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Published on: December 19, 2010
Intraperitoneal interleukin-8 and neutrophil influx in the initial phase of a CAPD peritonitis
M G Betjes1, C E Visser, D Zemel
1Department of Cell Biology, Vrije Universiteit, Amsterdam, The Netherlands.
Insights
Interleukin-8 (IL-8) levels in peritoneal dialysis fluid rise before peritonitis develops, indicating its role in attracting neutrophils during continuous ambulatory peritoneal dialysis (CAPD) peritonitis.
Area of Science:
- Nephrology
- Immunology
- Peritoneal Dialysis
Background:
- Peritonitis is a serious complication of continuous ambulatory peritoneal dialysis (CAPD).
- Early detection and understanding of peritonitis mechanisms are crucial for patient management.
Purpose of the Study:
- To determine if dialysate interleukin-8 (IL-8) concentration changes precede clinical peritonitis onset in CAPD patients.
- To assess IL-8's role in granulocyte recruitment during CAPD-related peritonitis.
Main Methods:
- Overnight peritoneal dialysis effluent samples were collected and stored from CAPD patients.
- Samples from before and during peritonitis episodes, along with post-recovery controls, were analyzed for cell counts, IL-8, and elastase.
- Neutrophil chemoattractant capacity of effluents was assessed in vitro.
Main Results:
- Dialysate IL-8 and elastase levels, along with neutrophil numbers, increased 4–12 hours prior to overt peritonitis.
- A significant correlation was observed between dialysate IL-8 and neutrophil count.
- IL-8 in peritoneal fluid contributes to neutrophil recruitment in early CAPD peritonitis.
Conclusions:
- Dialysate IL-8 elevation is an early indicator of impending CAPD peritonitis.
- IL-8 plays a significant role in neutrophil recruitment and activation during the initial stages of CAPD peritonitis.
Objective:
To investigate whether or not a change in dialysate interleukin-8 (IL-8) concentration precedes the onset of clinically overt peritonitis and is significant in the recruitment of granulocytes during continuous ambulatory peritoneal dialysis (CAPD)-related peritonitis.
Design:
CAPD patients stored their overnight effluent at 4 degrees C, which was routinely thrown away after 2 days. If peritonitis developed, patients delivered their effluent of the preceding two nights and the peritonitis effluent for analysis. A control study was performed 1 to 3 months after recovery. Dialysate samples were analyzed for number of cells, differential cell count, IL-8 and elastase concentrations, and their neutrophil chemoattractive capacity. In addition, serum samples during peritonitis were analyzed for IL-8 concentrations.
Results:
Ten peritonitis episodes in 7 patients were analyzed. Numbers of neutrophils and levels of dialysate IL-8 and elastase started to increase 4 to 12 hours before the first peritonitis effluent. The dialysate/serum IL-8 ratio was 423.5 during peritonitis and 7.0 in the postperitonitis controls. There was a significant correlation between the number of neutrophils and IL-8 concentration in the dialysate. The in vitro neutrophil chemotaxis was increased toward the peritonitis effluents, as compared to control effluents. Incubation of the peritonitis effluents with anti-IL-8 monoclonal antibody blocked the increase in neutrophil chemotaxis above control levels by an average of 26.7%.
Conclusion:
IL-8 is produced in the peritoneal cavity during CAPD treatment and may mediate part of the neutrophil recruitment and degranulation in the initial phase of a CAPD peritonitis.
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