Investigation of exosomal tetraspanin profile in sepsis patients as a promising diagnostic biomarker

Biomarkers. 2024 Mar;29(2):78-89. doi: 10.1080/1354750X.2024.2319296. Epub 2024 Feb 20.

Abstract

Introduction: Sepsis, a leading cause of mortality globally, has a complex and multifaceted pathophysiology which still requires elucidation. Therefore, this study aimed to analyze and quantify the number of exosomes in sepsis patients from a South African cohort using the ExoView (NanoView Biosciences, Boston, MA) platform.

Methods: Blood samples were collected from black South African patients attending the local Intensive Care Unit (ICU) hospital. Exosomes were isolated and characterize via TEM and CD63 ELISA kits. ExoView was used to determine particle count, particle size distribution and colocalization of different tetraspanin markers.

Results: Exosomal levels in sepsis patients were significantly higher compared to the control group (p < 0.05). Sepsis exosomes showed a homogenous size distribution ranging from 55 to 70 nm. Tetraspanin colocalization analysis revealed that sepsis exosomes have significantly higher CD63/CD9, CD63/CD81 and CD63/CD9/CD81 colocalization percentages than the control group.

Conclusion: This unique tetraspanin colocalization pattern of sepsis exosomes could serve as a potential sepsis biomarker. Further investigations are required to identify sepsis exosomal cargo signatures for further understanding of sepsis pathophysiology in order to develop effective diagnostics and treatments.

Keywords: ExoView; Sepsis; colocalization; exosomes; pathophysiology; tetraspanin.

MeSH terms

  • Biomarkers / analysis
  • Exosomes*
  • Humans
  • Sepsis* / diagnosis
  • Tetraspanin 30 / analysis
  • Tetraspanins / analysis

Substances

  • Tetraspanin 30
  • Tetraspanins
  • Biomarkers