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Leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis
Tuberculosis (TB) caused by Mycobacterium tuberculosis (Mtb) is a global health problem. At present, prior exposure to Mtb can be determined by blood-based interferon-gamma release assay (IGRA), but active TB is not always detectable by blood tests such as CRP and ESR. This study was undertaken to i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7042324/ https://www.ncbi.nlm.nih.gov/pubmed/32099022 http://dx.doi.org/10.1038/s41598-020-60450-3 |
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author | Fujimoto, Minoru Matsumoto, Tomoshige Serada, Satoshi Tsujimura, Yusuke Hashimoto, Shoji Yasutomi, Yasuhiro Naka, Tetsuji |
author_facet | Fujimoto, Minoru Matsumoto, Tomoshige Serada, Satoshi Tsujimura, Yusuke Hashimoto, Shoji Yasutomi, Yasuhiro Naka, Tetsuji |
author_sort | Fujimoto, Minoru |
collection | PubMed |
description | Tuberculosis (TB) caused by Mycobacterium tuberculosis (Mtb) is a global health problem. At present, prior exposure to Mtb can be determined by blood-based interferon-gamma release assay (IGRA), but active TB is not always detectable by blood tests such as CRP and ESR. This study was undertaken to investigate whether leucine-rich alpha-2 glycoprotein (LRG), a new inflammatory biomarker, could be used to assess active disease of TB. Cynomolgus macaques pretreated with or without Bacille Calmette-Guerin (BCG) vaccination were inoculated with Mtb to induce active TB. Blood was collected over time from these animals and levels of LRG as well as CRP and ESR were quantified. In the macaques without BCG vaccination, Mtb inoculation caused extensive TB and significantly increased plasma CRP and LRG levels, but not ESR. In the macaques with BCG vaccination, whereas Mtb challenge caused pulmonary TB, only LRG levels were significantly elevated. By immunohistochemical analysis of the lung, LRG was visualized in epithelioid cells and giant cells of the granulation tissue. In humans, serum LRG levels in TB patients were significantly higher than those in healthy controls and declined one month after anti-tubercular therapy. These findings suggest that LRG is a promising biomarker when performed following IGRA for the detection of active TB. |
format | Online Article Text |
id | pubmed-7042324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70423242020-03-03 Leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis Fujimoto, Minoru Matsumoto, Tomoshige Serada, Satoshi Tsujimura, Yusuke Hashimoto, Shoji Yasutomi, Yasuhiro Naka, Tetsuji Sci Rep Article Tuberculosis (TB) caused by Mycobacterium tuberculosis (Mtb) is a global health problem. At present, prior exposure to Mtb can be determined by blood-based interferon-gamma release assay (IGRA), but active TB is not always detectable by blood tests such as CRP and ESR. This study was undertaken to investigate whether leucine-rich alpha-2 glycoprotein (LRG), a new inflammatory biomarker, could be used to assess active disease of TB. Cynomolgus macaques pretreated with or without Bacille Calmette-Guerin (BCG) vaccination were inoculated with Mtb to induce active TB. Blood was collected over time from these animals and levels of LRG as well as CRP and ESR were quantified. In the macaques without BCG vaccination, Mtb inoculation caused extensive TB and significantly increased plasma CRP and LRG levels, but not ESR. In the macaques with BCG vaccination, whereas Mtb challenge caused pulmonary TB, only LRG levels were significantly elevated. By immunohistochemical analysis of the lung, LRG was visualized in epithelioid cells and giant cells of the granulation tissue. In humans, serum LRG levels in TB patients were significantly higher than those in healthy controls and declined one month after anti-tubercular therapy. These findings suggest that LRG is a promising biomarker when performed following IGRA for the detection of active TB. Nature Publishing Group UK 2020-02-25 /pmc/articles/PMC7042324/ /pubmed/32099022 http://dx.doi.org/10.1038/s41598-020-60450-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fujimoto, Minoru Matsumoto, Tomoshige Serada, Satoshi Tsujimura, Yusuke Hashimoto, Shoji Yasutomi, Yasuhiro Naka, Tetsuji Leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis |
title | Leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis |
title_full | Leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis |
title_fullStr | Leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis |
title_full_unstemmed | Leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis |
title_short | Leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis |
title_sort | leucine-rich alpha 2 glycoprotein is a new marker for active disease of tuberculosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7042324/ https://www.ncbi.nlm.nih.gov/pubmed/32099022 http://dx.doi.org/10.1038/s41598-020-60450-3 |
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