Hepatitis C Virus Infection and Mixed Cryoglobulinemia

Hepatitis C virus (HCV) chronic infection is recognized as the major cause of mixed cryoglobulinemia (MC). Its persistence represents a continuous stimulus for host immune system with production of circulating immune complexes (ICs), one-third of them with cryoprecipitate property. Several factors c...

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Main Authors: Gianfranco Lauletta, Sabino Russi, Vincenza Conteduca, Loredana Sansonno
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2012/502156
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author Gianfranco Lauletta
Sabino Russi
Vincenza Conteduca
Loredana Sansonno
author_facet Gianfranco Lauletta
Sabino Russi
Vincenza Conteduca
Loredana Sansonno
author_sort Gianfranco Lauletta
collection DOAJ
description Hepatitis C virus (HCV) chronic infection is recognized as the major cause of mixed cryoglobulinemia (MC). Its persistence represents a continuous stimulus for host immune system with production of circulating immune complexes (ICs), one-third of them with cryoprecipitate property. Several factors contribute to the biological activities of ICs, many of which are not completely known. Among them, complement factors play a crucial role in the cold-insoluble ICs-mediated vasculitis, involving primarily small blood vessels in different tissues including skin, kidney, peripheral, and central nervous system. Liver represents the major target of HCV infection with inflammatory infiltrates, resembling secondary lymphoid follicles. Cytokine like CXCL13 contribute to B-cell homing in intraportal lymphoid aggregates, in which B-cell clonal selection may arise. B-cell clonal expansion starts as an antigen-driven event and expands towards indolent and malignant B-cell proliferation. Occurrence of intrahepatic B-cell clonalities correlates with extrahepatic clinical manifestations of HCV infection. In this context, cryoglobulinemic patients should be considered a peculiar HCV-infected population that needs a clinical multidisciplinary approach and more articulated therapeutic measures.
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spelling doaj-art-b0ff90d9843c47b38a54f70af99291332025-02-03T01:23:18ZengWileyClinical and Developmental Immunology1740-25221740-25302012-01-01201210.1155/2012/502156502156Hepatitis C Virus Infection and Mixed CryoglobulinemiaGianfranco Lauletta0Sabino Russi1Vincenza Conteduca2Loredana Sansonno3Department of Biomedical Sciences and Human Oncology, Section of Internal Medicine and Clinical Oncology, Liver Unit, University of Bari Medical School 70124, Bari, ItalyDepartment of Biomedical Sciences and Human Oncology, Section of Internal Medicine and Clinical Oncology, Liver Unit, University of Bari Medical School 70124, Bari, ItalyDepartment of Biomedical Sciences and Human Oncology, Section of Internal Medicine and Clinical Oncology, Liver Unit, University of Bari Medical School 70124, Bari, ItalyDepartment of Biomedical Sciences, University of Foggia, 71122 Foggia, ItalyHepatitis C virus (HCV) chronic infection is recognized as the major cause of mixed cryoglobulinemia (MC). Its persistence represents a continuous stimulus for host immune system with production of circulating immune complexes (ICs), one-third of them with cryoprecipitate property. Several factors contribute to the biological activities of ICs, many of which are not completely known. Among them, complement factors play a crucial role in the cold-insoluble ICs-mediated vasculitis, involving primarily small blood vessels in different tissues including skin, kidney, peripheral, and central nervous system. Liver represents the major target of HCV infection with inflammatory infiltrates, resembling secondary lymphoid follicles. Cytokine like CXCL13 contribute to B-cell homing in intraportal lymphoid aggregates, in which B-cell clonal selection may arise. B-cell clonal expansion starts as an antigen-driven event and expands towards indolent and malignant B-cell proliferation. Occurrence of intrahepatic B-cell clonalities correlates with extrahepatic clinical manifestations of HCV infection. In this context, cryoglobulinemic patients should be considered a peculiar HCV-infected population that needs a clinical multidisciplinary approach and more articulated therapeutic measures.http://dx.doi.org/10.1155/2012/502156
spellingShingle Gianfranco Lauletta
Sabino Russi
Vincenza Conteduca
Loredana Sansonno
Hepatitis C Virus Infection and Mixed Cryoglobulinemia
Clinical and Developmental Immunology
title Hepatitis C Virus Infection and Mixed Cryoglobulinemia
title_full Hepatitis C Virus Infection and Mixed Cryoglobulinemia
title_fullStr Hepatitis C Virus Infection and Mixed Cryoglobulinemia
title_full_unstemmed Hepatitis C Virus Infection and Mixed Cryoglobulinemia
title_short Hepatitis C Virus Infection and Mixed Cryoglobulinemia
title_sort hepatitis c virus infection and mixed cryoglobulinemia
url http://dx.doi.org/10.1155/2012/502156
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AT vincenzaconteduca hepatitiscvirusinfectionandmixedcryoglobulinemia
AT loredanasansonno hepatitiscvirusinfectionandmixedcryoglobulinemia