Related Experiment Video
Updated: Dec 8, 2025

Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
Published on: September 25, 2019
Successful DAA therapy for chronic hepatitis C reduces HLA-DR on monocytes and circulating immune mediators: A
Natalia Fonseca Rosário1, Geórgia do Nascimento Saraiva1, Thalia Medeiros1
1Laboratório Multiusuário de Apoio à Pesquisa em Nefrologia e Ciências Médicas, Faculdade de Medicina, Hospital Universitário Antônio Pedro, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Insights
Direct-acting antiviral (DAA) treatment for hepatitis C (HCV) eradicated the virus but did not alter monocyte subsets. Long-term, DAA therapy reduced monocyte activation and restored immune mediators, suggesting sustained inflammation reversal.
Area of Science:
- Immunology
- Hepatology
- Virology
Background:
- Hepatitis C Virus (HCV) infection leads to chronic inflammation.
- Direct-acting antiviral (DAA) therapy achieves sustained virological response (SVR) but long-term immune effects are unclear.
- Monocyte subsets and immune mediators may play a role in HCV pathogenesis and treatment response.
Purpose of the Study:
- To investigate the long-term impact of IFN-free sofosbuvir-based DAA treatment on peripheral monocyte subsets and immune mediators in Brazilian chronic HCV patients.
- To assess changes at sustained virological response (SVR) and one year after treatment completion (1y).
Main Methods:
- Flow cytometry was used to analyze monocyte subsets (CD14++CD16-, CD14++CD16+, CD14+CD16++).
- A multiplex assay measured 27 immune mediators.
- Samples were collected before treatment, at SVR, and 1 year post-treatment in monoinfected chronic HCV patients.
Main Results:
- While monocyte subset frequencies remained unchanged, monocyte activation markers (HLA-DR) decreased significantly at 1y compared to SVR.
- Twenty-one immune mediators showed significant downregulation at 1y, with 55-80% of patients exhibiting this reduction.
- Patients on DAA therapy demonstrated greater modulation of immune mediators at 1y.
Conclusions:
- Successful DAA therapy for HCV does not alter monocyte subset frequencies long-term.
- DAA treatment leads to reduced monocyte activation and sustained restoration of circulating immune mediators post-eradication.
- These findings suggest a potential for long-term reversal of inflammation following successful HCV treatment.
Introduction:
After DAA treatment for chronic hepatitis C infection, peripheral monocyte subsets from patients who achieved sustained virological response (SVR) reduced compared to healthy control. Improvement in inflammatory parameters and liver stiffness has been observed. However, little is known about the long-term impact of DAA treatment on peripheral monocyte subsets and immune mediators levels.
Objectives:
We aimed to examine peripheral monocyte subsets and immune mediators levels in Brazilian chronic HCV patients after long-term successful IFN-free SOF-based treatment.
Material And Methods:
We analyzed CD14++CD16-, CD14++CD16+ and CD14+CD16++ monocytes and 27 immune mediators by flow cytometry and analysis of multiple secreted proteins assay, respectively, in monoinfected chronic HCV patients receiving IFN-free sofosbuvir-based regimens followed before treatment, at SVR and one year after the end of treatment (1y).
Results:
Twenty-one biomarkers decreased significantly at 1y and 55-80 % of patients this reduction at 1y. Experimented patients presented a greater modulation of immune mediators at 1y. HLA-DR expression significantly decreased on CD14++CD16- and CD14++CD16+ monocytes at 1y when compared to SVR.
Conclusions:
Successful DAA therapy did not modify monocyte subsets frequency but reduced monocyte activation at 1y and sustained the downregulation and restoration of circulating immune mediators, indicating that long-term reversal of inflammation status could occur after HCV eradication.
More Related Videos
11:36Induction of Drug-Induced, Autoimmune Hepatitis in BALB/c Mice for the Study of Its Pathogenic Mechanisms
Published on: May 29, 2020
10:37Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix
Published on: October 20, 2021