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Short Communication: Hepatology

Horizontal Transmission of Hepatitis B Virus From Mother to Child Due to Immune Escape Despite Immunoprophylaxis

Kanji, Jamil N.∗,†; Penner, Robert E.D.; Giles, Elizabeth; Goodison, Karin§; Martin, Steven R.; Marinier, Eric; Osiowy, Carla

Author Information
Journal of Pediatric Gastroenterology and Nutrition: May 2019 - Volume 68 - Issue 5 - p e81-e84
doi: 10.1097/MPG.0000000000002318


What Is Known

  • Although uncommon, breakthrough infection with hepatitis B virus can occur in infants born to chronically infected mothers despite complete immunoprophylaxis at birth.
  • A higher risk of breakthrough infection is associated with maternal hepatitis B e-antigen positivity, high maternal hepatitis B virus DNA levels (>7 log10 IU/mL) and potentially, surface antigen immune escape mutations such as G145R.

What Is New

  • A rare delayed onset of breakthrough infection in a child due to an immune escape mutant transmitted from the mother occurred despite an apparent vaccine response.

Due to the extremely high risk of developing chronic hepatitis B virus (HBV) infection in young infants exposed to the virus, vaccination, and delivery of hepatitis B immunoglobulin (HBIg) within 12 hours of birth are crucial and effective (85%–95%) measures to prevent infection in infants born to mothers chronically infected with HBV. Reports of vaccine breakthrough, or more accurately, “failure to clear infection” (1), in infants or children is infrequent following complete immunoprophylaxis, but has been associated with intrauterine or perinatal exposure to the virus (2) or in rare cases, evolution and expansion of isolates having mutations within the viral genome resulting in escape from neutralization by antibodies elicited to the vaccine or present in immunoglobulin (ie, immune escape; (3)). These immune escape mutations are often transmitted from the mother or they may emerge as de novo mutations (1), although studies have shown that infants born to mothers having HBV immune escape mutations successfully respond to vaccination and are protected against infection (4). A glycine to arginine substitution at amino acid 145 (G145R) within the antigenic determinant of the hepatitis B surface antigen (HBsAg) protein (aa 124–147) is the most common mutation described to result in immune escape following vaccination (5,6). Although still rare, immune escape due to G145R is more commonly associated with HBV reactivation following transplantation or immunosuppressive treatments (7,8). The present study describes a breakthrough HBV infection in a child having HBsAg mutations at amino acids 144 and 145 despite appropriate and complete immunoprophylaxis starting at birth and an apparent vaccine-induced response following completion of vaccination.


Case Patient

A 5-year-old girl was referred for evaluation of chronic HBV infection. She was the product of a normal pregnancy, born in 2012 via spontaneous vaginal delivery at term with no complications. Her mother was diagnosed with HBV 4 months before delivery based upon a confirmed HBsAg and positive total HBV core antibody (anti-HBc) result, but otherwise had an uncomplicated pregnancy with no gestational diabetes, hypertension, other infections, or delivery complications. The mother's HBV viral load was unknown before and at the time of delivery, and she had no history of antiviral treatment. The patient received HBIg (0.5 mL intramuscular) and HBV vaccine at birth with subsequent HBV vaccine doses at 2 and 6 months of age. Serum samples for this study were collected from the child at 4 years 10 months of age and from the mother at approximately 3.5 and 4.5 years after the birth of the child (samples M1 and M2, respectively).

HBV DNA Sequencing

Sera (150 μL) were extracted for HBV DNA, amplified and sequenced using primers targeting the HBsAg-coding region as described previously (9). Massively parallel deep amplicon-based sequencing of the HBsAg, Polymerase, and Core coding regions was performed using methods and primer sequences provided in the Supplemental Digital Content (Text, Supplemental Digital Content 1, and Tables 1 and 2, Supplemental Digital Content 2, Deep sequencing analysis was performed on the mother–child paired samples to evaluate the quasispecies complexity within each sample and to determine the presence of low-level mutant or wild-type populations within the mother or child, respectively. Quasispecies complexity measures were performed as described in the Supplemental Digital Content (Text, Supplemental Digital Content 1,


