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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
  • , John K. A. Tetteh
  • , Kokou Hefoume Amegan-Aho
  • , Peter Wisdom Atadja
  • , Lydia Mosi
  • , Kwabena Obeng Duedu (Corresponding / Lead Author)

Research output: Contribution to journalArticlepeer-review

Abstract

Sickle 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.
Original languageEnglish
JournalBMC Immunology
DOIs
Publication statusPublished (VoR) - 24 Jun 2026

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