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The association of semaphorins 3C, 5A and 6D with liver fibrosis stage in chronic hepatitis C
Semaphorins are a diverse family of immunoregulators recently recognized to play a major role in various phases of immune responses. Their role in chronic viral hepatitis C (CHC) and contribution to the progression of liver disease is unknown. The aim of this study was to analyse the association of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310274/ https://www.ncbi.nlm.nih.gov/pubmed/30592759 http://dx.doi.org/10.1371/journal.pone.0209481 |
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author | Papic, Neven Zidovec Lepej, Snjezana Gorenec, Lana Grgic, Ivana Gasparov, Slavko Filipec Kanizaj, Tajana Vince, Adriana |
author_facet | Papic, Neven Zidovec Lepej, Snjezana Gorenec, Lana Grgic, Ivana Gasparov, Slavko Filipec Kanizaj, Tajana Vince, Adriana |
author_sort | Papic, Neven |
collection | PubMed |
description | Semaphorins are a diverse family of immunoregulators recently recognized to play a major role in various phases of immune responses. Their role in chronic viral hepatitis C (CHC) and contribution to the progression of liver disease is unknown. The aim of this study was to analyse the association of secreted semaphorins with the severity of liver disease in patients with CHC. Serum concentrations of semaphorins were measured in 114 treatment-naive CHC patients and 36 healthy controls. Serum concentrations of SEMA3A, SEMA3C, SEMA5A, SEMA6B and SEMA6D were significantly increased in patients with CHC compared to controls. While serum concentrations of SEMA3C and SEMA6D significantly increased with fibrosis stage in both HCV-g1 and HCV-g3 infections, the concentration of SEMA5A inversely correlated with fibrosis stage in both HCV genotypes. ROC analysis showed that serum concentrations of SEMA3C (>4.0ng/mL, AUC 0.88) and SEMA6D (>4.5, AUC 0.82) had higher AUC than widely used APRI (AUC 0.71) and FIB-4 (AUC 0.74) scores. Serum concentrations of SEMA3C and SEMA6D significantly decreased after DAA and PEG IFN-α/ribavirin therapy, while the serum concentration of SEMA5A significantly increased after DAAs therapy. Immunohistochemistry confirmed the expression of SEMA3C and SEMA5A in hepatocytes, endothelial cells and lymphocytes of cirrhotic livers from CHC patients but not in controls. In conclusion, we provide the first evidence that SEMA3C, SEMA5A and SEMA6D can be considered as markers of liver injury in CHC. |
format | Online Article Text |
id | pubmed-6310274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-63102742019-01-08 The association of semaphorins 3C, 5A and 6D with liver fibrosis stage in chronic hepatitis C Papic, Neven Zidovec Lepej, Snjezana Gorenec, Lana Grgic, Ivana Gasparov, Slavko Filipec Kanizaj, Tajana Vince, Adriana PLoS One Research Article Semaphorins are a diverse family of immunoregulators recently recognized to play a major role in various phases of immune responses. Their role in chronic viral hepatitis C (CHC) and contribution to the progression of liver disease is unknown. The aim of this study was to analyse the association of secreted semaphorins with the severity of liver disease in patients with CHC. Serum concentrations of semaphorins were measured in 114 treatment-naive CHC patients and 36 healthy controls. Serum concentrations of SEMA3A, SEMA3C, SEMA5A, SEMA6B and SEMA6D were significantly increased in patients with CHC compared to controls. While serum concentrations of SEMA3C and SEMA6D significantly increased with fibrosis stage in both HCV-g1 and HCV-g3 infections, the concentration of SEMA5A inversely correlated with fibrosis stage in both HCV genotypes. ROC analysis showed that serum concentrations of SEMA3C (>4.0ng/mL, AUC 0.88) and SEMA6D (>4.5, AUC 0.82) had higher AUC than widely used APRI (AUC 0.71) and FIB-4 (AUC 0.74) scores. Serum concentrations of SEMA3C and SEMA6D significantly decreased after DAA and PEG IFN-α/ribavirin therapy, while the serum concentration of SEMA5A significantly increased after DAAs therapy. Immunohistochemistry confirmed the expression of SEMA3C and SEMA5A in hepatocytes, endothelial cells and lymphocytes of cirrhotic livers from CHC patients but not in controls. In conclusion, we provide the first evidence that SEMA3C, SEMA5A and SEMA6D can be considered as markers of liver injury in CHC. Public Library of Science 2018-12-28 /pmc/articles/PMC6310274/ /pubmed/30592759 http://dx.doi.org/10.1371/journal.pone.0209481 Text en © 2018 Papic et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Papic, Neven Zidovec Lepej, Snjezana Gorenec, Lana Grgic, Ivana Gasparov, Slavko Filipec Kanizaj, Tajana Vince, Adriana The association of semaphorins 3C, 5A and 6D with liver fibrosis stage in chronic hepatitis C |
title | The association of semaphorins 3C, 5A and 6D with liver fibrosis stage in chronic hepatitis C |
title_full | The association of semaphorins 3C, 5A and 6D with liver fibrosis stage in chronic hepatitis C |
title_fullStr | The association of semaphorins 3C, 5A and 6D with liver fibrosis stage in chronic hepatitis C |
title_full_unstemmed | The association of semaphorins 3C, 5A and 6D with liver fibrosis stage in chronic hepatitis C |
title_short | The association of semaphorins 3C, 5A and 6D with liver fibrosis stage in chronic hepatitis C |
title_sort | association of semaphorins 3c, 5a and 6d with liver fibrosis stage in chronic hepatitis c |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310274/ https://www.ncbi.nlm.nih.gov/pubmed/30592759 http://dx.doi.org/10.1371/journal.pone.0209481 |
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