Effects of Different Levels of Endotoxin Contamination on Inflammatory Cytokine Production by Peripheral Blood Mononuclear Cells after High-Flux Hemodialysis
Article contributed by Mr CS Choong
Kearkiat Praditpornsilpaa, Khajohn Tiranathanagula, Paweena Susantitaphonga, Pisut Katavetina, Thananda Trakarnvanichb, Natavudh Townamchaia, Talerngsak Kanjanabucha, Yingyos Avihingsanona, Kriang Tungsangaa, Somchai Eiam-Onga
aDivision of Nephrology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, and
bRenal Unit, Department of Medicine, Bangkok Metropolitan Administration Medical College, Bangkok, Thailand
aDivision of Nephrology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, and
bRenal Unit, Department of Medicine, Bangkok Metropolitan Administration Medical College, Bangkok, Thailand
Blood Purif 2011;32:112-116 (DOI: 10.1159/000324394)
Abstract
Abstract
In Thailand, dialysate endotoxin contamination levels vary from less than 0.001 to 2.0 EU/ml. This difference has prompted an investigation on the production of proinflammatory cytokines and counter inflammatory mediators of peripheral blood mononuclear cells (PBMCs) after high-flux dialysis.
Methods:
Patients from four hemodialysis (HD) centers who met the inclusion/exclusion criteria were enrolled into the study. PBMCs were isolated by Ficoll density gradient centrifugation and cultured. Supernatants were tested for interleukin 6 (IL-6), IL-1β and IL-1 receptor antagonist (IL-1Ra) concentration by ELISA.
Results:
HD centers 1, 2, 3 and 4 had mean dialysate endotoxin contamination levels of 0.001, 0.026, 0.558 and 1.960 EU/ml, respectively. HD center 4 had the highest levels of IL-6 (1,052.3 ± 240.7 pg/106 PBMCs), IL-1β (1,297.1 ± 334.6 pg/106 PBMCs) and IL-1Ra (2,713.4 ± 1,255.3 pg/106 PBMCs). There were no significant differences in cytokine production between HD centers 1 and 2.
Conclusion:
Our study showed that ultrapure dialysate can minimize the risk of stimulating inflammatory cells. Ultrapure dialysate may prevent or delay endotoxin exposure-related complications.
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