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Identification of circulating monocytes as producers of tuberculosis disease biomarker C1q
Tuberculosis (TB) is a prevalent disease causing an estimated 1.6 million deaths and 10.6 million new cases annually. Discriminating TB disease from differential diagnoses can be complex, particularly in the field. Increased levels of complement component C1q in serum have been identified as a speci...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354225/ https://www.ncbi.nlm.nih.gov/pubmed/37464009 http://dx.doi.org/10.1038/s41598-023-38889-x |
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author | Niewold, Paula Dijkstra, Douwe J. Cai, Yi Goletti, Delia Palmieri, Fabrizio van Meijgaarden, Krista E. Verreck, Frank A. W. Akkerman, Onno W. Hofland, Regina W. Delemarre, Eveline M. Nierkens, Stefan Verheul, Marije K. Pollard, Andrew J. van Dissel, Jaap T. Ottenhoff, Tom H. M. Trouw, Leendert A. Joosten, Simone A. |
author_facet | Niewold, Paula Dijkstra, Douwe J. Cai, Yi Goletti, Delia Palmieri, Fabrizio van Meijgaarden, Krista E. Verreck, Frank A. W. Akkerman, Onno W. Hofland, Regina W. Delemarre, Eveline M. Nierkens, Stefan Verheul, Marije K. Pollard, Andrew J. van Dissel, Jaap T. Ottenhoff, Tom H. M. Trouw, Leendert A. Joosten, Simone A. |
author_sort | Niewold, Paula |
collection | PubMed |
description | Tuberculosis (TB) is a prevalent disease causing an estimated 1.6 million deaths and 10.6 million new cases annually. Discriminating TB disease from differential diagnoses can be complex, particularly in the field. Increased levels of complement component C1q in serum have been identified as a specific and accessible biomarker for TB disease but the source of C1q in circulation has not been identified. Here, data and samples previously collected from human cohorts, a clinical trial and a non-human primate study were used to identify cells producing C1q in circulation. Cell subset frequencies were correlated with serum C1q levels and combined with single cell RNA sequencing and flow cytometry analyses. This identified monocytes as C1q producers in circulation, with a pronounced expression of C1q in classical and intermediate monocytes and variable expression in non-classical monocytes. |
format | Online Article Text |
id | pubmed-10354225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103542252023-07-20 Identification of circulating monocytes as producers of tuberculosis disease biomarker C1q Niewold, Paula Dijkstra, Douwe J. Cai, Yi Goletti, Delia Palmieri, Fabrizio van Meijgaarden, Krista E. Verreck, Frank A. W. Akkerman, Onno W. Hofland, Regina W. Delemarre, Eveline M. Nierkens, Stefan Verheul, Marije K. Pollard, Andrew J. van Dissel, Jaap T. Ottenhoff, Tom H. M. Trouw, Leendert A. Joosten, Simone A. Sci Rep Article Tuberculosis (TB) is a prevalent disease causing an estimated 1.6 million deaths and 10.6 million new cases annually. Discriminating TB disease from differential diagnoses can be complex, particularly in the field. Increased levels of complement component C1q in serum have been identified as a specific and accessible biomarker for TB disease but the source of C1q in circulation has not been identified. Here, data and samples previously collected from human cohorts, a clinical trial and a non-human primate study were used to identify cells producing C1q in circulation. Cell subset frequencies were correlated with serum C1q levels and combined with single cell RNA sequencing and flow cytometry analyses. This identified monocytes as C1q producers in circulation, with a pronounced expression of C1q in classical and intermediate monocytes and variable expression in non-classical monocytes. Nature Publishing Group UK 2023-07-18 /pmc/articles/PMC10354225/ /pubmed/37464009 http://dx.doi.org/10.1038/s41598-023-38889-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Niewold, Paula Dijkstra, Douwe J. Cai, Yi Goletti, Delia Palmieri, Fabrizio van Meijgaarden, Krista E. Verreck, Frank A. W. Akkerman, Onno W. Hofland, Regina W. Delemarre, Eveline M. Nierkens, Stefan Verheul, Marije K. Pollard, Andrew J. van Dissel, Jaap T. Ottenhoff, Tom H. M. Trouw, Leendert A. Joosten, Simone A. Identification of circulating monocytes as producers of tuberculosis disease biomarker C1q |
title | Identification of circulating monocytes as producers of tuberculosis disease biomarker C1q |
title_full | Identification of circulating monocytes as producers of tuberculosis disease biomarker C1q |
title_fullStr | Identification of circulating monocytes as producers of tuberculosis disease biomarker C1q |
title_full_unstemmed | Identification of circulating monocytes as producers of tuberculosis disease biomarker C1q |
title_short | Identification of circulating monocytes as producers of tuberculosis disease biomarker C1q |
title_sort | identification of circulating monocytes as producers of tuberculosis disease biomarker c1q |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354225/ https://www.ncbi.nlm.nih.gov/pubmed/37464009 http://dx.doi.org/10.1038/s41598-023-38889-x |
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