Cargando…
Numerical status of CD4(+)CD25(+)FoxP3(+) and CD8(+)CD28(-) regulatory T cells in multiple sclerosis
OBJECTIVE(S): Regulatory T cells, including CD4+CD25+Fox3+ and CD8+CD28- cells play an important role in regulating the balance between immunity and tolerance. Since multiple sclerosis is an inflammatory autoimmune disease, regulatory T cells are considered to be involved in its pathogenesis. In thi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046232/ https://www.ncbi.nlm.nih.gov/pubmed/24904717 |
_version_ | 1782480256705232896 |
---|---|
author | Kouchaki, Ebrahim Salehi, Mahdi Reza Sharif, Mohammad Nikoueinejad, Hassan Akbari, Hossein |
author_facet | Kouchaki, Ebrahim Salehi, Mahdi Reza Sharif, Mohammad Nikoueinejad, Hassan Akbari, Hossein |
author_sort | Kouchaki, Ebrahim |
collection | PubMed |
description | OBJECTIVE(S): Regulatory T cells, including CD4+CD25+Fox3+ and CD8+CD28- cells play an important role in regulating the balance between immunity and tolerance. Since multiple sclerosis is an inflammatory autoimmune disease, regulatory T cells are considered to be involved in its pathogenesis. In this study, we investigated the circulatory numbers of the two mentioned types of regulatory T cells and also their association with different clinical characteristics in 84 multiple sclerosis patients. MATERIALS AND METHODS: 84 patients with multiple sclerosis and 75 normal individuals were studied. Demographic and clinical information of all participants were collected via questionnaire and clinical examination as well as MRI. The peripheral blood frequency of two different subgroups of regulatory T cells (CD4+ CD25+Foxp3+ and CD8+CD28- cells) were analyzed by flow cytometry using anti-human antibodies conjugated with CD4-FITC / CD25-PE/Foxp3-PE-Cy5, CD3-PE/CD8a-PE-Cy5/CD28-FITC. RESULTS: The frequency of CD4+CD25+Foxp3+ cells in multiple sclerosis patients was significantly less than that in healthy controls (P=0.006) and in mild forms less than that in sever forms (P=0.003). There was not any correlation between the frequency of regulatory T cells and different clinical variables. CONCLUSION: Our results showed that the number of CD4+CD25+Foxp3+ cells decreases significantly in multiple sclerosis patients, which probably shows the regulatory role of these cells in multiple sclerosis. |
format | Online Article Text |
id | pubmed-4046232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-40462322014-06-05 Numerical status of CD4(+)CD25(+)FoxP3(+) and CD8(+)CD28(-) regulatory T cells in multiple sclerosis Kouchaki, Ebrahim Salehi, Mahdi Reza Sharif, Mohammad Nikoueinejad, Hassan Akbari, Hossein Iran J Basic Med Sci Original Article OBJECTIVE(S): Regulatory T cells, including CD4+CD25+Fox3+ and CD8+CD28- cells play an important role in regulating the balance between immunity and tolerance. Since multiple sclerosis is an inflammatory autoimmune disease, regulatory T cells are considered to be involved in its pathogenesis. In this study, we investigated the circulatory numbers of the two mentioned types of regulatory T cells and also their association with different clinical characteristics in 84 multiple sclerosis patients. MATERIALS AND METHODS: 84 patients with multiple sclerosis and 75 normal individuals were studied. Demographic and clinical information of all participants were collected via questionnaire and clinical examination as well as MRI. The peripheral blood frequency of two different subgroups of regulatory T cells (CD4+ CD25+Foxp3+ and CD8+CD28- cells) were analyzed by flow cytometry using anti-human antibodies conjugated with CD4-FITC / CD25-PE/Foxp3-PE-Cy5, CD3-PE/CD8a-PE-Cy5/CD28-FITC. RESULTS: The frequency of CD4+CD25+Foxp3+ cells in multiple sclerosis patients was significantly less than that in healthy controls (P=0.006) and in mild forms less than that in sever forms (P=0.003). There was not any correlation between the frequency of regulatory T cells and different clinical variables. CONCLUSION: Our results showed that the number of CD4+CD25+Foxp3+ cells decreases significantly in multiple sclerosis patients, which probably shows the regulatory role of these cells in multiple sclerosis. Mashhad University of Medical Sciences 2014-04 /pmc/articles/PMC4046232/ /pubmed/24904717 Text en Copyright: © Journal Management System. Created by sinaweb http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kouchaki, Ebrahim Salehi, Mahdi Reza Sharif, Mohammad Nikoueinejad, Hassan Akbari, Hossein Numerical status of CD4(+)CD25(+)FoxP3(+) and CD8(+)CD28(-) regulatory T cells in multiple sclerosis |
title | Numerical status of CD4(+)CD25(+)FoxP3(+) and CD8(+)CD28(-) regulatory T cells in multiple sclerosis |
title_full | Numerical status of CD4(+)CD25(+)FoxP3(+) and CD8(+)CD28(-) regulatory T cells in multiple sclerosis |
title_fullStr | Numerical status of CD4(+)CD25(+)FoxP3(+) and CD8(+)CD28(-) regulatory T cells in multiple sclerosis |
title_full_unstemmed | Numerical status of CD4(+)CD25(+)FoxP3(+) and CD8(+)CD28(-) regulatory T cells in multiple sclerosis |
title_short | Numerical status of CD4(+)CD25(+)FoxP3(+) and CD8(+)CD28(-) regulatory T cells in multiple sclerosis |
title_sort | numerical status of cd4(+)cd25(+)foxp3(+) and cd8(+)cd28(-) regulatory t cells in multiple sclerosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046232/ https://www.ncbi.nlm.nih.gov/pubmed/24904717 |
work_keys_str_mv | AT kouchakiebrahim numericalstatusofcd4cd25foxp3andcd8cd28regulatorytcellsinmultiplesclerosis AT salehimahdi numericalstatusofcd4cd25foxp3andcd8cd28regulatorytcellsinmultiplesclerosis AT rezasharifmohammad numericalstatusofcd4cd25foxp3andcd8cd28regulatorytcellsinmultiplesclerosis AT nikoueinejadhassan numericalstatusofcd4cd25foxp3andcd8cd28regulatorytcellsinmultiplesclerosis AT akbarihossein numericalstatusofcd4cd25foxp3andcd8cd28regulatorytcellsinmultiplesclerosis |