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Association of C-type lectin 18 levels with extrahepatic manifestations in chronic HCV infection

Mixed cryobulinemia (MC) is the most common chronic hepatitis C virus (HCV)-associated extrahepatic manifestation. C-type lectin 18 (CLEC18) is a novel secretory lectin that is abundantly expressed in hepatocytes and peripheral blood cells (PBCs). We investigated the associations between CLEC18 expr...

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Autores principales: Liao, Tsai-Ling, Huang, Ya-Lang, Chen, Yi-Ming, Lee, Hsiu-Chin, Chen, Der-Yuan, Hsieh, Shie-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251874/
https://www.ncbi.nlm.nih.gov/pubmed/30470801
http://dx.doi.org/10.1038/s41598-018-35774-w
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author Liao, Tsai-Ling
Huang, Ya-Lang
Chen, Yi-Ming
Lee, Hsiu-Chin
Chen, Der-Yuan
Hsieh, Shie-Liang
author_facet Liao, Tsai-Ling
Huang, Ya-Lang
Chen, Yi-Ming
Lee, Hsiu-Chin
Chen, Der-Yuan
Hsieh, Shie-Liang
author_sort Liao, Tsai-Ling
collection PubMed
description Mixed cryobulinemia (MC) is the most common chronic hepatitis C virus (HCV)-associated extrahepatic manifestation. C-type lectin 18 (CLEC18) is a novel secretory lectin that is abundantly expressed in hepatocytes and peripheral blood cells (PBCs). We investigated the associations between CLEC18 expression during HCV infection and the presence of extrahepatic manifestations. A total of 41 rheumatic patients with HCV infection (including 28 patients with MC syndrome), 45 rheumatic patients without infection, and 14 healthy subjects were enrolled. The CLEC18 levels in PBCs and serum were determined by using flow cytometry and enzyme-linked immunosorbent assay, respectively. Significantly higher CLEC18 levels were observed in patients with HCV infection (P < 0.001) and were positively correlated with HCV viral loads (γ = 0.56, P < 0.05). Among patients with HCV infection, significantly increased CLEC18 levels were observed in patients with MC syndrome, particularly in those with type II MC (P < 0.05). CLEC18 levels were associated with cryoglobulin and C4 levels (P < 0.05). CLEC18 was significantly associated with HCV infection, particularly in those with HCV-associated MC. CLEC18 levels were also positively correlated with MC disease activity, suggesting its involvement in MC pathogenesis. CLEC18 may be a novel indicator of HCV infection and a potential therapeutic target in rheumatic patients.
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spelling pubmed-62518742018-11-29 Association of C-type lectin 18 levels with extrahepatic manifestations in chronic HCV infection Liao, Tsai-Ling Huang, Ya-Lang Chen, Yi-Ming Lee, Hsiu-Chin Chen, Der-Yuan Hsieh, Shie-Liang Sci Rep Article Mixed cryobulinemia (MC) is the most common chronic hepatitis C virus (HCV)-associated extrahepatic manifestation. C-type lectin 18 (CLEC18) is a novel secretory lectin that is abundantly expressed in hepatocytes and peripheral blood cells (PBCs). We investigated the associations between CLEC18 expression during HCV infection and the presence of extrahepatic manifestations. A total of 41 rheumatic patients with HCV infection (including 28 patients with MC syndrome), 45 rheumatic patients without infection, and 14 healthy subjects were enrolled. The CLEC18 levels in PBCs and serum were determined by using flow cytometry and enzyme-linked immunosorbent assay, respectively. Significantly higher CLEC18 levels were observed in patients with HCV infection (P < 0.001) and were positively correlated with HCV viral loads (γ = 0.56, P < 0.05). Among patients with HCV infection, significantly increased CLEC18 levels were observed in patients with MC syndrome, particularly in those with type II MC (P < 0.05). CLEC18 levels were associated with cryoglobulin and C4 levels (P < 0.05). CLEC18 was significantly associated with HCV infection, particularly in those with HCV-associated MC. CLEC18 levels were also positively correlated with MC disease activity, suggesting its involvement in MC pathogenesis. CLEC18 may be a novel indicator of HCV infection and a potential therapeutic target in rheumatic patients. Nature Publishing Group UK 2018-11-23 /pmc/articles/PMC6251874/ /pubmed/30470801 http://dx.doi.org/10.1038/s41598-018-35774-w Text en © The Author(s) 2018 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
Liao, Tsai-Ling
Huang, Ya-Lang
Chen, Yi-Ming
Lee, Hsiu-Chin
Chen, Der-Yuan
Hsieh, Shie-Liang
Association of C-type lectin 18 levels with extrahepatic manifestations in chronic HCV infection
title Association of C-type lectin 18 levels with extrahepatic manifestations in chronic HCV infection
title_full Association of C-type lectin 18 levels with extrahepatic manifestations in chronic HCV infection
title_fullStr Association of C-type lectin 18 levels with extrahepatic manifestations in chronic HCV infection
title_full_unstemmed Association of C-type lectin 18 levels with extrahepatic manifestations in chronic HCV infection
title_short Association of C-type lectin 18 levels with extrahepatic manifestations in chronic HCV infection
title_sort association of c-type lectin 18 levels with extrahepatic manifestations in chronic hcv infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251874/
https://www.ncbi.nlm.nih.gov/pubmed/30470801
http://dx.doi.org/10.1038/s41598-018-35774-w
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