokine adsorption therapy, enabling analysis of neutrophil subsets across a broad range of circulating cytokine concentrations. Blood samples were obtained at baseline and 3 h post-LPS bolus to assess neutrophil subset quantities, neutrophil surface activation markers, and plasma cytokine levels.

resultsCirculating concentrations of pro-inflammatory cytokines (TNF, interleukin (IL)-6, CXCL8, CCL3, and CCL2) were negatively associated with circulating mature and banded neutrophil numbers, suggesting a role for these cytokines in their migration. The absence of a correlation between plasma cytokines with hypersegmented neutrophils indicates an alternative mobilization signal. In contrast to cell numbers, neutrophil activation markers positively correlated with concentrations of the various pro-inflammatory cytokines, indicating involvement of cytokines in neutrophil activation.

conclusionCirculating cytokines appear to be key drivers of mature and banded neutrophil migration, whereas this complex signal does not influence the abundance of CD62Ldim cells in peripheral blood.

Indexed as

CytokinesEndotoxemiaNeutrophilsAdsorptionAdultCell MovementFemaleHumansLipopolysaccharidesMaleNeutrophil ActivationYoung AdultCytokinesLipopolysaccharidesCytokineEndotoxemiaMobilizationNeutrophilSubset

Identifiers

PMID42348490
PMCPMC13485298

What Socratic holds

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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 Socratic graph.