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Updated: Dec 27, 2025

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A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
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Current position of viral load versus hepatitis C core antigen testing
Antonio Aguilera1, Juan Carlos Alados2, Roberto Alonso3
1Servicio de Microbiología, Complejo Hospitalario Universitario de Santiago de Compostela y Departamento de Microbiología de la Universidad de Santiago de Compostela, Santiago de Compostela, A Coruña, España.
Summary
Hepatitis C virus (HCV) core antigen detection offers a cost-effective, rapid alternative to HCV RNA viral load testing for identifying active HCV infections, despite lower sensitivity in detecting low viremia.
Area of Science:
- Hepatology
- Virology
- Clinical Diagnostics
Background:
- Hepatitis C virus (HCV) RNA quantification (viral load) is standard for diagnosing active infection.
- HCV core antigen, a viral structural protein, also indicates replication.
- Core antigen testing offers advantages like lower cost, target stability, and faster results.
Purpose of the Study:
- To summarize current HCV viral load platforms, including point-of-care systems.
- To review indications for HCV core antigen testing in treatment guidelines.
- To discuss core antigen characteristics, available platforms, and its correlation with viral load.
Main Methods:
- Review of current HCV viral load determination platforms.
- Analysis of HCV core antigen characteristics and detection platforms.
- Correlation analysis between HCV core antigen and viral load measurements.
- Examination of clinical guidelines for HCV marker indications.
Main Results:
- HCV core antigen detection is a viable alternative to viral load testing for active infection diagnosis.
- Core antigen offers benefits in cost, stability, and speed, though with lower sensitivity at low viremia levels.
- Studies and guidelines support core antigen utility in identifying patients with active HCV infection.
Conclusions:
- HCV core antigen testing presents a valuable, practical tool for managing Hepatitis C.
- Its advantages make it suitable for various clinical settings, complementing viral load assays.
- Further evaluation of core antigen platforms and guideline integration is supported.

