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Published on: September 25, 2019
Polyclonal and monoclonal B lymphocytes response in HCV-infected patients treated with direct-acting antiviral agents
A Schiavinato1, A Zanetto2, G Pantano1
1Department of Laboratory Medicine, University-Hospital of Padova, Padova, Italy.
Insights
Interferon-free antiviral treatment significantly reduced B cells in Hepatitis C virus (HCV)-infected patients with lymphoproliferative disorders. However, some monoclonal B cell populations persisted after viral eradication, indicating ongoing disease risk.
Area of Science:
- Hepatology
- Immunology
- Virology
Background:
- Chronic Hepatitis C virus (HCV) infection is linked to serious extrahepatic manifestations like lymphoproliferative disorders.
- These conditions increase morbidity and mortality rates in HCV patients.
Purpose of the Study:
- To assess the impact of interferon-free antiviral therapy on peripheral blood lymphocytes in HCV patients.
- To evaluate changes in B-cell populations and immunoglobulin light chain ratios in patients with and without lymphoproliferative disorders.
Main Methods:
- Flow cytometry was used to analyze peripheral blood lymphocytes before and after treatment.
- Immunoglobulin (Ig) light chain κ/λ ratio was monitored in patients with lymphoproliferative disorders.
- HCV-infected patients and healthy volunteers were included in the study.
Main Results:
- All 29 patients achieved sustained virological response.
- A significant 39% reduction in the B-cell compartment was observed in 8 of 9 HCV patients with lymphoproliferative disorders.
- While 3 patients showed normalization of Ig light chain ratios, 6 patients still had persistent monoclonal B cells a year post-treatment.
Conclusions:
- Direct-acting antiviral (DAA) treatment effectively reduces pathological B cells in HCV patients with associated lymphoproliferative disorders.
- Despite viral eradication, monoclonal B cell populations can persist, suggesting a need for continued monitoring.
Abstract:
Hepatitis C virus (HCV) chronic infection can be associated with extrahepatic manifestations such as mixed cryoglobulinaemia and lymphoproliferative disorders that are endowed with increased rates of morbidity and all-cause mortality. In this study, we used flow cytometry to evaluate the effect of interferon-free antiviral treatment on peripheral blood lymphocytes in HCV-infected patients with or without associated lymphoproliferative disorders. Flow cytometry analysis of peripheral blood lymphocytes was performed at baseline and at the end of treatment. In HCV-infected patients with lymphoproliferative disorders, we evaluated immunoglobulin (Ig) light chain κ/λ ratio variations as a measure of monoclonal B-cell response to antiviral therapy. Healthy volunteers were enrolled as controls. A total of 29 patients were included, nine with and 20 without lymphoproliferative disorders. Sustained virological response was achieved in 29 of 29 patients. We observed a significant reduction in the B-cell compartment (39% global reduction) in eight of nine HCV-infected patients with lymphoproliferative disorders after viral clearance. We recognized the same trend, even if less pronounced, in HCV-infected patients without lymphoproliferative disorders (9% global reduction). Among HCV-infected patients with lymphoproliferative disorders, three showed an improvement/normalization of the immunoglobulin light chain ratio, whereas in the remaining six patients monoclonal B cells persisted to be clonally restricted even 1 year after the end of treatment. Our data show that DAAs treatment can be effective in reducing the frequency of pathological B cells in the peripheral blood of HCV-infected patients affected by HCV-associated lymphoproliferative disorders; however, monoclonal populations can persist after viral eradication.
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