Evidence map›Paper›PMID 42343201›Full record

ArticleBMC immunology2026

Cytokine and chemokine signatures of steady-state sickle cell disease in African children: a cross-sectional study.

Emmanuel Alote Allotey, David Adedia, Jones Amo Amponsah, Adjoa Agyemang Boakye, Augustina Frimpong, Jones Gyamfi, Elorm Ninsin, Hayford Offei, Henrietta Kwansa-Bentum, Grace Semabia Kpeli and 5 more

Abstract read
In one paragraph

Article in BMC immunology, 2026. 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Emmanuel Alote AlloteyWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Legon, Accra, Ghana.
David AdediaDepartment of Basic Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana.
Jones Amo AmponsahDepartment of Immunology, Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Accra, Ghana.
Adjoa Agyemang BoakyeDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana.
Augustina FrimpongDepartment of Immunology, Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Accra, Ghana.
Jones GyamfiDepartment of Medical Laboratory Sciences, School of Allied Health Sciences, University of Health and Allied Sciences, Ho, Ghana.
Elorm NinsinDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana.
Hayford OffeiDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana.
Henrietta Kwansa-BentumDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana.
Grace Semabia KpeliDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana.
John K A TettehDepartment of Immunology, Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Accra, Ghana.
Kokou Hefoume Amegan-AhoDepartment of Paediatrics, School of Medicine, University of Health and Allied Sciences, Ho, Ghana.
Peter Wisdom AtadjaDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana.
Lydia MosiWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Legon, Accra, Ghana.
Kwabena Obeng DueduDepartment of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Ghana. kwabena.duedu@bcu.ac.uk.ORCID https://orcid.org/0000-0001-5816-5172

Funding

DELTAS Africa DEL-15-007: Awandare
6 · The paper itself

Abstract

backgroundSickle cell disease (SCD) is characterized by chronic inflammation, yet the inflammatory landscape defining the clinically defined steady state remains poorly characterized, particularly in African populations where the disease burden is highest. Understanding baseline cytokine and chemokine signatures during the steady state is important for distinguishing physiological disease equilibrium from transitions toward acute complications.

methodsWe conducted a cross-sectional study of 129 children aged 2-17 years in Ghana, including 63 children with SCD in steady state and 66 healthy controls. Serum concentrations of 23 cytokines and chemokines were quantified using multiplex immunoassays alongside full blood count parameters. Comparative analyses and cytokine ratio assessments were performed to characterize steady-state SCD inflammatory signatures.

resultsMost pro-inflammatory cytokines and chemokines were significantly elevated in children with SCD compared with controls. However, IL-12p70 and IL-23p40 levels were significantly reduced in the SCD cohort, while CCL2 and IL-1β showed no significant differences between groups. Ratio analyses revealed lower IL-12p70/IL-4, IL-23p40/IL-4, and IL-1β/IL-10 ratios, alongside increased IL-1α/IL-4, IL-17A/IL-10, IL-3/IL-10, CCL3/IL-10, and GM-CSF/IL-10 ratios, indicating an imbalanced inflammatory milieu dominated by pro-inflammatory signals. Discriminant analyses using cytokine and hematological parameters further demonstrated clear separation between children with SCD and controls.

conclusionsSteady-state SCD in African children is characterized by a distinct cytokine and chemokine profile marked by persistent pro-inflammatory activation alongside regulatory counterbalances. Reduced ratios of IL-12p70 and IL-23p40 relative to anti-inflammatory cytokines may contribute to maintaining the steady-state inflammatory equilibrium. These findings provide reference signatures that may support future studies investigating inflammatory biomarkers.

Indexed as

Anemia, Sickle CellChemokinesCytokinesAdolescentBiomarkersChildChild, PreschoolCross-Sectional StudiesFemaleGhanaHumansInflammationMaleBiomarkersChemokinesCytokinesChildrenCytokinesHaemoglobinInflammationSickle Cell Disease

Identifiers

PMID42343201
PMCPMC13560138

What OpenQuestion holds

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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.