[The vaccinal prevention of the HBsAg carrier state among newborn infants]
Insights
Hepatitis B (HB) vaccination is crucial for newborns. Early vaccination prevents chronic Hepatitis B surface antigen (HBsAg) carrier states, with vaccinated infants showing significantly lower antigen and higher antibody rates.
Area of Science:
- Hepatology
- Immunology
- Pediatrics
Background:
- Hepatitis B virus (HBV) infection poses a significant risk to newborns born to mothers with antigenemia.
- The development of a chronic Hepatitis B surface antigen (HBsAg) carrier state in infants is influenced by the timing of initial detection.
- A stable HBsAg carrier state in infants typically forms after the first three months of life.
Purpose of the Study:
- To investigate the time course of the HBsAg carrier state in infants born to HBsAg-positive mothers.
- To evaluate the efficacy of a national plasma-derived hepatitis B vaccine in preventing HBsAg carrier state in newborns.
- To analyze epidemiological factors contributing to HBV infection in infants.
Main Methods:
- Longitudinal monitoring of HBsAg carrier status in infants.
- Epidemiological survey of 185 infants who developed hepatitis B.
- Assessment of vaccine efficacy through observation of vaccinated newborns and a control group.
Main Results:
- Vaccinated infants (3 doses at 0, 1, 6 months) showed a 3.3% HBsAg detection rate and 80% antibody detection rate.
- Control group infants exhibited a significantly higher HBsAg detection rate (23.7%) and lower antibody detection rate (8.0%).
- The study highlights the dependence of the infant carrier state pattern on the timing of initial antigen detection.
Conclusions:
- Hepatitis B vaccination is essential for preventing the chronic HBsAg carrier state in newborns.
- The national plasma vaccine demonstrates high efficacy in protecting infants against HBV infection and carrier status.
- Early intervention and vaccination strategies are critical for managing perinatal HBV transmission.
Abstract:
The paper presents the data on the time course of HBsAg carrier state in babies born to mothers with antigenemia indicating the dependence of the pattern of the antigen carrier state in babies upon the time of its primary detection. The stable (chronic) HBsAg carrier state in babies was shown to be formed after the first 3 months of life which attests to the necessity of using a vaccine against hepatitis B (HB) for prevention of HBsAg carrier state in newborns. The results of epidemiological survey in 185 babies developing HB with the analysis of all possible factors of their infection contraction are presented. The efficacy of the national plasma vaccine against hepatitis B is evaluated in observations of the newborn babies whose mothers were carriers of HBsAg. It was established that in vaccinated babies after 3 injections of the vaccine at 0, 1, and 6 months the rate of antigen detection was 3.3% and that of antibody 80% whereas in babies of the control group these values were 23.7% and 8.0%, respectively.
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