Skip to content
- Hepatitis A
- Hepatitis B
- Hepatitis C
- Hepatitis D
- Hepatitis E
Hepatitis B Virus
- ds DNA virus
- Infective “Dane“ particle consists of inner core & outer coat
- Inner core contains DNA & DNA Polymerase
- Replicates within nuclei of infected hepatocytes
- surface coat added in the cytoplasm as the Hep B s Ag
Clinically
- Acute hepatitis
- Chronic hepatitis
- Cirrhosis
- HCC
Antibody-antigen complexes
- Hep B s Ag
- Australia antigen
- Associated with surface coat
- First evidence of infection & implies infectivity of blood
- Incubation period appears 1-6 weeks prior to biochemical or clinical illness
- Disappears during convalescence
- Anti HBs (antibody) appears weeks or months later
- It implies past infection & relative protection in future
- 10% will not have the antibody & they become chronic carriers
Hep B with Ag
- Core antigen
- Found in infected hepatocytes
- Not detectable in serum except using techiques that disrupt the Dane particle
- Antibody to it (Anti HBc) reflects active viral replication & appears early in illness
- Gradually reducing titre for years after
- Usually indicates past infection only
- Maybe only positive test in window period between HB s Ag disappearance & appearance of Anti HBs
Hep B e Ag
- Constituent of the core
- Found only in Hep B s Ag positive serum
- Indicates greater infectivity & greater chance of progression to chronic hepatitis
- Presence of antibody (Anti HBe) indicates less infectivity & more benign outcome
In Summary
- HBsAg
- Currently infected & Infectious
- Anti HBs
- Vaccinated or Post-Infection Immunity
- Anti HBc
- Post-Infection Immunity useful in window period between HBsAg disappearance & appearance of Anti HBs
- Others
- HBeAg
- Older marker of infectivity with greater chance of chronic hepatitis
- Anti-HBe
- Indicates less infectivity
- HBVDNA
- Direct marker infectivity
- Acute & Chronic Hepatitis
Epidemiology
- Parenteral spread
- High risk groups
- IV drug users
- Homosexuals
- Haemophiliacs
- Renal dialysis patients
- Extremely infectious groups
- IV drug abuse
- Homosexual
- Neonatal infection
- Transmission via sweat described through intact gloves from surgeon
- 1 million infective doses/ ml blood
- Most cases occur sporadically without known cause
- Vertical spread to infants common
- 5% of world population carriers
- Australia has a mosaic incidence due to multicultural population
- Kurri 10%
- Asia 10%
- South Europe 10%
- North Europe 0.1%
- Develop clinical hepatitis immunocompetent individuals 3/12 after exposure
- Immunocompromised patients tend to get Chronic Hepatitis
Hepatitis C (Non A-Non B)
- First recognised 1974
- ss RNA virus
- Usually presents in chronic form or as serological diagnosis
- Transmission
- Mainly IV Drug abuse
- Also in multiple transfusions (haemophilia)
- Little evidence for sex spread
- Commonest transmitted hepatitis via blood transfusions
- 0.5% blood donors positive
- Anti HCV within 3-6/12 of exposure
- Usually subclinical infection
- 20% patients no obvious source
- 40% proceed to chronic liver disease
- 20% carriers get cirrhosis at 20 years
- 5% get hepatocellular carcinoma
- Reduce by 25% the liver disease with Interferon usage
- Antibody production is the most useful marker for screening
- PCR testing is the best marker for infectivity
- Italian study showed 34.8% lifetime risk for a surgeon
Hepatitis D
- Defective RNA virus
- Can only replicate as co-infecting agent with Hep B
- Utilises the HB s Ag as surface shell
- Risk groups as Hep B
- Less common in health care workers & homosexuals
- Geographic variations
- 2-20% mortality
Hepatitis A & E
- Faecal contamination of water
- Developing countries only
Risk of Transmission
- Hepatitis B – 5-30% risk of transmission with needle stick
- Hepatitis C – 5%