SynthesisFrontiers in immunology2025
Cure of chronic hepatitis C virus infection after DAA treatment only partially restores the functional capacity of exhausted T cell subsets: a systematic review.
Synthesis in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
6 citing papers in PubMed.
- Mapping Determinants of Hepatitis C Virus E1/E2 Transmembrane Interactions Using Intergenotypic Chimeras.Viruses · 2026Article
- Hepatitis C Virus Infection Induces Autoimmune Hypothyroidism with Potential Profound Metabolic Implications: A Cross-Sectional Study in a High-Prevalence Region.Metabolites · 2026Article
- T cell dysfunction and metabolic disruption in chronic hepatitis C virus infection.Frontiers in immunology · 2026Review
- Liver reprogramming toward hepatocellular carcinoma following hepatitis C sustained virologic response: a narrative review.Translational gastroenterology and hepatology · 2026Review
- Immune correlates of outcomes after nucleos(t)ide analogue withdrawal in chronic hepatitis B: direct evidence, mechanistic context, and candidate biomarkers.Frontiers in immunology · 2026Review
- Evaluation of Hematological, Biochemical, and Coagulation Tests in Patients with Hepatitis C.Medicina (Kaunas, Lithuania) · 2025Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Chronic hepatitis C virus (HCV) infection drives T cells into a dysfunctional state due to persistent antigen exposure. This state persists despite viral clearance with previously used interferon-based treatments. Treatment exclusively with direct-acting antivirals (DAAs), introduced in 2014, has revolutionised HCV treatment with cure rates exceeding 95%. This systematic review investigates whether HCV cure by DAA treatment restores the functional capacity of different exhausted T cell subsets. Methods: We systematically searched the databases PubMed and Embase on June 26 Results: The search identified a total of 448 articles, with 35 articles eligible for full-text screening. Among these, 26 met the inclusion criteria and were included in this systematic review. A total of 919 individuals with chronic HCV infection were included. Following HCV cure, most T cell subsets showed only partial restoration of function. Notably, advanced stages of fibrosis were associated with sustained exhaustion across multiple T cell subsets. Conclusions: This systematic review found that exhausted T cell subsets are only partially restored after HCV cure by DAA treatment. Severe fibrosis, which can be considered a proxy for the duration of infection, appears to impede the reversal of the immune dysfunction. Further studies are warranted to better understand the influence of potential confounders such as age, sex, fibrosis stage, and duration of infection on the restoration of immune function to gain essential insights for future research. Systematic review registration: https://www.crd.york.ac.uk/prospero/, identifier CRD42024540474.
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