The hepatitis B surface antibody (anti-HBs) titer of the patient was tested approximately 1 month following the third dose of vaccine at 7 months 19 days of age and was found to be 588.8 IU/L with no evidence of circulating HBsAg (anti-HBs value >10–12 IU/L is considered to be protective/immune). At 4 years 10 months of age, the patient was re-tested for hepatitis B serologic markers due to parental anxiety and found to be neutralization-confirmed HBsAg positive. On the same serum draw, she was seropositive for total anti-HBc, HBV e-antigen (HBeAg), and negative for anti-HBc IgM and anti-HBeAg antibody. Her anti-HBs titre was 9.68 IU/L with a detectable HBV viremia quantified at 127,993 IU/mL (5.1 log10). Alanine aminotransferase level was within normal range at 26 U/L (normal <33). Repeat serologic testing 3 and 15 months later confirmed these results and established the development of chronic hepatitis B infection.

The patient was up-to-date with her vaccinations and had not received any further HBV vaccine doses. Other than her mother, all other house-hold members were found negative for HBV around the time of her diagnosis. Both the patient and her mother are HBeAg positive and thus deemed to be in the immune tolerant phase of HBV infection with unremarkable abdominal ultrasound findings. The patient's viral load has ranged from 5.1 to 5.3 log10 IU/mL since diagnosis in 2017 and her mother's has ranged from 8.2 to 8.7 log10 IU/mL since 2014, with neither treated with antiviral medication nor any abnormality in serum bilirubin, aminotransferases, or alpha-fetoproteins observed.

Based on the acquisition of HBV infection despite an apparent robust immune response at the age of 7 months 19 days and a complete course of immunoprophylaxis starting at birth, sequencing of HBV isolates from both the patient and her mother was undertaken. Both isolates typed as genotype B by direct sequencing and both had identical sequences throughout the partial HBsAg region (364 nucleotides), apart from 2 mutations in the child's sequence resulting in D144E/G145R amino acid substitutions within the HBsAg antigenic determinant. Deep sequence analysis showed that both maternal samples contained extremely low quasispecies population levels having substitutions at either D144 or G145, yet mutations at both sites were not observed in combination on any of the mother's sequence reads (Table 1). Only the more recent maternal sample M2 (4.5 years after birth of child) had a G145R quasispecies population above the experimental error rate. The child's sample also had an extremely low wild type G145 population, but wild type D144 sequence populations were not observed above the experimental error rate.

Frequency of wild-type or mutant amino acid residue at site 144 and 145 of the hepatitis B surface antigen antigenic determinant following deep sequencing

The number of dominant quasispecies populations among the child's sample was greatly reduced compared to the mother's samples (Table 2). Similarly, complexity measures of incidence (number of haplotypes, polymorphic sites, and unique mutations) and abundance (maximum mutation frequency (Mfm), population nucleotide diversity (π), and Simpson index (HSi)) showed that overall, the child's isolate had reduced genetic diversity compared to the maternal isolate at different time periods (Table 3). Although the Mfm and π were reduced among immune targets such as the core and surface antigen regions of the virus, the polymerase-coding region investigated (nt 803–1153) from the child displayed a similar or even higher mutation and population nucleotide diversity as the mother's isolates, suggesting the influence of multiple, and varied evolutionary influences following transmission and infection.

Number of quasispecies populations per patient sample showing the percentage of total hepatitis B surface antigen region deep-sequencing reads per population
Measures of quasispecies complexity and genetic diversity by genomic region (core, polymerase, surface antigen)


HBV vaccination starting at birth is approximately 95% effective (10). Aside from host factors that may interfere with vaccine response (host genetics, immune status, etc), virological factors, such as maternal HBV DNA levels (>7 log10 IU/mL; (11)) and HBeAg positivity, can have a significant impact on the risk of chronic infection in infants born to chronically infected mothers. Although reports have suggested the prevalence of HBsAg mutants are increasing, which may compromise the long-term success of vaccination programs (12), it has been repeatedly shown that mutations verified to result in immune escape, such as G145R, remain a rare exceptional cause of vaccine breakthrough, and that over time the HBsAg mutation frequency has not accelerated due to immunization (13). Indeed, the recombinant vaccine was shown to durably protect against challenge with a G145R variant in a vaccinated chimpanzee model (14).

