Cargando…
Autoimmune and Neoplastic Thyroid Diseases Associated with Hepatitis C Chronic Infection
Frequently, patients with hepatitis C virus (HCV) chronic infection have high levels of serum anti-thyroperoxidase and/or anti-thyroglobulin autoantibodies, ultrasonographic signs of chronic autoimmune thyroiditis, and subclinical hypothyroidism, in female gender versus healthy controls, or hepatiti...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211174/ https://www.ncbi.nlm.nih.gov/pubmed/25374602 http://dx.doi.org/10.1155/2014/935131 |
_version_ | 1782341525728919552 |
---|---|
author | Fallahi, Poupak Ferrari, Silvia Martina Politti, Ugo Giuggioli, Dilia Ferri, Clodoveo Antonelli, Alessandro |
author_facet | Fallahi, Poupak Ferrari, Silvia Martina Politti, Ugo Giuggioli, Dilia Ferri, Clodoveo Antonelli, Alessandro |
author_sort | Fallahi, Poupak |
collection | PubMed |
description | Frequently, patients with hepatitis C virus (HCV) chronic infection have high levels of serum anti-thyroperoxidase and/or anti-thyroglobulin autoantibodies, ultrasonographic signs of chronic autoimmune thyroiditis, and subclinical hypothyroidism, in female gender versus healthy controls, or hepatitis B virus infected patients. In patients with “HCV-associated mixed cryoglobulinemia” (MC + HCV), a higher prevalence of thyroid autoimmune disorders was shown not only compared to controls, but also versus HCV patients without cryoglobulinemia. Patients with MC + HCV or HCV chronic infection show a higher prevalence of papillary thyroid cancer than controls, in particular in patients with autoimmune thyroiditis. Patients with HCV chronic infection, or with MC + HCV, in presence of autoimmune thyroiditis, show higher serum levels of T-helper (Th)1 (C-X-C motif) ligand 10 (CXCL10) chemokine, but normal levels of Th2 (C-C motif) ligand 2 chemokine, than patients without thyroiditis. HCV thyroid infection could act by upregulating CXCL10 gene expression and secretion in thyrocytes recruiting Th1 lymphocytes that secrete interferon-γ and tumor necrosis factor-α. These cytokines might induce a further CXCL10 secretion by thyrocytes, thus perpetuating the immune cascade, which may lead to the appearance of autoimmune thyroid disorders in genetically predisposed subjects. A careful monitoring of thyroid function, particularly where nodules occur, is recommended in HCV patients. |
format | Online Article Text |
id | pubmed-4211174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42111742014-11-05 Autoimmune and Neoplastic Thyroid Diseases Associated with Hepatitis C Chronic Infection Fallahi, Poupak Ferrari, Silvia Martina Politti, Ugo Giuggioli, Dilia Ferri, Clodoveo Antonelli, Alessandro Int J Endocrinol Review Article Frequently, patients with hepatitis C virus (HCV) chronic infection have high levels of serum anti-thyroperoxidase and/or anti-thyroglobulin autoantibodies, ultrasonographic signs of chronic autoimmune thyroiditis, and subclinical hypothyroidism, in female gender versus healthy controls, or hepatitis B virus infected patients. In patients with “HCV-associated mixed cryoglobulinemia” (MC + HCV), a higher prevalence of thyroid autoimmune disorders was shown not only compared to controls, but also versus HCV patients without cryoglobulinemia. Patients with MC + HCV or HCV chronic infection show a higher prevalence of papillary thyroid cancer than controls, in particular in patients with autoimmune thyroiditis. Patients with HCV chronic infection, or with MC + HCV, in presence of autoimmune thyroiditis, show higher serum levels of T-helper (Th)1 (C-X-C motif) ligand 10 (CXCL10) chemokine, but normal levels of Th2 (C-C motif) ligand 2 chemokine, than patients without thyroiditis. HCV thyroid infection could act by upregulating CXCL10 gene expression and secretion in thyrocytes recruiting Th1 lymphocytes that secrete interferon-γ and tumor necrosis factor-α. These cytokines might induce a further CXCL10 secretion by thyrocytes, thus perpetuating the immune cascade, which may lead to the appearance of autoimmune thyroid disorders in genetically predisposed subjects. A careful monitoring of thyroid function, particularly where nodules occur, is recommended in HCV patients. Hindawi Publishing Corporation 2014 2014-10-13 /pmc/articles/PMC4211174/ /pubmed/25374602 http://dx.doi.org/10.1155/2014/935131 Text en Copyright © 2014 Poupak Fallahi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Fallahi, Poupak Ferrari, Silvia Martina Politti, Ugo Giuggioli, Dilia Ferri, Clodoveo Antonelli, Alessandro Autoimmune and Neoplastic Thyroid Diseases Associated with Hepatitis C Chronic Infection |
title | Autoimmune and Neoplastic Thyroid Diseases Associated with Hepatitis C Chronic Infection |
title_full | Autoimmune and Neoplastic Thyroid Diseases Associated with Hepatitis C Chronic Infection |
title_fullStr | Autoimmune and Neoplastic Thyroid Diseases Associated with Hepatitis C Chronic Infection |
title_full_unstemmed | Autoimmune and Neoplastic Thyroid Diseases Associated with Hepatitis C Chronic Infection |
title_short | Autoimmune and Neoplastic Thyroid Diseases Associated with Hepatitis C Chronic Infection |
title_sort | autoimmune and neoplastic thyroid diseases associated with hepatitis c chronic infection |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211174/ https://www.ncbi.nlm.nih.gov/pubmed/25374602 http://dx.doi.org/10.1155/2014/935131 |
work_keys_str_mv | AT fallahipoupak autoimmuneandneoplasticthyroiddiseasesassociatedwithhepatitiscchronicinfection AT ferrarisilviamartina autoimmuneandneoplasticthyroiddiseasesassociatedwithhepatitiscchronicinfection AT polittiugo autoimmuneandneoplasticthyroiddiseasesassociatedwithhepatitiscchronicinfection AT giuggiolidilia autoimmuneandneoplasticthyroiddiseasesassociatedwithhepatitiscchronicinfection AT ferriclodoveo autoimmuneandneoplasticthyroiddiseasesassociatedwithhepatitiscchronicinfection AT antonellialessandro autoimmuneandneoplasticthyroiddiseasesassociatedwithhepatitiscchronicinfection |