open access

Vol 2, No 1 (2017)
Original article
Published online: 2017-09-21
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Flow cytometric evaluation of T and B lymphocyte percentage in chronic kidney disease

Tülay Kılıçaslan Ayna12, Burcu Akman, Aslı Özkızılcık Koçyiğit, Derya Güleç, Cem Tugmen, Mustafa Soyöz12
·
Medical Research Journal 2017;2(1):29-33.
Affiliations
  1. Department of Medical Biology and Genetics, Izmir Katip Celebi University, Izmir, Turkey, Türkiye
  2. Tissue Typing Laboratory, University of Health Science Tepecik Training and Research Hospital, Izmir, Türkiye

open access

Vol 2, No 1 (2017)
ORIGINAL ARTICLES
Published online: 2017-09-21

Abstract

Introduction. T and B lymphocytes play crucial roles in adaptive immunity. These cells are negatively affected in multiple disorders, including chronic kidney disease. The purpose of this study was to compare T and B lymphocyte ratios between patients with chronic kidney disease and healthy controls.

Methods. In this study, we evaluated the percentages of patient and donor (healthy control) lymphocytes referred to our laboratory between 2012 and 2014. In total 103 patient-donor couples were tested by the FCXM method. CD3-PerCP and CD19-PE monoclonal antibodies were used in order to differentiate T and B cells, respectively. T and B cell percentages of the participants were statistically compared.

Results. The mean age of the investigated patients and donors was 36.3 ± 13.7 and 46.2 ± 12.4 years, respectively. Of the studied patients, 45.6% and 54.3% were female and male, whereas 54.3% and 45.6% of donors were female and male, respectively. In the investigated group, 42 patients were preemptive, 45 subjects were treated with haemodialysis, and 16 individuals were on peritoneal dialysis. T and B lymphocyte percentages in the healthy group were higher than in patients with chronic kidney disease. However, the difference reached statistical significance only for T lymphocytes (p < 0.05). The percentages of total lymphocytes, and T and B lymphocytes in patients treated with haemodialysis were numerically lower than in those on peritoneal dialysis. In addition, we found that patients with chronic kidney disease had lower concentrations of haemoglobin and albumin than healthy controls.

Conclusion. This study suggests that patients with advanced chronic kidney disease have lower rates of lymphocytes that healthy controls. This fact may at least partially explain impaired immunity in this setting. However, our findings require confirmation and detailed investigation of underlying mechanisms in further studies.  

Abstract

Introduction. T and B lymphocytes play crucial roles in adaptive immunity. These cells are negatively affected in multiple disorders, including chronic kidney disease. The purpose of this study was to compare T and B lymphocyte ratios between patients with chronic kidney disease and healthy controls.

Methods. In this study, we evaluated the percentages of patient and donor (healthy control) lymphocytes referred to our laboratory between 2012 and 2014. In total 103 patient-donor couples were tested by the FCXM method. CD3-PerCP and CD19-PE monoclonal antibodies were used in order to differentiate T and B cells, respectively. T and B cell percentages of the participants were statistically compared.

Results. The mean age of the investigated patients and donors was 36.3 ± 13.7 and 46.2 ± 12.4 years, respectively. Of the studied patients, 45.6% and 54.3% were female and male, whereas 54.3% and 45.6% of donors were female and male, respectively. In the investigated group, 42 patients were preemptive, 45 subjects were treated with haemodialysis, and 16 individuals were on peritoneal dialysis. T and B lymphocyte percentages in the healthy group were higher than in patients with chronic kidney disease. However, the difference reached statistical significance only for T lymphocytes (p < 0.05). The percentages of total lymphocytes, and T and B lymphocytes in patients treated with haemodialysis were numerically lower than in those on peritoneal dialysis. In addition, we found that patients with chronic kidney disease had lower concentrations of haemoglobin and albumin than healthy controls.