In the present study, an unusual occurrence of late (>7 months of age) infection breakthrough despite complete HBV immunoprophylaxis starting at birth was observed. The breakthrough was likely associated with the presence of immune escape mutations (D144E/G145R) dominant within the child's isolate and the higher risk posed by the mother's HBeAg positivity and presumed high HBV viral load at the time of birth. To reduce the risk of mother to child transmission, patient management guidelines recommend antiviral therapy for women with a viral load >5.3 to 7.3 log10 IU/mL in the third trimester of pregnancy (2,15). The mother's viral load at the time of birth is unknown; however, due to her immunotolerant phase and consistently high HBV DNA levels post-pregnancy it is assumed that she also had a high HBV viral load at birth. Amino acids 144 and 145 fall within a conformational epitope in the second loop of the HBsAg antigenic determinant. These amino acids are crucial for immunogenicity via the proper display and structure of the epitope (5,16), with mutations resulting in reduced antibody binding affinity and virion stability (16).

Due to the rapid rate of HBV replication and mutation under the control of an error-prone polymerase (17), a viral quasispecies population results, composed of a multitude of closely related but non-identical viral genomes due to random point mutations. A quasispecies nature allows flexibility among the viral population during periods of selective pressures resulting in selection of adaptive or most fit strains. Immuno-prophylaxis and the vaccine immune response are selective pressures which likely drive nucleotide substitution (18). In this study, an extremely low population level (<2%) of R145 or G145 sequences was observed within the total HBV quasispecies of the mother or child, respectively, as was the lack of a detectable E144 mutant population in the mother. This suggests that quasispecies populations containing R145 were selected in the child following transmission which continued to evolve and expand under immunoprophylaxis-based immune pressure to establish the dominant haplotype iteration observed at the time of sampling. As a specific founder haplotype was not observed among the mother's HBV quasispecies, it possibly indicates that the child's dominant populations were either not transmitted or they became extinct within the mother's HBV quasispecies over the intervening time. The observation of overall reduced genetic diversity among the child's quasispecies compared to the maternal isolate at different time periods is consistent with the evolutionary bottleneck that occurs with HBV transmission (19). Pressure from immunoprophylactic extrinsic and intrinsic forces acts upon the transmitted HBV population to select specific quasispecies genomic variants, such as those able to evade neutralizing or B-cell responses, thus narrowing the number of haplotypes (1). The mutation frequency and level of complexity among genomic regions of the haplotypes differed, such that the polymerase region of the child's isolate was similar or slightly higher than that observed with the mother's isolates. This is likely the result of different evolutionary pressures acting upon the viral genome, such as immune-based pressures or the evolutionary constraints of overlapping open reading frames.

Immune escape mutations have been more frequently observed in vaccinated infants having a late onset of infection (≥6 months after birth), suggesting that the infants were likely non-responders to the vaccine (6). Although post-vaccination testing of the child in this study indicated an apparent vaccine-induced immune response (588.8 IU/L), there is the possibility that testing before 9 months of age missed a prolonged HBV incubation, or measurement of the actual vaccine-mediated antibody response was confounded by detection of passive anti-HBs from HBIg administered at birth, the latter being rather unlikely. Post-vaccination testing of infants born to infected mothers and vaccinated at birth is recommended at least 1 month following the last dose of vaccine and/or at least 9 months after birth (20). Despite the reduced genomic complexity observed with the child's HBV isolate, the precise time of transmission cannot be determined and may have occurred at any point >7 months of age. The current study underlines the risk, however small, of the failure by some infants to adequately clear infection following birth to a highly viremic mother, despite appropriate immunoprophylaxis and response, due in part to HBV immune escape mutations.


