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Determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets

Background: Thermal burn injuries impair the host defence system. Hence, in the present study, we aimed at investigating the changes in the number and phenotype of peripheral blood lymphocyte populations (T, B, and natural killer cells) and their subpopulations in patients with thermal burns and det...

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Autores principales: Z Entezami, Kobra, Mosavi, Tahere
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iran University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804437/
https://www.ncbi.nlm.nih.gov/pubmed/29445667
http://dx.doi.org/10.14196/mjiri.31.38
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author Z Entezami, Kobra
Mosavi, Tahere
author_facet Z Entezami, Kobra
Mosavi, Tahere
author_sort Z Entezami, Kobra
collection PubMed
description Background: Thermal burn injuries impair the host defence system. Hence, in the present study, we aimed at investigating the changes in the number and phenotype of peripheral blood lymphocyte populations (T, B, and natural killer cells) and their subpopulations in patients with thermal burns and determining the relationships with different sizes of total body surface area (TBSA). Methods: Blood samples from 67 patients, admitted to Motahary Burn Center in Tehran, with burns from 30% to more than 70% TBSA were collected on Days 3 and 7 postburn. Lymphocytes and their subpopulations were identified by monoclonal antibodies. The cells were analyzed using flow cytometry. The results were compared with healthy controls. Results: In this study, 3 and 7 days after burn injury, the percentages of CD3+, CD4+ and CD8+ lymphocyte significantly decreased, CD4+/CD8+ ratios were below the normal range, and CD19+ (B cells) significantly increased. No significant difference was obtained in the mean percentage of CD16+ (NK cells) between Days 3 and 7 postburn. Patients with burns of 30% TBSA or greater (>70%) had a significant reduction in CD3+, CD4+ and CD8+ ( T cells) numbers up to 7 days compared with 3 days after burn injury. Patients with 30% to >70 % TBSA burn failed to show any significant changes in CD4+/CD8+ ratio as well as CD16+ (NK cells) 3 to 7 days after burn. In patients with burns more than 30% to>70% TBSA, CD19+ (B cells) number changes were found to be complicated after 3 and 7 days. Conclusion: The results of this study suggest that alterations of immune cell surface markers and TBSA% can reflect postburn lymphocyte activation.
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spelling pubmed-58044372018-02-14 Determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets Z Entezami, Kobra Mosavi, Tahere Med J Islam Repub Iran Original Article Background: Thermal burn injuries impair the host defence system. Hence, in the present study, we aimed at investigating the changes in the number and phenotype of peripheral blood lymphocyte populations (T, B, and natural killer cells) and their subpopulations in patients with thermal burns and determining the relationships with different sizes of total body surface area (TBSA). Methods: Blood samples from 67 patients, admitted to Motahary Burn Center in Tehran, with burns from 30% to more than 70% TBSA were collected on Days 3 and 7 postburn. Lymphocytes and their subpopulations were identified by monoclonal antibodies. The cells were analyzed using flow cytometry. The results were compared with healthy controls. Results: In this study, 3 and 7 days after burn injury, the percentages of CD3+, CD4+ and CD8+ lymphocyte significantly decreased, CD4+/CD8+ ratios were below the normal range, and CD19+ (B cells) significantly increased. No significant difference was obtained in the mean percentage of CD16+ (NK cells) between Days 3 and 7 postburn. Patients with burns of 30% TBSA or greater (>70%) had a significant reduction in CD3+, CD4+ and CD8+ ( T cells) numbers up to 7 days compared with 3 days after burn injury. Patients with 30% to >70 % TBSA burn failed to show any significant changes in CD4+/CD8+ ratio as well as CD16+ (NK cells) 3 to 7 days after burn. In patients with burns more than 30% to>70% TBSA, CD19+ (B cells) number changes were found to be complicated after 3 and 7 days. Conclusion: The results of this study suggest that alterations of immune cell surface markers and TBSA% can reflect postburn lymphocyte activation. Iran University of Medical Sciences 2017-07-15 /pmc/articles/PMC5804437/ /pubmed/29445667 http://dx.doi.org/10.14196/mjiri.31.38 Text en © 2017 Iran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Z Entezami, Kobra
Mosavi, Tahere
Determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets
title Determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets
title_full Determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets
title_fullStr Determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets
title_full_unstemmed Determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets
title_short Determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets
title_sort determination of lymphocytes surface markers in patients with thermal burns and the influence of burn size on mononuclear cell subsets
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804437/
https://www.ncbi.nlm.nih.gov/pubmed/29445667
http://dx.doi.org/10.14196/mjiri.31.38
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