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Peritoneal macrophage beta-2 microglobulin production and bacterial peritonitis in CAPD patients

S Carozzi1, G Nasini, C Schelotto

  • 1Nephrology and Dialysis Unit, St. Paul's Hospital, Savona, Italy.

ASAIO Transactions
|July 1, 1990
PubMed

Insights

Bacterial peritonitis in continuous ambulatory peritoneal dialysis (CAPD) patients significantly increases peritoneal macrophage (PM) production of Beta-2 Microglobulin (B2M), Interleukin-1 (IL-1), and Leukotriene B4 (LTB4). This suggests a cytokine-mediated process during infection.

Area of Science:

  • Nephrology
  • Immunology
  • Peritoneal Dialysis

Background:

  • Bacterial peritonitis is a complication in continuous ambulatory peritoneal dialysis (CAPD).
  • Peritoneal macrophages (PM) play a role in the inflammatory response.
  • Beta-2 Microglobulin (B2M), Interleukin-1 (IL-1), and Leukotriene B4 (LTB4) are inflammatory markers.

Purpose of the Study:

  • To investigate the impact of bacterial peritonitis on PM production of B2M, IL-1, and LTB4 in CAPD patients.
  • To explore the relationship between these markers and PM release.
  • To compare findings with hemodialysis (HD) patients.

Main Methods:

  • Studied 20 CAPD patients (10 with peritonitis) and 30 HD patients.
  • Measured in vivo plasma and peritoneal dialysis effluent (PDE) levels of B2M, IL-1, and LTB4.
  • Assessed in vitro B2M, IL-1, and LTB4 release by PM and peripheral blood monocytes.

Main Results:

  • CAPD patients with peritonitis showed significantly higher PDE concentrations of B2M, IL-1, and LTB4 compared to those without peritonitis.
  • In vitro PM from peritonitis patients produced higher levels of these markers.
  • Elevated levels in CAPD peritonitis patients were comparable to HD patients treated with Cuprophan (CU) membranes.

Conclusions:

  • Bacterial peritonitis induces PM B2M production in CAPD patients.
  • This induction is likely mediated by cytokines.
  • The process may be similar to that observed in HD patients treated with CU membranes.

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