The role of regulatory CD4+CD25+high T-lymphocytes and their functional activity in the development of type 1 diabetes mellitus

Type 1 diabetes mellitus (DM1) is associated with compromised (defective) immunologic tolerance to autoantigens and selective destruction of pancreatic B-cells by CD4+ (effector) and CD8 (cytotoxic) lymphocytes. The mechanisms of autotolerance involve CD4+CD25+high T-regulatory cells (Treg) whose su...

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Autores principales: Tatiana Vasil'evna Nikonova, Pavel Vasil'evich Apanovich, Elena Vladimirovna Pekareva, Vera Anatol'evna Gorelysheva, Sergey Alexandrovich Prokof'ev, Alexander Vasil'evich Karpukhin, Ivan Ivanovich Dedov
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Publicado: Endocrinology Research Centre 2010
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spelling oai:doaj.org-article:d25393636268490b95fce9d3182b0abb2021-11-14T09:00:15ZThe role of regulatory CD4+CD25+high T-lymphocytes and their functional activity in the development of type 1 diabetes mellitus2072-03512072-037810.14341/2072-0351-5483https://doaj.org/article/d25393636268490b95fce9d3182b0abb2010-09-01T00:00:00Zhttps://www.dia-endojournals.ru/jour/article/view/5483https://doaj.org/toc/2072-0351https://doaj.org/toc/2072-0378Type 1 diabetes mellitus (DM1) is associated with compromised (defective) immunologic tolerance to autoantigens and selective destruction of pancreatic B-cells by CD4+ (effector) and CD8 (cytotoxic) lymphocytes. The mechanisms of autotolerance involve CD4+CD25+high T-regulatory cells (Treg) whose suppressor activity depends on the expression of the FoxP3 gene. Aim. Detection of quantitative and functional alterations at the level of regulation of immunity in subjects at risk of DM1 and patients with different duration of DM1. Materials and methods. 116 patients (67 men and 49 women) with different duration of DM1. The risk group was comprised of 33 subjects (10 men and 23 women), control group included 16 subjects. In all cases, HLA genotyping was performed, autoantibodies to GDC, insulin and tyrosine phosphatase, islet cell antigens were determined, subpopulation composition of CD3+, CD4+, CD8+, CD38+, HLA DR+, CD25+, CD4+25+ lymphocytes and their functional activities (FoxP3 gene expression) studied, C-peptie and HbA1c levels measured. Results. A tendency toward a rise in Cd25+ and CD4+25+ T-lymphocytes and a decrease in FoxP3 expression was documented in the risk group compared with control (p0.05) but their functional activity was lower (pTatiana Vasil'evna NikonovaPavel Vasil'evich ApanovichElena Vladimirovna PekarevaVera Anatol'evna GorelyshevaSergey Alexandrovich Prokof'evAlexander Vasil'evich KarpukhinIvan Ivanovich DedovEndocrinology Research Centrearticletype 1 diabetes mellitussubjects at risk if dm1cd4+cd25+high regulatory t-lymphocytesfoxp3 geneNutritional diseases. Deficiency diseasesRC620-627ENRUСахарный диабет, Vol 13, Iss 3, Pp 25-31 (2010)
institution DOAJ
collection DOAJ
language EN
RU
topic type 1 diabetes mellitus
subjects at risk if dm1
cd4+cd25+high regulatory t-lymphocytes
foxp3 gene
Nutritional diseases. Deficiency diseases
RC620-627
spellingShingle type 1 diabetes mellitus
subjects at risk if dm1
cd4+cd25+high regulatory t-lymphocytes
foxp3 gene
Nutritional diseases. Deficiency diseases
RC620-627
Tatiana Vasil'evna Nikonova
Pavel Vasil'evich Apanovich
Elena Vladimirovna Pekareva
Vera Anatol'evna Gorelysheva
Sergey Alexandrovich Prokof'ev
Alexander Vasil'evich Karpukhin
Ivan Ivanovich Dedov
The role of regulatory CD4+CD25+high T-lymphocytes and their functional activity in the development of type 1 diabetes mellitus
description Type 1 diabetes mellitus (DM1) is associated with compromised (defective) immunologic tolerance to autoantigens and selective destruction of pancreatic B-cells by CD4+ (effector) and CD8 (cytotoxic) lymphocytes. The mechanisms of autotolerance involve CD4+CD25+high T-regulatory cells (Treg) whose suppressor activity depends on the expression of the FoxP3 gene. Aim. Detection of quantitative and functional alterations at the level of regulation of immunity in subjects at risk of DM1 and patients with different duration of DM1. Materials and methods. 116 patients (67 men and 49 women) with different duration of DM1. The risk group was comprised of 33 subjects (10 men and 23 women), control group included 16 subjects. In all cases, HLA genotyping was performed, autoantibodies to GDC, insulin and tyrosine phosphatase, islet cell antigens were determined, subpopulation composition of CD3+, CD4+, CD8+, CD38+, HLA DR+, CD25+, CD4+25+ lymphocytes and their functional activities (FoxP3 gene expression) studied, C-peptie and HbA1c levels measured. Results. A tendency toward a rise in Cd25+ and CD4+25+ T-lymphocytes and a decrease in FoxP3 expression was documented in the risk group compared with control (p0.05) but their functional activity was lower (p
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author Tatiana Vasil'evna Nikonova
Pavel Vasil'evich Apanovich
Elena Vladimirovna Pekareva
Vera Anatol'evna Gorelysheva
Sergey Alexandrovich Prokof'ev
Alexander Vasil'evich Karpukhin
Ivan Ivanovich Dedov
author_facet Tatiana Vasil'evna Nikonova
Pavel Vasil'evich Apanovich
Elena Vladimirovna Pekareva
Vera Anatol'evna Gorelysheva
Sergey Alexandrovich Prokof'ev
Alexander Vasil'evich Karpukhin
Ivan Ivanovich Dedov
author_sort Tatiana Vasil'evna Nikonova
title The role of regulatory CD4+CD25+high T-lymphocytes and their functional activity in the development of type 1 diabetes mellitus
title_short The role of regulatory CD4+CD25+high T-lymphocytes and their functional activity in the development of type 1 diabetes mellitus
title_full The role of regulatory CD4+CD25+high T-lymphocytes and their functional activity in the development of type 1 diabetes mellitus
title_fullStr The role of regulatory CD4+CD25+high T-lymphocytes and their functional activity in the development of type 1 diabetes mellitus
title_full_unstemmed The role of regulatory CD4+CD25+high T-lymphocytes and their functional activity in the development of type 1 diabetes mellitus
title_sort role of regulatory cd4+cd25+high t-lymphocytes and their functional activity in the development of type 1 diabetes mellitus
publisher Endocrinology Research Centre
publishDate 2010
url https://doaj.org/article/d25393636268490b95fce9d3182b0abb
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