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Detection of Low Copy Number Integrated Viral DNA Formed by In Vitro Hepatitis B Infection
Published on: November 7, 2018
Natural history of chronic hepatitis B virus infection: new light on an old story
1Hepatitis Research Center, National Taiwan University Hospital, Taipei.
Insights
Chronic hepatitis B virus (HBV) infection often becomes lifelong when contracted in infancy. The infection progresses through distinct phases, influencing host immune response and liver disease.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Chronic hepatitis B virus (HBV) infection is a major global health concern causing significant morbidity and mortality.
- Early infancy contraction leads to high rates of chronic infection, often persisting for life.
- Understanding the natural history and host-virus interactions is crucial for managing HBV.
Purpose of the Study:
- To elucidate the natural history of chronic HBV infection.
- To describe the distinct phases of HBV infection and their impact on host response.
- To analyze the complex virus-host interactions driving hepatic lesions.
Main Methods:
- Long-term follow-up studies of hepatitis B surface antigen (HBsAg) carriers.
- Clinicopathological analysis of liver tissues.
- Observation of viral replication dynamics and host immune tolerance.
Main Results:
- Chronic HBV infection evolves from a replicative phase to a non-replicative phase.
- Three distinct phases of virus-host interaction: tolerance, clearance, and residual integration.
- Immune tolerance occurs during active replication, with the liver often appearing normal.
Conclusions:
- Chronic HBV infection is characterized by dynamic phases of viral replication and host immune response.
- Virus-host interactions dictate the spectrum of liver disease in chronic HBV.
- Further research into these phases can inform therapeutic strategies.
Abstract:
Chronic hepatitis B virus (HBV) infection is one of the most common persistent virus infection in man. It causes significant morbidity and mortality, and therefore is important. Extensive studies on clinicopathologic studies and long-term follow up on hepatitis B surface antigen (HBsAg) carriers have largely disclosed the natural history of chronic HBV infection. The infection easily becomes chronic when contracted in early infancy. As high as 90% of babies born to HBV carrier mothers will also become HBsAg carriers. Once chronic infection is established, it is refractory, and HBsAg carriage usually persists for life. However, the chronic infection is not monotonous, it actually evolves from an HBV replicative phase to a non-replicative phase. The host responds differently and with more complexity in different phases. The virus-host interactions, divided into three phases, virus tolerance, virus clearance and residual HBV integrated phases, result in a heterogeneous variety of hepatic lesions. The first two phases occur when HBV is actively replicating, and the last corresponds to the non-replicative phase. The high HBV level (and hence HBV gene products) renders the host's immune system tolerant to the virus, and the infected host does not exert an effort to get rid of the virus. At this stage, the liver is nearly normal, and the host is asymptomatic. However, later in the replicative phase, the HBV replication begins to wane, and the immune tolerance is no longer maintained.(ABSTRACT TRUNCATED AT 250 WORDS)
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