1. May S, Mandal S, Keel P, et al. Hepatitis B virus immunization and neonatal acquisition of persistent infection in England and Wales. J Infect Dis 2018; 218:726–733.
2. Visvanathan K, Dusheiko G, Giles M, et al. Managing HBV in pregnancy. Prevention, prophylaxis, treatment and follow-up: position paper produced by Australian, UK and New Zealand key opinion leaders. Gut 2016; 65:340–350.
3. Coppola N, Onorato L, Minichini C, et al. Clinical significance of hepatitis B surface antigen mutants. World J Hepatol 2015; 7:2729–2739.
4. Komatsu H, Inui A, Umetsu S, et al. Evaluation of the G145R mutant of the hepatitis B virus as a minor strain in mother-to-child transmission. PLoS One 2016; 11:e0165674.
5. Carman WF, Zanetti AR, Karayiannis P, et al. Vaccine-induced escape mutant of hepatitis B virus. Lancet 1990; 336:325–329.
6. Stevens CE, Toy P, Kamili S, et al. Eradicating hepatitis B virus: the critical role of preventing perinatal transmission. Biologicals 2017; 50:3–19.
7. Locarnini S, Shouval D. Commonly found variations/mutations in the HBsAg of hepatitis B virus in the context of effective immunization programs: questionable clinical and public health significance. J Virol 2014; 88:6532.
8. Inoue J, Kondo Y, Wakui Y, et al. Reactivation of resolved hepatitis B virus infection with immune escape mutations after long-term corticosteroid therapy. Clin J Gastroenterol 2016; 9:93–98.
9. Lau KCK, Osiowy C, Giles E, et al. Deep sequencing shows low-level oncogenic hepatitis B virus variants persists post-liver transplant despite potent anti-HBV prophylaxis. J Viral Hepat 2018; 25:724–732.
10. Osiowy C. From infancy and beyond... ensuring a lifetime of hepatitis B (HBV) vaccine-induced immunity. Hum Vaccine Immunother 2018; 14:2093–2097.
11. Chen HL, Zha ML, Cai JY, et al. Maternal viral load and hepatitis B virus mother-to-child transmission risk: a systematic review and meta-analysis. Hepatol Res 2018; 48:788–801.
12. Lai MW, Lin TY, Tsao KC, et al. Increased seroprevalence of HBV DNA with mutations in the s gene among individuals greater than 18 years old after complete vaccination. Gastroenterology 2012; 143:400–407.
13. Yan B, Lv J, Feng Y, et al. Temporal trend of hepatitis B surface mutations in the post-immunization period: 9 years of surveillance (2005–2013) in eastern China. Sci Rep 2017; 7:6669.
14. Ogata N, Cote PJ, Zanetti AR, et al. Licenced recombinant hepatitis B vaccines protect chimpanzees against infection with the prototype surface gene mutant of hepatitis B virus. Hepatology 1999; 30:779–786.
15. Terrault N, Feld JJ, Lok AS. Tenofovir to prevent perinatal transmission of hepatitis B. N Engl J Med 2018; 378:2348–2349.
16. Rezaee R, Poorebrahim M, Najafi S, et al. Impacts of the G145R mutation on the structure and immunogenic activity of the hepatitis B surface antigen: a computational analysis. Hepat Mon 2016; 16:e39097.
17. Lin Y, Liu C, Chien W, et al. New insights into the evolutionary rate of hepatitis B virus at different biological scales. J Virol 2015; 89:3512–3522.
18. Yang G, Liu Z, Yang J, et al. Quasispecies characteristics in mother-to-child transmission of hepatitis B virus by next-generation sequencing. J Infect 2017; 75:48–58.
19. Du Y, Chi X, Wang C, et al. Quantifying perinatal transmission of hepatitis B viral quasispecies by tag linkage deep sequencing. Sci Rep 2017; 7:10168.
20. Public Health Agency of Canada. Canadian Immunization Guide: Part 4 - Active Vaccines (Hepatitis B Vaccine). Available at: Accessed October 2017.

next-generation sequencing; quasispecies; vaccine escape

Supplemental Digital Content

Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition