Division of Infectious Diseases, Departments of Medicine & Medical Microbiology/Immunology, University of Alberta.
Provincial Laboratory for Public Health (Microbiology), University of Alberta Hospital, Edmonton.
J Pediatr Gastroenterol Nutr. 2019 May;68(5):e81-e84. doi: 10.1097/MPG.0000000000002318.
Hepatitis B virus (HBV) vaccination starting at birth is approximately 95% effective in preventing mother-to-child transmission to infants born to HBV-infected mothers. A higher risk of transmission is associated with birth to a highly viremic mother, often due to transplacental exposure, while later horizontal transmission is much less common, particularly following complete vaccination. This study reports a case of infection in an older child despite appropriate immunoprophylaxis starting at birth and an apparent protective immune response post-vaccination. Two immune escape mutations within the antigenic determinant of the surface antigen-coding region were observed in the child's dominant HBV sequence, whereas the maternal HBV variant lacked mutations at both sites. Ultra-deep sequencing confirmed the presence of 1 mutation at low levels within the maternal HBV quasispecies population, suggesting early exposure to the child followed by viral evolution resulting in immunoprophylaxis escape and chronic infection.
乙型肝炎病毒 (HBV) 疫苗接种从出生开始,对于预防 HBV 感染母亲所生婴儿的母婴传播,其有效率约为 95%。母婴传播的风险较高与高病毒血症母亲的分娩有关,通常是由于胎盘暴露所致,而后期的水平传播则较为少见,尤其是在完全接种疫苗后。本研究报告了一例在出生时即开始进行适当免疫预防接种的大龄儿童发生感染的病例,以及接种疫苗后出现的明显保护性免疫反应。在该儿童的 HBV 优势序列中,观察到表面抗原编码区抗原决定簇内的 2 个免疫逃逸突变,而母本 HBV 变异体在这两个位置均无突变。超深度测序证实,在母本 HBV 准种群体中低水平存在 1 个突变,提示该儿童在早期接触病毒后,病毒发生进化,导致免疫逃逸和慢性感染。