A pproximately 200 000 to 300 000 acute infections with hepatitis B virus (HBV) occur each year in the United States. More than 1 million persons have chronic HBV infection and ϳ5000 persons die each year from HBV-induced hepatocellular carcinoma and chronic liver disease in the United States.1,2 HBV is usually transmitted through sexual contact, exposure to blood or blood products, from mothers to neonates at birth, and inapparent percutaneous and permucosal exposures.Previous attempts at controlling HBV infection in the United States consisted of vaccinating high-risk populations and serologic screening of all pregnant women for hepatitis B surface antigen (HBsAg). However, these measures had little impact on the control of HBV infections; therefore, in 1992, the American Academy of Pediatrics recommended universal hepatitis B vaccination for newborns and routine vaccination of adolescents when feasible. Since then, immunization rates for newborns and adolescents with hepatitis B vaccine have steadily risen. The 2 currently available recombinant hepatitis B vaccines are Recombivax HB and Engerix B. Both contain purified recombinant HBsAg obtained by culturing genetically engineered Saccharomyces cerevisiae cells, which carry the surface antigen gene of HBV.
CASE REPORTAs part of a class function, a 17-year and 8-month-old male donated blood at a local blood collection center. One week later he received a letter indicating he tested positive for HBsAg and recommending review with his personal physician. He was also notified that his name was added to the confidential Deferred Donor Directory stating, "You are now permanently deferred from donating blood, plasma, tissues or organs for others." He was brought to the pediatric clinic for additional evaluation of HBV infection. On further review of the laboratory studies from the blood collection center, he was noted to have a reactive HBsAg by enzyme immunoassay (EIA), a positive HBsAg confirmatory test by neutralization, alanine aminotransferase (Ͻ100 IU/L), nonreactive antibody to hepatitis B core antigen, and nonreactive antibody to hepatitis C virus. Evaluation in the pediatric clinic revealed no risk factors for HBV infection. In further discussion with him, it was determined that he received his third Engerix B vaccination (20-g dose) 18 days before his blood donation. Physical examination did not reveal any abnormalities. Laboratory studies were obtained 48 days after his third hepatitis B vaccination and revealed a nonreactive HBsAg by EIA, asparate aminotransferase (25 IU/L; normal: 8 -42), alanine aminotransferase (14 IU/L; normal: 0 -55), total bilirubin (.4 mg/dL; normal: .2-1.2), and direct bilirubin (.2 mg/dL; normal: .0 -.4). Repeat laboratory studies were performed 117 days after his third hepatitis B vaccination and revealed a negative HBsAg by EIA, negative immunoglobulin G and immunoglobulin M antibodies to hepatitis B core antigen by EIA, and a positive antibody to HBsAg. This is consistent with successful hepatitis B immunization.HBsAg is the ...