CD3+CD8+CD28− T Lymphocytes in Patients with Lupus Nephritis

The results of studies on the CD3+CD8+CD28- cells in SLE are inconsistent since several analyses describe CD3+CD8+CD28- as either immunosuppressive or cytotoxic. The aim of this study is to inquire whether the quantitative changes of CD3+CD8+CD28- T lymphocytes subpopulation are related to the clini...

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Main Authors: Marcelina Żabińska, Magdalena Krajewska, Katarzyna Kościelska-Kasprzak, Marian Klinger
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2016/1058165
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author Marcelina Żabińska
Magdalena Krajewska
Katarzyna Kościelska-Kasprzak
Marian Klinger
author_facet Marcelina Żabińska
Magdalena Krajewska
Katarzyna Kościelska-Kasprzak
Marian Klinger
author_sort Marcelina Żabińska
collection DOAJ
description The results of studies on the CD3+CD8+CD28- cells in SLE are inconsistent since several analyses describe CD3+CD8+CD28- as either immunosuppressive or cytotoxic. The aim of this study is to inquire whether the quantitative changes of CD3+CD8+CD28- T lymphocytes subpopulation are related to the clinical status of patients with lupus nephritis. Evaluation of Foxp3 expression on CD3+CD8+CD28- cells may shed some light on functional properties of these cells. 54 adult SLE patients and 19 sex and age matched healthy volunteers were enrolled in the study. There were 15 patients in inactive (SLEDAI ≤ 5) and 39 in active (SLEDAI > 5) phase of disease. We determined absolute count of CD3+CD8+CD28- and CD3+CD8+CD28-Foxp3+ subpopulations by flow cytometry. We observed a statistically significant increase in absolute count and percentage of CD3+CD8+CD28- in SLE patients compared to HC (p<0.001). Moreover there was significant positive correlation between increasing absolute count of CD3+CD8+CD28- cells and disease activity measured by SLEDAI (rs = 0.281, p=0.038). Active LN patients had increased absolute count of CD3+CD8+CD28- cells compared to HC. Positive correlation of CD3+CD8+CD28- number with disease activity, and lack of Foxp3 expression on these cells, suggests that CD3+CD8+CD28- lymphocytes might be responsible for an increased proinflammatory response in the exacerbation of SLE.
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spelling doaj-art-daaa865b728a41c7ab022d901a1d24262025-02-03T01:23:26ZengWileyJournal of Immunology Research2314-88612314-71562016-01-01201610.1155/2016/10581651058165CD3+CD8+CD28− T Lymphocytes in Patients with Lupus NephritisMarcelina Żabińska0Magdalena Krajewska1Katarzyna Kościelska-Kasprzak2Marian Klinger3Department and Clinic of Nephrology and Transplantation Medicine, Faculty of Postgraduate Medical Training, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandDepartment and Clinic of Nephrology and Transplantation Medicine, Faculty of Postgraduate Medical Training, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandDepartment and Clinic of Nephrology and Transplantation Medicine, Faculty of Postgraduate Medical Training, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandDepartment and Clinic of Nephrology and Transplantation Medicine, Faculty of Postgraduate Medical Training, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, PolandThe results of studies on the CD3+CD8+CD28- cells in SLE are inconsistent since several analyses describe CD3+CD8+CD28- as either immunosuppressive or cytotoxic. The aim of this study is to inquire whether the quantitative changes of CD3+CD8+CD28- T lymphocytes subpopulation are related to the clinical status of patients with lupus nephritis. Evaluation of Foxp3 expression on CD3+CD8+CD28- cells may shed some light on functional properties of these cells. 54 adult SLE patients and 19 sex and age matched healthy volunteers were enrolled in the study. There were 15 patients in inactive (SLEDAI ≤ 5) and 39 in active (SLEDAI > 5) phase of disease. We determined absolute count of CD3+CD8+CD28- and CD3+CD8+CD28-Foxp3+ subpopulations by flow cytometry. We observed a statistically significant increase in absolute count and percentage of CD3+CD8+CD28- in SLE patients compared to HC (p<0.001). Moreover there was significant positive correlation between increasing absolute count of CD3+CD8+CD28- cells and disease activity measured by SLEDAI (rs = 0.281, p=0.038). Active LN patients had increased absolute count of CD3+CD8+CD28- cells compared to HC. Positive correlation of CD3+CD8+CD28- number with disease activity, and lack of Foxp3 expression on these cells, suggests that CD3+CD8+CD28- lymphocytes might be responsible for an increased proinflammatory response in the exacerbation of SLE.http://dx.doi.org/10.1155/2016/1058165
spellingShingle Marcelina Żabińska
Magdalena Krajewska
Katarzyna Kościelska-Kasprzak
Marian Klinger
CD3+CD8+CD28− T Lymphocytes in Patients with Lupus Nephritis
Journal of Immunology Research
title CD3+CD8+CD28− T Lymphocytes in Patients with Lupus Nephritis
title_full CD3+CD8+CD28− T Lymphocytes in Patients with Lupus Nephritis
title_fullStr CD3+CD8+CD28− T Lymphocytes in Patients with Lupus Nephritis
title_full_unstemmed CD3+CD8+CD28− T Lymphocytes in Patients with Lupus Nephritis
title_short CD3+CD8+CD28− T Lymphocytes in Patients with Lupus Nephritis
title_sort cd3 cd8 cd28 t lymphocytes in patients with lupus nephritis
url http://dx.doi.org/10.1155/2016/1058165
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AT katarzynakoscielskakasprzak cd3cd8cd28tlymphocytesinpatientswithlupusnephritis
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