Hepatitis B virus (HBV) infection is a global health issue. Universal infantile hepatitis B (HB) vaccination is very efficacious. However, HBV infections among those immunized subjects have been reported. The long-term efficacy of postnatal passive-active HB vaccination in high-risk subjects is not well explored. A total of 8,733 senior high school students who were born after July 1987 were assayed for hepatitis B surface antigen (HBsAg) and antibodies to HBsAg (anti-HBs). The overall HBsAg and anti-HBs-positive rates were 1.9% and 48.3%, respectively. The HBsAg-positive rate was 15% in HB immunoglobulin (HBIG) recipients (adjusted odds ratio [OR]: 15.63; 95% confidence interval [CI]: 10.99-22.22). Among students who did not receive HBIG, there was a significantly negative association between HB vaccination dosage and HBsAg-positive rate (P for trend 5 0.011). Adjusted ORs for those who received 4, 3, and 1 to 2 doses were 1.00, 1.52 (95% CI: 0.91-2.53), and 2.85 (95% CI: 1.39-5.81), respectively. Among HBIG recipients, the HBsAgpositive rate was significantly higher in subjects with maternal hepatitis B e antigen (HBeAg) positivity and who received HBIG off-schedule. A booster dose of HB vaccination was administered to 1974 HBsAg-and anti-HBs-negative subjects. Prebooster and a postbooster blood samples were drawn for anti-HBs quantification. The proportions of postbooster anti-HBs titer <10 mIU/mL was 27.9%. Subjects with prebooster anti-HBs titers of 1.0-9.9 mIU/mL had significantly higher postbooster anti-HBs titers than those with prebooster anti-HBs titers of <1.0 mIU/mL (P < 0.0001). Conclusion: Having maternal HBeAg positivity is the most important determinant for HBsAg positivity in adolescents who received postnatal passive-active HB vaccination 15 years before. A significant proportion of complete vaccinees may have lost their immunological memories against HBsAg. (HEPATOLOGY 2013;57:38-45) H epatitis B virus (HBV) infection is a global issue, affecting two billion people in the world, with 360 million chronic carriers of hepatitis B surface antigen (HBsAg).1 The sequalae of chronic HBV infection, including hepatic failure, liver cirrhosis, and hepatocellular carcinoma, shorten lives and impose great economic burdens on society.Taiwan has been an endemic area of HBV infection, with an HBV infection rate of 95% and a 15%-20% HBsAg carrier rate in the general population.2 Vertical transmission is the main cause of persistent HBV infection in Taiwan 3 ; fortunately, it can be blocked by passive-active vaccination after birth. [4][5][6] To control HBV infection, a hepatitis B (HB) vaccination program was launched in Taiwan in 1984, starting with newborns of highly infectious mothers, and expanded to all newborns in 1986.
7The remarkable effectiveness of universal infantile HB vaccination program (UIHBVP) is well documented. [8][9][10][11][12] In Taiwan, the HBV infection and carrier rates of children born after the program has declined dramatically. [10][11][12] The incidence of infantile fulminant he...