Evidence map›Paper›PMID 40386776›Full record

ArticleFrontiers in immunology2025

Dynamics of neutrophil phenotype and function in sickle cell disease.

Aafke E Gaartman, Lydian A de Ligt, Boukje M Beuger, Anton T J Tool, Martijn Veldthuis, Taco W Kuijpers, Rob van Zwieten, Bart J Biemond, Robin van Bruggen, Erfan Nur

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Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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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

10 authors.

Aafke E GaartmanDepartment of Hematology, Amsterdam University Medical Center, Amsterdam, Netherlands.
Lydian A de LigtDepartment of Hematology, Amsterdam University Medical Center, Amsterdam, Netherlands.
Boukje M BeugerRed Cell Laboratory, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
Anton T J ToolRed Cell Laboratory, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
Martijn VeldthuisLaboratory of Red Blood Cell Diagnostics and Iron, Sanquin Diagnostics, Amsterdam, Netherlands.
Taco W KuijpersRed Cell Laboratory, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
Rob van ZwietenLaboratory of Red Blood Cell Diagnostics and Iron, Sanquin Diagnostics, Amsterdam, Netherlands.
Bart J BiemondDepartment of Hematology, Amsterdam University Medical Center, Amsterdam, Netherlands.
Robin van Bruggen *Red Cell Laboratory, Sanquin Research and Landsteiner Laboratory, Amsterdam, Netherlands.
Erfan Nur *Department of Hematology, Amsterdam University Medical Center, Amsterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: While sickle cell disease (SCD) is primarily acknowledged as an erythrocyte disorder, emerging evidence suggests a role for altered neutrophil phenotype and function in SCD pathophysiology and disease severity. Given the conflicting findings in previous studies, we performed a comprehensive exploration of neutrophil characteristics in SCD patients during steady state and vaso-occlusive crisis (VOC), as well as in response to therapeutic interventions. Methods: Neutrophil phenotype was assessed by flow cytometry and functional properties were evaluated by measurement of neutrophil adhesion and reactive oxygen species (ROS) production. Results: A total of 49 SCD patients (of whom 19 during both steady state and VOC) along with 16 healthy ethnicity-matched and 30 non-matched controls, were included in the study. Differences were observed between neutrophils from patients compared to controls and between control groups. Neutrophil phenotype was more activated in SCD patients compared to non-matched controls. Neutrophil adhesion was increased in steady-state SCD patients compared to both ethnicity-matched and non-matched controls. Discussion: While neutrophil phenotype in SCD patients differed from non-matched controls, in contrast to earlier studies, the differences in neutrophil phenotype between SCD patients and ethnicity-matched controls were modest.

Indexed as

Anemia, Sickle CellNeutrophilsAdolescentAdultCase-Control StudiesCell AdhesionFemaleHumansMaleMiddle AgedNeutrophil ActivationPhenotypeReactive Oxygen SpeciesYoung AdultReactive Oxygen Specieshemolysisneutrohil agingneutrophil activationneutrophil adhesionneutrophil phenotypereactive oxygen speciessickle cell disease

Identifiers

PMID40386776
PMCPMC12081264

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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.