[Getting to zero mother-to-child transmission of hepatitis B virus: dream and challenge]

Zhonghua Gan Zang Bing Za Zhi. 2018 Apr 20;26(4):262-265. doi: 10.3760/cma.j.issn.1007-3418.2018.04.006.
[Article in Chinese]

Abstract

To eliminate viral hepatitis as a public health threat, the World Health Organization has set the ambitious goal of reducing the prevalence of hepatitis B surface antigen (HBsAg) in children to 0.1% by 2030, and the key to this grand goal is cutting off hepatitis B virus (HBV) transmission from mother-to-child. Previously, national and international guidelines for the management of chronic hepatitis B recommended the use of hepatitis B vaccine and hepatitis B immunoglobulin (HBIG) or combination of any in neonates and antiviral drugs for pregnant women with high viral load in late pregnancy. However, a recent study in Thailand found that the addition of antiviral drugs in pregnant women with high viral load in the third trimester did not significantly lower the incidence of mother-to-child HBV transmission, but no case of chronic HBV infection was seen with strict standards hepatitis B vaccine and HBIG combined immunoprophylaxis and the use of tenofovir disoproxil in pregnant women with high viral load in the third trimester. In addition, the incidence of mother -to- child transmission of HBV in the antiviral group was 0, while the incidence of HBV transmission in the placebo group was 2%. Therefore, it is not possible to deny the efficacy of adding antiviral drugs in treating pregnant women with high viral load in the third trimester with combined immunoprophylaxis. There is an urgent need for more real-world studies in clinical practice to further reveal the principles and existing problems of mother- to- child transmission of HBV.

为消除病毒性肝炎对公共卫生的威胁,世界卫生组织提出到2030年要实现儿童乙型肝炎表面抗原流行率降至0.1%的宏伟目标,而乙型肝炎病毒(HBV)母婴阻断是实现这一宏伟目标的关键。近年来,国内外主要慢性乙型肝炎管理指南推荐,在新生儿注射乙型肝炎疫苗和乙型肝炎免疫球蛋白(HBIG)联合免疫基础上,对妊娠晚期高病毒载量孕妇加用抗病毒药物,可以进一步减少甚至完全阻断HBV母婴传播。然而,近期在泰国的一项研究发现,对高病毒载量孕妇在妊娠晚期加用抗病毒药物并没有显著降低HBV母婴传播的发生率,但是该研究发现,通过严格标准的乙型肝炎疫苗和HBIG联合免疫,以及对妊娠晚期高病毒载量孕妇使用替诺福韦酯,无一例婴儿发生慢性HBV感染,即加用抗病毒药物组HBV母婴传播发生率为0,而安慰剂组HBV母婴传播发生率为2.0%。因此,尚不能否定在联合免疫的基础上,对高病毒载量孕妇在妊娠晚期加用抗病毒药物的有效性。临床实践中迫切需要更多真实世界研究,进一步揭示HBV母婴传播的规律及存在的问题。.

Keywords: Hepatitis B immunoglobulin; Hepatitis B vaccines; Hepatitis B virus; Mother-to-child transmission.

MeSH terms

  • Antiviral Agents / therapeutic use
  • Child
  • Female
  • Hepatitis B / drug therapy
  • Hepatitis B / prevention & control*
  • Hepatitis B Surface Antigens / blood
  • Hepatitis B Vaccines / administration & dosage
  • Hepatitis B Vaccines / therapeutic use*
  • Hepatitis B e Antigens / blood
  • Hepatitis B virus / immunology*
  • Humans
  • Immunoglobulins / administration & dosage
  • Immunoglobulins / therapeutic use*
  • Infant, Newborn
  • Infectious Disease Transmission, Vertical / prevention & control*
  • Pregnancy
  • Pregnancy Complications, Infectious / diagnosis
  • Pregnancy Complications, Infectious / drug therapy*
  • Pregnancy Complications, Infectious / virology
  • Pregnancy Trimester, Third
  • Viral Load

Substances

  • Antiviral Agents
  • Hepatitis B Surface Antigens
  • Hepatitis B Vaccines
  • Hepatitis B e Antigens
  • Immunoglobulins
  • hepatitis B hyperimmune globulin