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Serum Levels of Soluble Interleukin-2 Receptor in Pulmonary Tuberculosis

It is well known that the activation of cell mediated immunity has an important role in the pathogenesis of pulmonary tuberculosis and the production of the protective immunity against Mycobacterium tuberculosis. During the activation of T-cell by Interleukin-1 released from the macrophage, not only...

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Autores principales: Choi, Soo Jeon, Moon, Young Soo, Lee, Bong Choon, Kim, Dong Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534993/
https://www.ncbi.nlm.nih.gov/pubmed/2271510
http://dx.doi.org/10.3904/kjim.1990.5.1.44
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author Choi, Soo Jeon
Moon, Young Soo
Lee, Bong Choon
Kim, Dong Soon
author_facet Choi, Soo Jeon
Moon, Young Soo
Lee, Bong Choon
Kim, Dong Soon
author_sort Choi, Soo Jeon
collection PubMed
description It is well known that the activation of cell mediated immunity has an important role in the pathogenesis of pulmonary tuberculosis and the production of the protective immunity against Mycobacterium tuberculosis. During the activation of T-cell by Interleukin-1 released from the macrophage, not only Interleukin-2 but also the soluble Interleukin-2 receptor (sIL-2R) molecule is released into the extracellular fluid. In vitro study reveals that the level of this sIL-2R is well correlated with the degree of activation of the T-cell. We therefore carried out this study to evaluate the significance of the serum IL-2R level in determining the disease activity of pulmonary tuberculosis. The level of SIL-2R was measured by sandwich ELISA method. The level of sIL-2R in 42 patients with bacteriologically -proven active pulmonary tuberculosis (29 far and moderately advanced pulmonary tuberculosis, age: 30.3 ±10.3 yrs; 13 minimal pulmonary tuberculosis, age: 34.4 ± 15.3 yrs) was 1111 ± 424 u/ml, which was significantly higher than the normal control group (age: 31.0±9.9 yrs) (365±143 u/ml) and inactive pulmonary tuberculosis group (age: 37.3 ± 16.9 yrs) (465 ± 131 u/ml). But there was no significant difference between 29 patients with advanced pulmonary tuberculosis (1138 ± 405 u/ml) and 13 patients with minimal pulmonary tuberculosis (1051 ± 474 u/ml). More than three months after the initiation of antituberculosis chemotherapy, the follow-up level of serum sIL-2R in 21 patients with active pulmonary tuberculosis (advanced pulmonary tuberculosis 15, minimal pulmonary tuberculosis six) was 533 ± 182 u/ml, which was markedly lower than the pretreatment level (1020 ± 323 u/ml). In conclusion, the high level of sIL-2R (especially over 1000 u/ml) can be used as a marker of disease activity in pulmonary tuberculosis even though not diagnostic.
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spelling pubmed-45349932015-10-02 Serum Levels of Soluble Interleukin-2 Receptor in Pulmonary Tuberculosis Choi, Soo Jeon Moon, Young Soo Lee, Bong Choon Kim, Dong Soon Korean J Intern Med Original Article It is well known that the activation of cell mediated immunity has an important role in the pathogenesis of pulmonary tuberculosis and the production of the protective immunity against Mycobacterium tuberculosis. During the activation of T-cell by Interleukin-1 released from the macrophage, not only Interleukin-2 but also the soluble Interleukin-2 receptor (sIL-2R) molecule is released into the extracellular fluid. In vitro study reveals that the level of this sIL-2R is well correlated with the degree of activation of the T-cell. We therefore carried out this study to evaluate the significance of the serum IL-2R level in determining the disease activity of pulmonary tuberculosis. The level of SIL-2R was measured by sandwich ELISA method. The level of sIL-2R in 42 patients with bacteriologically -proven active pulmonary tuberculosis (29 far and moderately advanced pulmonary tuberculosis, age: 30.3 ±10.3 yrs; 13 minimal pulmonary tuberculosis, age: 34.4 ± 15.3 yrs) was 1111 ± 424 u/ml, which was significantly higher than the normal control group (age: 31.0±9.9 yrs) (365±143 u/ml) and inactive pulmonary tuberculosis group (age: 37.3 ± 16.9 yrs) (465 ± 131 u/ml). But there was no significant difference between 29 patients with advanced pulmonary tuberculosis (1138 ± 405 u/ml) and 13 patients with minimal pulmonary tuberculosis (1051 ± 474 u/ml). More than three months after the initiation of antituberculosis chemotherapy, the follow-up level of serum sIL-2R in 21 patients with active pulmonary tuberculosis (advanced pulmonary tuberculosis 15, minimal pulmonary tuberculosis six) was 533 ± 182 u/ml, which was markedly lower than the pretreatment level (1020 ± 323 u/ml). In conclusion, the high level of sIL-2R (especially over 1000 u/ml) can be used as a marker of disease activity in pulmonary tuberculosis even though not diagnostic. Korean Association of Internal Medicine 1990-01 /pmc/articles/PMC4534993/ /pubmed/2271510 http://dx.doi.org/10.3904/kjim.1990.5.1.44 Text en Copyright © 1990 The Korean Association of Internal Medicine 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 noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Soo Jeon
Moon, Young Soo
Lee, Bong Choon
Kim, Dong Soon
Serum Levels of Soluble Interleukin-2 Receptor in Pulmonary Tuberculosis
title Serum Levels of Soluble Interleukin-2 Receptor in Pulmonary Tuberculosis
title_full Serum Levels of Soluble Interleukin-2 Receptor in Pulmonary Tuberculosis
title_fullStr Serum Levels of Soluble Interleukin-2 Receptor in Pulmonary Tuberculosis
title_full_unstemmed Serum Levels of Soluble Interleukin-2 Receptor in Pulmonary Tuberculosis
title_short Serum Levels of Soluble Interleukin-2 Receptor in Pulmonary Tuberculosis
title_sort serum levels of soluble interleukin-2 receptor in pulmonary tuberculosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534993/
https://www.ncbi.nlm.nih.gov/pubmed/2271510
http://dx.doi.org/10.3904/kjim.1990.5.1.44
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