Influence of hemodialysis on circulating CD4 low CD25 high regulatory T cells in end-stage renal disease patients

18Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Objective: Immunodeficiency of end-stage renal disease (ESRD) is caused by several factors including uremic toxins and biocompatibility reactions due to the repeated hemodialysis (HD) procedure. It has also been suggested that poor T cell responses could be associated with the increased number of regulatory T cells (Tregs) which are necessary to limit the function of activated T cells. The aim of the study was to determine the proportion of CD4 + CD25 + cells (activated T cells) to CD4 low CD25 high cells (Tregs) within the CD4 + population in ESRD patients. Patients and methods: Two groups of ESRD patients, predialysis patients treated conservatively and patients undergoing hemodialysis (HD), as well as healthy controls were included in the study. Percentages of activated and regulatory T cells were determined ex vivo with flow cytometry based on the expression of CD4 and CD25 antigens. Results and conclusions: HD patients showed an increased percentage of CD4 + CD25 + cells when compared with healthy controls, while there was no difference in the percentage of CD4 low CD25 high cells between the patient groups. In our opinion, the repeated hemodialysis procedure significantly disturbs the balance between activated T cells and regulatory T cells in ESRD patients. Lack of Treg mobilization and chronic stimulation of T cells may contribute to the immune deficiency observed in these patients. © 2013 Springer Basel.

Cite

CITATION STYLE

APA

Lisowska, K. A., Dębska-Ślizień, A., Jasiulewicz, A., Bryl, E., & Witkowski, J. M. (2014). Influence of hemodialysis on circulating CD4 low CD25 high regulatory T cells in end-stage renal disease patients. Inflammation Research, 63(2), 99–103. https://doi.org/10.1007/s00011-013-0679-z

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free