C5a receptor modulation on neutrophils and monocytes from chronic hemodialysis and peritoneal dialysis patients

S. L. Lewis, D. E. Van Epps, D. E. Chenoweth

    Research output: Contribution to journalArticle

    23 Scopus citations

    Abstract

    Chronic renal failure patients have an increased risk for infection which may partially be due to altered chemotactic ability of their white blood cells. This study was designed to evaluate chemotactic factor and Fc receptor expression on neutrophils (PMN) and monocytes from chronic renal failure patients on hemodialysis (HD) or continuous ambulatory peritoneal dialysis (CAPD). Analysis of these receptors was performed using flow cytometry and fluorescent chemotactic factors (C5a, f-Met-Leu-Phe-Lys [fMLPL] and casein) and heat-aggregated human IgG. Peripheral blood PMN and monocytes obtained from 14 HD patients (in the predialysis period) and 14 CAPD patients were analyzed for their ability to bind each of the fluoresceinated ligands. PMN and monocytes from both patient groups had a significant reduction in their ability to bind C5a. The average percentage (± s.e.m.) of PMN that bound C5a was 93.9 ± 1.1 for the controls, 72.9 ± 3.8 for HD patients, and 79.3 ± 4.0 for CAPD patients. Similar results were obtained with monocytes with 69.7 ± 1.9% for controls, 54.6 ± 4.5% for HD patients, and 31.0 ± 4.5% for CAPD patients. These differences in C5a binding were also reflected in the average intensity of fluorescence. There was no significant difference in the percentage or fluorescence intensity of PMN or monocytes that bound casein or aggregated IgG when either group of dialysis patients was compared to the control values. Binding of fMLPL by PMN and monocytes from the HD patients and PMN from the CAPD patients were similar to control values but the binding of fMLPL by monocytes from CAPD patients was significantly suppressed (p < 0.03). Both HD and CAPD patients had elevated levels of plasma C3a indicating chronic complement activation. These results demonstrate decreased C5a receptor availability on PMN and monocyte in both patient populations which may contribute to these patients' increased risk to infection by reducing the ability of these cells to respond to C5a generated at a site of infection.

    Original languageEnglish (US)
    Pages (from-to)37-44
    Number of pages8
    JournalClinical Nephrology
    Volume26
    Issue number1
    StatePublished - Jan 1 1986

      Fingerprint

    ASJC Scopus subject areas

    • Nephrology

    Cite this