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Redefining MTCT prevention strategies toward HBV elimination: Editorial on “Factors associated with hepatitis B mother-to-child transmission in a national prevention program”

Clinical and Molecular Hepatology 2026;32(2):943-945.
Published online: July 14, 2025

Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea

Corresponding author : Young-Sun Lee Department of Internal Medicine, Division of Gastroenterology and Hepatology, Guro Hospital, Korea University College of Medicine, 148 Gurodong-ro, Guro-gu, Seoul 08308, Korea Tel: +82-2-2626-1030, Fax: +82-2-2626-1038, E-mail: lys810@korea.ac.kr

Editor: Han Ah Lee, Chung-Ang University College of Medicine, Korea

• Received: July 8, 2025   • Accepted: July 11, 2025

Copyright © 2026 by The Korean Association for the Study of the Liver

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Chronic hepatitis B virus (HBV) infection remains a major global health challenge, with 1.23 million new infections worldwide in 2022 [1]. Mother-to-child transmission (MTCT) contributes substantially to chronic HBV infections; thus, primary prevention is important for achieving HBV elimination [1]. In addition to active-passive HBV immunization of newborns, administration of tenofovir disoproxil fumarate to pregnant mothers with HBV DNA titer (≥200,000 IU/mL) effectively prevented MTCT [2]. However, evidence supporting other preventive strategies, such as breastfeeding and cesarean section for preventing MTCT, remains insufficient.
A study by Ki et al. provided valuable large-scale, real-world longitudinal data regarding factors associated with MTCT [3]. This population-based cohort study included HBV status data from 154,478 mothers-infant pairs from the Perinatal Hepatitis B Prevention Program (PHBPP) of South Korea from 2002–2021. Reimbursement records from the Korean National Health Insurance were merged with the PHBPP data to include antiviral prescriptions and delivery methods in the analysis. Maternal antiviral use, hepatitis B e antigen (HBeAg)-negative status, cesarean section, and breastfeeding were associated with lower MTCT rates.
The World Health Organization (WHO) and European Association for the Study of the Liver (EASL) recommend tenofovir prophylaxis for pregnant women with a high viral load [4,5]. This study by Ki et al. also showed a significantly lower MTCT rate with antiviral therapy (0.9% vs. 2.4%). Mothers with HBeAg, which was correlated with a high viral load, were found to be the most effective (1.0% vs. 5.9%). Unfortunately, the maternal HBV DNA titer was unavailable, and risk stratification based on the titer level was impossible. The MTCT rates were similar between the initiation of antiviral therapy at weeks 14–27 (0.39%) and 28–32 (0.44%). This is comparable to a recent randomized trial in which maternal tenofovir prophylaxis from week 16 with infant HBV immunization was non-inferior to the initiation of at tenofovir week 28 with the administration of HBV immunoglobulin and vaccination after birth [6].
This study addressed whether cesarean section can reduce the risk of MTCT. The authors reported that cesarean section showed a lower MTCT risk than vaginal delivery, even after adjusting for other variables (1.9% vs. 2.6%). However, this should be interpreted with caution because cesarean sections carry the risk of short- and long-term complications for the mother [7]. He et al. suggested that cesarean section may be beneficial in reducing MTCT (pooled odds ratio 0.42, 95% confidence interval 0.23–0.76) [8]; however, another single center prospective cohort study showed no statistical difference in MTCT rate between delivery methods [9]. Cesarean section has been reported to reduce MTCT in mothers with HBV DNA levels ≥200,000 IU/mL [10], but since antiviral therapy effectively lowers maternal viral load, it may be sufficient to prevent MTCT without the need for cesarean delivery. The EASL recommended that cesarean section may be beneficial for high HBV titers and HBeAg-positive Asian mothers in 2023 [11], but no recommendations were provided about cesarean section in their most recent guidelines [5].
Concerns about the transmission of HBV through breast milk often hinder breastfeeding postpartum. However, breastfeeding was shown to be safe if active-passive immunization performed for infants [12]. Moreover, this study shows breastfeeding may be beneficial in reducing MTCT compared to formula feeding (1.8% vs. 2.8%). Pan et al. found that breastfeeding modestly reduces MTCT (relative risk 0.74; 95% confidence interval 0.56–0.98) [9], supporting the protective effect of breastfeeding. Luo et al. showed that lactoferrin in breast milk binds to hepatitis B surface antigen and inhibits HBV [13]. Breastfeeding is known to protect infants against human immunodeficiency virus vertical transmission through multiple factors, such as healthy microbiome, lactoferrin, elafin, and other innate immune factors, which may apply to HBV [14]. However, precautionary measures should be considered if mothers have cracked nipples or infants with oral ulcers.
Fortunately, the rate of MTCT has decreased over time from 3.6% (2002–2005) to 1.3% (2018–2021). The authors stated that older maternal age and the use of antiviral prophylaxis may have contributed to this trend. The rate of cesarean section is steadily increasing in South Korea, from 36.9% in 2012 to 58.7% in 2021 [15]. Improvement in socioeconomic status, multiple gestations induced by fertility treatments, and obesity may have contributed to an increase in cesarean sections. As cultural backgrounds and societies differ globally, the generalizability of the findings may be limited. Nonetheless, this research supports progress toward the WHO’s goal of eliminating HBV.

