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NDT Advance Access originally published online on July 10, 2007
Nephrology Dialysis Transplantation 2007 22(12):3580-3585; doi:10.1093/ndt/gfm414
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© The Author [2007]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org



Bacterial DNA prolongs the survival of inflamed mononuclear cells in haemodialysis patients

Maria Dolores Navarro1, Julia Carracedo2, Rafael Ramírez2, Juan Antonio Madueño2, Ana Merino2, Mariano Rodríguez2, Alejandro Martín-Malo1 and Pedro Aljama1

1Servicio de Nefrología and 2Unidad de Investigación. Hospital Universitario. Reina Sofía, 14004 Córdoba, Spain

Correspondence and offprint requests to: Maria Dolores Navarro, Servicio de Nefrología, Hospital Universitario Reina Sofía, Avda Menendez Pidal s/n, Córdoba 14004. Spain. Email: mariad.navarro.sspa{at}juntadeandalucia.es



  Abstract

Background. Chronic kidney disease (CKD) patients show evidence of chronic inflammation with mononuclear cell activation which is mainly caused by uraemia itself and is exacerbated by haemodialysis. Small fragments of bacterial DNA (DNAb) are ubiquitous contaminants, which are capable of passing through dialyser membranes causing the stimulation of cells of the immune system. The aim of this study was to evaluate whether DNAb contamination may have an effect on apoptosis of activated monocytes from CKD-5 patients.

Methods. To test the ability of DNAb to stimulate the inflammatory response, mononuclear cells from 10 chronic kidney disease patients who had not begun haemodialysis (ND-CKD-5) and 10 patients undergoing regular dialysis (HD) were cultured in the presence and absence of DNAb. Ten healthy subjects were used as controls.

Results. The percentage of IL-1β cells was higher in HD patients than in ND-CKD-5 (33.9 ± 3.0% vs 20.0 ± 2.3%, P < 0.001) and controls (9.4 ± 2.1%, P < 0.001). The presence of DNAb induced an increase in the percent of cells expressing IL-1β in controls, ND-CKD5 and HD patients. In addition, the DNAb also increased the release of cytokines in all groups, the effect was more marked in ND-CKD5 and HD than in controls. DNAb only inhibited apoptosis of activated mononuclear cells from, ND-CKD (17.5 ± 2.8% vs 12.3 ± 2.6%, P < 0.01) and HD patients (27 ± 2.5% vs 14.6 ± 2.9%, P < 0.01).

Conclusions. DNAb enhances cytokine production and promotes the survival of inflammatory mononuclear cells from CKD patients. These results strongly suggest that DNAb fragments play an important role in maintaining chronic inflammation in patients on haemodialysis.

Keywords: apoptosis; bacterial DNA; chronic inflammation; cytokines; haemodialysis

Received for publication: 20. 3.07
Accepted in revised form: 1. 6.07


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