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Role of alteration in Treg/Th17 cells’ balance in nephropathic patients with Type 2 diabetes mellitus

INTRODUCTION: In type 2 diabetes mellitus, the adaptive immune system drives systemic inflammation, promoting insulin resistance and related complications, such as diabetic nephropathy. Increased infiltration of activated T lymphocytes has been found in patients with diabetic nephropathy. T-cell inf...

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Autores principales: Abouzeid, Sameh, Sherif, Nevine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Electronic physician 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725415/
https://www.ncbi.nlm.nih.gov/pubmed/26816588
http://dx.doi.org/10.19082/1613
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author Abouzeid, Sameh
Sherif, Nevine
author_facet Abouzeid, Sameh
Sherif, Nevine
author_sort Abouzeid, Sameh
collection PubMed
description INTRODUCTION: In type 2 diabetes mellitus, the adaptive immune system drives systemic inflammation, promoting insulin resistance and related complications, such as diabetic nephropathy. Increased infiltration of activated T lymphocytes has been found in patients with diabetic nephropathy. T-cell influx and accumulation are the factors that aggravate diabetic nephropathy and link with glomerular filtration surface and albumin excretion. An appropriate balance between pro-inflammatory (T helper 17: Th17, and T helper 1: Th1) and anti-inflammatory (regulatory T cells: Tregs) subsets of T cells is critical to maintain homeostasis and avoid inflammatory disease. The aim of this study was to determine the balance between T helper 17 and regulatory T cells in type 2 diabetic patients who have diabetic nephropathy. METHODS: This case control study was conducted between December 2013 and June 2014 in Theodor Bilharz Research Institute in Egypt. Forty patients and 20 healthy volunteers were recruited in the study, and three groups were formed, i.e. two groups of cases with 20 patients in each group and one group of 20 controls) The groups were 1) 20 type 2 diabetic patients with nephropathy (group A); 2) 20 type 2 diabetic patients without nephropathy (group B); and 3) 20 healthy individuals (control group). Evaluation of T cells was done by standard 2-color flow cytometry. RESULTS: The study found higher mean of Th17 counts and Th17/Treg ratio among type 2 diabetic nephropathy patients compared to other groups; but a lower mean of Treg count was identified among type 2 diabetic nephropathy patients than in the other groups (p-value = 0.001). CONCLUSION: The important role for regulatory T cells in the protection against nephropathy in type 2 diabetic patients was demonstrated, and also it was observed that T helper 17 cells were associated with renal affection.
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spelling pubmed-47254152016-01-26 Role of alteration in Treg/Th17 cells’ balance in nephropathic patients with Type 2 diabetes mellitus Abouzeid, Sameh Sherif, Nevine Electron Physician Original Article INTRODUCTION: In type 2 diabetes mellitus, the adaptive immune system drives systemic inflammation, promoting insulin resistance and related complications, such as diabetic nephropathy. Increased infiltration of activated T lymphocytes has been found in patients with diabetic nephropathy. T-cell influx and accumulation are the factors that aggravate diabetic nephropathy and link with glomerular filtration surface and albumin excretion. An appropriate balance between pro-inflammatory (T helper 17: Th17, and T helper 1: Th1) and anti-inflammatory (regulatory T cells: Tregs) subsets of T cells is critical to maintain homeostasis and avoid inflammatory disease. The aim of this study was to determine the balance between T helper 17 and regulatory T cells in type 2 diabetic patients who have diabetic nephropathy. METHODS: This case control study was conducted between December 2013 and June 2014 in Theodor Bilharz Research Institute in Egypt. Forty patients and 20 healthy volunteers were recruited in the study, and three groups were formed, i.e. two groups of cases with 20 patients in each group and one group of 20 controls) The groups were 1) 20 type 2 diabetic patients with nephropathy (group A); 2) 20 type 2 diabetic patients without nephropathy (group B); and 3) 20 healthy individuals (control group). Evaluation of T cells was done by standard 2-color flow cytometry. RESULTS: The study found higher mean of Th17 counts and Th17/Treg ratio among type 2 diabetic nephropathy patients compared to other groups; but a lower mean of Treg count was identified among type 2 diabetic nephropathy patients than in the other groups (p-value = 0.001). CONCLUSION: The important role for regulatory T cells in the protection against nephropathy in type 2 diabetic patients was demonstrated, and also it was observed that T helper 17 cells were associated with renal affection. Electronic physician 2015-12-20 /pmc/articles/PMC4725415/ /pubmed/26816588 http://dx.doi.org/10.19082/1613 Text en © 2015 The Authors This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (http://creativecommons.org/licenses/by-nc-nd/3.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Original Article
Abouzeid, Sameh
Sherif, Nevine
Role of alteration in Treg/Th17 cells’ balance in nephropathic patients with Type 2 diabetes mellitus
title Role of alteration in Treg/Th17 cells’ balance in nephropathic patients with Type 2 diabetes mellitus
title_full Role of alteration in Treg/Th17 cells’ balance in nephropathic patients with Type 2 diabetes mellitus
title_fullStr Role of alteration in Treg/Th17 cells’ balance in nephropathic patients with Type 2 diabetes mellitus
title_full_unstemmed Role of alteration in Treg/Th17 cells’ balance in nephropathic patients with Type 2 diabetes mellitus
title_short Role of alteration in Treg/Th17 cells’ balance in nephropathic patients with Type 2 diabetes mellitus
title_sort role of alteration in treg/th17 cells’ balance in nephropathic patients with type 2 diabetes mellitus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725415/
https://www.ncbi.nlm.nih.gov/pubmed/26816588
http://dx.doi.org/10.19082/1613
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