Authors’ contribution

Conception or design of the work: E. Choi and Y-S. Lee; Drafting the article: E. Choi and Y-S. Lee; Critical revision of the article: E. Choi and J.H. Lee; Final approval of the version to be published: Y-S. Lee.

Acknowledgements

This study was supported by a National Research Foundation of Korea grant from the Korean government (the Ministry of Education, Science and Technology, RS-2021-NR061523), a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), South Korea funded by the Ministry of Health & Welfare, Republic of Korea (RS-2024-00439963), and Korea University Guro Hospital (KOREA RESEARCHDRIVEN HOSPITAL) and Korea University (K2512711).

Conflicts of Interest

The authors have no conflicts of interest to declare.

EASL

European Association for the Study of the Liver

HBeAg

hepatitis B envelope antigen

HBV

hepatitis B virus

MTCT

mother-to-child transmission

PHBPP

Perinatal Hepatitis B Prevention Program

WHO

World Health Organization
  • 1. World Health Organization. Global hepatitis report 2024: action for access in low-and middle-income countries. Geneva: World Health Organization; 2024.
  • 2. Lee YS, Lee HS, Kim JH, Chang SW, Hyun MH, Bak H, et al. Role of tenofovir disoproxil fumarate in prevention of perinatal transmission of hepatitis B virus from mother to child: a systematic review and meta-analysis. Korean J Intern Med 2021;36:76-85.
  • 3. Ki M, Kim BW, Baik D, Kim JH. Factors associated with hepatitis B mother-to-child transmission in a national prevention program. Clin Mol Hepatol 2025 Jun 24. doi: 10.3350/cmh.2025.0214.
  • 4. World Health Organization. Prevention of mother-to-child transmission of hepatitis B virus: Guidelines on antiviral prophylaxis in pregnancy. Geneva: World Health Organization; 2020.
  • 5. European Association for the Study of the Liver. EASL Clinical Practice Guidelines on the management of hepatitis B virus infection. J Hepatol 2025;83:502-583.
  • 6. Pan CQ, Dai E, Mo Z, Zhang H, Zheng TQ, Wang Y, et al. Tenofovir and hepatitis B virus transmission during pregnancy: A randomized clinical trial. JAMA 2025;333:390-399.
  • 7. Larsson C, Djuvfelt E, Lindam A, Tunón K, Nordin P. Surgical complications after caesarean section: A population-based cohort study. PLoS One 2021;16:e0258222.
  • 8. He R, Wen P, Xiong M, Fan Z, Li F, Luo D, et al. Cesarean section in reducing mother-to-child HBV transmission: a meta-analysis. J Matern Fetal Neonatal Med 2022;35:3424-3432.
  • 9. Pan YC, Jia ZF, Wang YQ, Yang N, Liu JX, Zhai XJ, et al. The role of caesarean section and nonbreastfeeding in preventing mother-to-child transmission of hepatitis B virus in HBsAg-and HBeAg-positive mothers: results from a prospective cohort study and a meta-analysis. J Viral Hepat 2020;27:1032-1043.
  • 10. Pan CQ, Zou HB, Chen Y, Zhang X, Zhang H, Li J, et al. Cesarean section reduces perinatal transmission of hepatitis B virus infection from hepatitis B surface antigen-positive women to their infants. Clin Gastroenterol Hepatol 2013;11:1349-1355.
  • 11. European Association for the Study of the Liver. EASL Clinical Practice Guidelines on the management of liver diseases in pregnancy. J Hepatol 2023;79:768-828.
  • 12. Zhou M, Li L, Han L, Sun F, Yi N. Breast-feeding is not a risk factor of mother-to-child transmission of hepatitis B virus. Int J Gen Med 2021;14:1819-1827.
  • 13. Luo Y, Xiang K, Liu J, Song J, Feng J, Chen J, et al. Inhibition of in vitro infection of hepatitis B virus by human breastmilk. Nutrients 2022;14:1561.
  • 14. Henrick BM, Yao XD, Nasser L, Roozrogousheh A, Rosenthal KL. Breastfeeding behaviors and the innate immune system of human milk: Working together to protect infants against inflammation, HIV-1, and other infections. Front Immunol 2017;8:1631.
  • 15. Kim S, Oh JW, Yun JW. Narrative review on the trend of childbirth in South Korea and feasible intervention to reduce cesarean section rate. J Korean Soc Matern Child Health 2023;27:1-13.

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Redefining MTCT prevention strategies toward HBV elimination: Editorial on “Factors associated with hepatitis B mother-to-child transmission in a national prevention program”
Clin Mol Hepatol. 2026;32(2):943-945.   Published online July 14, 2025
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Redefining MTCT prevention strategies toward HBV elimination: Editorial on “Factors associated with hepatitis B mother-to-child transmission in a national prevention program”
Clin Mol Hepatol. 2026;32(2):943-945.   Published online July 14, 2025
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Redefining MTCT prevention strategies toward HBV elimination: Editorial on “Factors associated with hepatitis B mother-to-child transmission in a national prevention program”
Redefining MTCT prevention strategies toward HBV elimination: Editorial on “Factors associated with hepatitis B mother-to-child transmission in a national prevention program”