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Effects of Beryllium on Human Serum Immunoglobulin and Lymphocyte Subpopulation
To investigate the effects of short-term exposure of beryllium on the human immune system, the proportion of T-lymphocytes such as CD3+, CD4+, CD8+, CD95, and NK cells, andthe proportion of B cells and TNFα level in peripheral blood and immunoglobulins in the serum of 43 exposed workers and 34 healt...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Toxicology
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834450/ https://www.ncbi.nlm.nih.gov/pubmed/24278637 http://dx.doi.org/10.5487/TR.2013.29.2.115 |
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author | Kim, Ki-Woong Kim, DaeSeong Won, Yong Lim Kang, Seong-Kyu |
author_facet | Kim, Ki-Woong Kim, DaeSeong Won, Yong Lim Kang, Seong-Kyu |
author_sort | Kim, Ki-Woong |
collection | PubMed |
description | To investigate the effects of short-term exposure of beryllium on the human immune system, the proportion of T-lymphocytes such as CD3+, CD4+, CD8+, CD95, and NK cells, andthe proportion of B cells and TNFα level in peripheral blood and immunoglobulins in the serum of 43 exposed workers and 34 healthy control subjects were studied. External exposure to beryllium was measured by atomic absorption spectrometer as recommended by the NIOSH analytical method 7300. T lymphocyte subpopulation analysis was carried out with flow cytometer. The working duration of exposed workers was less than 3 months and the mean ambient beryllium level was 3.4 μg/m(3), 112.3 μg/m(3), and 2.3 μg/m(3) in molding (furnace), deforming (grinding), and sorting processes, respectively (cited from Kim et al., 2008). However, ambient beryllium level after process change was non-detectable (< 0.1 μg/m(3)). The number of T lymphocytes and the amount of immunoglobulins in the beryllium-exposed workers and control subjects were not significantly different, except for the total number of lymphocytes and CD95 (APO1/FAS). The total number of lymphocytes was higher in the beryllium-exposed individuals than in the healthy control subjects. Multiple logistic regression analysis showed lymphocytes to be affected by beryllium exposure (odd ratio = 7.293; p < 0.001). These results show that short-term exposure to beryllium does not induce immune dysfunction but is probably associated with lymphocytes proliferation. |
format | Online Article Text |
id | pubmed-3834450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Korean Society of Toxicology |
record_format | MEDLINE/PubMed |
spelling | pubmed-38344502013-11-25 Effects of Beryllium on Human Serum Immunoglobulin and Lymphocyte Subpopulation Kim, Ki-Woong Kim, DaeSeong Won, Yong Lim Kang, Seong-Kyu Toxicol Res Articles To investigate the effects of short-term exposure of beryllium on the human immune system, the proportion of T-lymphocytes such as CD3+, CD4+, CD8+, CD95, and NK cells, andthe proportion of B cells and TNFα level in peripheral blood and immunoglobulins in the serum of 43 exposed workers and 34 healthy control subjects were studied. External exposure to beryllium was measured by atomic absorption spectrometer as recommended by the NIOSH analytical method 7300. T lymphocyte subpopulation analysis was carried out with flow cytometer. The working duration of exposed workers was less than 3 months and the mean ambient beryllium level was 3.4 μg/m(3), 112.3 μg/m(3), and 2.3 μg/m(3) in molding (furnace), deforming (grinding), and sorting processes, respectively (cited from Kim et al., 2008). However, ambient beryllium level after process change was non-detectable (< 0.1 μg/m(3)). The number of T lymphocytes and the amount of immunoglobulins in the beryllium-exposed workers and control subjects were not significantly different, except for the total number of lymphocytes and CD95 (APO1/FAS). The total number of lymphocytes was higher in the beryllium-exposed individuals than in the healthy control subjects. Multiple logistic regression analysis showed lymphocytes to be affected by beryllium exposure (odd ratio = 7.293; p < 0.001). These results show that short-term exposure to beryllium does not induce immune dysfunction but is probably associated with lymphocytes proliferation. The Korean Society of Toxicology 2013-06 /pmc/articles/PMC3834450/ /pubmed/24278637 http://dx.doi.org/10.5487/TR.2013.29.2.115 Text en Copyright ©2013, The Korean Society of Toxicology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http:// creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Kim, Ki-Woong Kim, DaeSeong Won, Yong Lim Kang, Seong-Kyu Effects of Beryllium on Human Serum Immunoglobulin and Lymphocyte Subpopulation |
title | Effects of Beryllium on Human Serum Immunoglobulin and Lymphocyte Subpopulation |
title_full | Effects of Beryllium on Human Serum Immunoglobulin and Lymphocyte Subpopulation |
title_fullStr | Effects of Beryllium on Human Serum Immunoglobulin and Lymphocyte Subpopulation |
title_full_unstemmed | Effects of Beryllium on Human Serum Immunoglobulin and Lymphocyte Subpopulation |
title_short | Effects of Beryllium on Human Serum Immunoglobulin and Lymphocyte Subpopulation |
title_sort | effects of beryllium on human serum immunoglobulin and lymphocyte subpopulation |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834450/ https://www.ncbi.nlm.nih.gov/pubmed/24278637 http://dx.doi.org/10.5487/TR.2013.29.2.115 |
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