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Cell-mediated immunity to hepatitis B surface antigen in man.
Clinical and Experimental Immunology
|August 1, 1984
Summary
Delayed hypersensitivity skin tests and in vitro assays did not detect cell-mediated immunity to hepatitis B surface antigen (HBsAg) in individuals with natural hepatitis B virus (HBV) infection or after vaccination. These findings suggest cell-mediated immunity to HBsAg does not play a role in hepatitis B pathogenesis.
Area of Science:
- Immunology
- Hepatology
- Vaccinology
Background:
- Cell-mediated immunity is crucial for viral clearance and pathogenesis.
- The role of cell-mediated immunity to hepatitis B surface antigen (HBsAg) in hepatitis B virus (HBV) infection and vaccination is not fully understood.
Purpose of the Study:
- To investigate delayed hypersensitivity skin test reactivity and in vitro lymphocyte responses to HBsAg in individuals with varying HBV infection and vaccination statuses.
- To assess the role of cell-mediated immunity to HBsAg in the immunopathogenesis of acute and chronic type B hepatitis.
Main Methods:
- An aqueous hepatitis B virus (HBV) vaccine was used as an intradermal skin test antigen.
- Thirty-five individuals were tested: 10 seronegative, 10 HBsAg-positive (chronic carriers), and 15 anti-HBs-positive (5 vaccinated).
- Lymphocyte blastogenic responses to phytohaemagglutinin, concanavalin A, pokeweed mitogen, and purified HBsAg were assessed in vitro.
Main Results:
- Only one vaccinated individual with high anti-HBs titers showed a positive delayed skin test reaction to HBsAg.
- No subject exhibited a positive in vitro lymphocyte blastogenic response to HBsAg.
- Cell-mediated immune responses to HBsAg were not detected after natural HBV infection.
Conclusions:
- Delayed hypersensitivity skin test reactivity to HBsAg is rare, even in hyperimmunized individuals.
- In vitro assays failed to demonstrate cellular immunity to HBsAg, even in hyperimmunized persons.
- These studies provide no evidence that cell-mediated immunity to HBsAg is involved in the immunopathogenesis of acute or chronic type B hepatitis.