Conclusion. This study suggests that patients with advanced chronic kidney disease have lower rates of lymphocytes that healthy controls. This fact may at least partially explain impaired immunity in this setting. However, our findings require confirmation and detailed investigation of underlying mechanisms in further studies.  

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Keywords

chronic kidney disease, dialysis, lymphocyte, flow cytometry, haemoglobin

About this article
Title

Flow cytometric evaluation of T and B lymphocyte percentage in chronic kidney disease

Journal

Medical Research Journal

Issue

Vol 2, No 1 (2017)

Article type

Original article

Pages

29-33

Published online

2017-09-21

Page views

738

Article views/downloads

915

DOI

10.5603/MRJ.2017.0005

Bibliographic record

Medical Research Journal 2017;2(1):29-33.

Keywords

chronic kidney disease
dialysis
lymphocyte
flow cytometry
haemoglobin

Authors

Tülay Kılıçaslan Ayna
Burcu Akman
Aslı Özkızılcık Koçyiğit
Derya Güleç
Cem Tugmen
Mustafa Soyöz

References (12)
  1. Plantinga LC, Boulware LE, Coresh J, et al. Patient awareness of chronic kidney disease: trends and predictors. Arch Intern Med. 2008; 168(20): 2268–2275.
  2. Süleymanlar G, Altıparmak MR, Seyahi N, Trabulus S. Registry of Nephrology, Dialysis, and Transplantation in Turkey. The Turkish Society of Nephrology 2013.
  3. Pahl MV, Gollapudi S, Sepassi L, et al. Effect of end-stage renal disease on B-lymphocyte subpopulations, IL-7, BAFF and BAFF receptor expression. Nephrol Dial Transplant. 2010; 25(1): 205–212.
  4. Zaher MM, Gaber A, Alrefaey AA, et al. Assessment of some trace elements: copper, zinc and magnesium and their impact on CD3 and CD4 levels in children on chronic hemodialysis. Life Sci J. 2013; 10: 222–230.
  5. Lisowska KA, Dębska-Ślizień A, Jasiulewicz A, et al. Influence of hemodialysis on circulating CD4(low)CD25 (high) regulatory T cells in end-stage renal disease patients. Inflamm Res. 2014; 63(2): 99–103.
  6. Pahl MV, Gollapudi S, Sepassi L, et al. Effect of end-stage renal disease on B-lymphocyte subpopulations, IL-7, BAFF and BAFF receptor expression. Nephrol Dial Transplant. 2010; 25(1): 205–212.
  7. Grooteman MP, Nube MJ, van Limbeek J, et al. Lymphocyte subsets in dialyser eluates: a new parameter of bioincompatibility? Nephrol Dial Transplant. 1996; 11(6): 1073–1078.
  8. Lisowska KA, Dębska-Ślizień A, Jasiulewicz A, et al. Hemodialysis affects phenotype and proliferation of CD4-positive T lymphocytes. J Clin Immunol. 2012; 32(1): 189–200.
  9. Westermann J, Pabst R. Lymphocyte subsets in the blood: a diagnostic window on the lymphoid system? Immunol Today. 1990; 11(11): 406–410.
  10. Lang CL, Wang MH, Hung KY, et al. Correlation of interleukin-17-producing effector memory T cells and CD4+CD25+Foxp3 regulatory T cells with the phosphate levels in chronic hemodialysis patients. Scientific World Journal. 2014; 2014: 593170.
  11. Grzegorzewska AE, Leander M, Grzegorzewska AE, et al. Lymphocyte subsets in the course of continuous ambulatory peritoneal dialysis. Adv Perit Dial. 2001; 17: 10–14.
  12. Alvarez-Lara MA, Carracedo J, Ramírez R, et al. The imbalance in the ratio of Th1 and Th2 helper lymphocytes in uraemia is mediated by an increased apoptosis of Th1 subset. Nephrol Dial Transplant. 2004; 19(12): 3084–3090.

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