Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (19)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Sester, U.
Right arrow Articles by Köhler, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sester, U.
Right arrow Articles by Köhler, H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nephrol Dial Transplant (2001) 16: 1402-1408
© 2001 European Renal Association-European Dialysis and Transplant Association

Strong depletion of CD14+CD16+ monocytes during haemodialysis treatment

Urban Sester, Martina Sester, Gunnar Heine, Harald Kaul, Matthias Girndt and Hans Köhler

Medical Department IV, Nephrology, University of the Saarland, Homburg, Germany

Background. The immune defect in haemodialysis (HD) patients is associated with a monocytic dysfunction, including an increased production of proinflammatory cytokines. Monocytes fall into subpopulations comprising CD14++CD16- and CD14+CD16+ cells. Circulating numbers of the latter can rapidly increase during infectious episodes and inflammation.

Methods. We determined the amount of CD14+CD16+ monocytes in HD patients and characterized their fate during HD treatment. In 34 HD patients and 17 healthy controls, the distinct cell populations were determined by differential blood counts and flow cytometry. Cells from 14 HD patients were analysed at the start, 10, 30 and 120 min thereafter, and at the end of HD treatment.

Results. Before HD, patients show a monocytosis with a strongly increased CD14+CD16+ subpopulation. Early during HD treatment, circulating leukocyte numbers decrease, with monocytes being most profoundly influenced. Interestingly, among them, sequestration is most pronounced in the CD14+ CD16+ subpopulation. After 30 min, ~83±9% of CD14+CD16+ cells are removed from circulation. This sequestration does not differ between patients treated with polyamide or haemophan membranes. The sequestration is a short-lived temporary effect and cell numbers are replenished within 120 min of treatment for the entire monocyte population. Beyond that time point, cellular activation by the dialyser membrane becomes visible. Reappearence kinetics of CD14+CD16+ monocytes is slower; however, initial numbers are reached by the end of treatment.

Conclusion. Haemodiaysis leads to temporary removal of monocytes from the bloodstream followed by the reappearance of activated cells. This might contribute to the state of chronic microinflammation, which is reflected by high levels of CD14+CD16+ monocytes.

Keywords: CD14+CD16+ monocytes; flow cytometry; haemodialysis; inflammation

Correspondence and offprint requests to: Prof. Dr Hans Köhler, Medical Department IV, Nephrology, University Homburg, D-66421 Homburg, Germany.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nephrol Dial TransplantHome page
K. S. Rogacev, M. Ziegelin, C. Ulrich, S. Seiler, M. Girndt, D. Fliser, and G. H. Heine
Haemodialysis-induced transient CD16+ monocytopenia and cardiovascular outcome
Nephrol. Dial. Transplant., November 1, 2009; 24(11): 3480 - 3486.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
P. E. Westerweel, I. E. Hoefer, P. J. Blankestijn, P. de Bree, D. Groeneveld, O. van Oostrom, B. Braam, H. A. Koomans, and M. C. Verhaar
End-stage renal disease causes an imbalance between endothelial and smooth muscle progenitor cells
Am J Physiol Renal Physiol, April 1, 2007; 292(4): F1132 - F1140.
[Abstract] [Full Text] [PDF]


Home page
J. Leukoc. Biol.Home page
L. Ziegler-Heitbrock
The CD14+ CD16+ blood monocytes: their role in infection and inflammation
J. Leukoc. Biol., March 1, 2007; 81(3): 584 - 592.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
J. Carracedo, A. Merino, S. Nogueras, D. Carretero, I. Berdud, R. Ramirez, C. Tetta, M. Rodriguez, A. Martin-Malo, and P. Aljama
On-Line Hemodiafiltration Reduces the Proinflammatory CD14+CD16+ Monocyte-Derived Dendritic Cells: A Prospective, Crossover Study
J. Am. Soc. Nephrol., August 1, 2006; 17(8): 2315 - 2321.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
C. Ulrich, G. H. Heine, P. Garcia, B. Reichart, T. Georg, M. Krause, H. Kohler, and M. Girndt
Increased expression of monocytic angiotensin-converting enzyme in dialysis patients with cardiovascular disease
Nephrol. Dial. Transplant., June 1, 2006; 21(6): 1596 - 1602.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
G. Pertosa, S. Simone, M. Soccio, D. Marrone, L. Gesualdo, F. P. Schena, and G. Grandaliano
Coagulation Cascade Activation Causes CC Chemokine Receptor-2 Gene Expression and Mononuclear Cell Activation in Hemodialysis Patients
J. Am. Soc. Nephrol., August 1, 2005; 16(8): 2477 - 2486.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
A. H. M. Bouts, R. T. Krediet, J.-C. Davin, L. A. H. Monnens, J. Nauta, C. H. Schroder, J. G. J. van de Winkel, and T. A. Out
IGG and complement receptor expression on peripheral white blood cells in uraemic children
Nephrol. Dial. Transplant., September 1, 2004; 19(9): 2296 - 2301.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.