Abstract:It is still controversial whether maternal anti-HBV antibodies (anti-HBVs) affect the infants' immune response to hepatitis B virus (HBV) vaccination. This multicentre study aims to address this question. First, we determined whether the transplacental transfer of maternal anti-HBVs occurs by measuring the titres of 90 anti-HBVs-positive pregnant women and their newborns. The anti-HBVs-positive rates of newborns ranged from 89.7% to 100.0%, depending on the maternal anti-HBVs titres. Secondly, we investigated … Show more
“…There have been suggestions that HBV antigens/antibodies can influence the immune response of infants to hepatitis B vaccine . In our study there were no significant differences in anti‐HBs levels between HBV‐exposed and unexposed infants although at 24 months there was a trend towards a lower level in the HBV‐exposed suggesting that further data are needed to determine if different strategies are needed for these infants.…”
Section: Discussioncontrasting
confidence: 58%
“…This is particularly important for infants born to HIV‐positive mothers in whom a decreased response could be observed and in whom HBV transmission may more frequently occur due to high HBV‐DNA levels in co‐infected mothers . Maternal HBV co‐infection could also be potentially associated with a lower response to HBV vaccine since maternal specific antibody can interfere with the infant's own response to vaccination …”
Section: Introductionmentioning
confidence: 99%
“…6,7 Maternal HBV co-infection could also be potentially associated with a lower response to HBV vaccine since maternal specific antibody can interfere with the infant's own response to vaccination. 8 We conducted this study in a cohort of HIV-exposed children in Malawi, a country with an HBV seroprevalence of about 8%, 9 where the HBV vaccine has been introduced since more than 10 years with a high vaccine coverage. 10 This study had the following objectives: (i) To determine the proportion of children with protective anti-HBs response at 6, 12, and 24 months of age; (ii) To identify possible factors associated with a low vaccine response; (iii) To correlate the specific antibody response to HBV infection acquisition.…”
The aim of this study was to assess the immune response to HBV vaccine in HIV-exposed infants and to correlate it to HBV infection acquisition. Protective anti-HBs levels (>10 mIU/mL) were found in 54/58 (93.2%) infants at 6 months, 126/144 (87.5%) at 12 months and 141/176 (80.1%) children at 24 months. HBV infection (seven children were HBsAg + at Month 24) occurred also in the presence of levels above 10 mIU/mL. Our findings indicate limited impact of HIV exposure on anti-HBV immune response, but suggest that levels >10 mIU/mL may be required to confer protection in this context.
“…There have been suggestions that HBV antigens/antibodies can influence the immune response of infants to hepatitis B vaccine . In our study there were no significant differences in anti‐HBs levels between HBV‐exposed and unexposed infants although at 24 months there was a trend towards a lower level in the HBV‐exposed suggesting that further data are needed to determine if different strategies are needed for these infants.…”
Section: Discussioncontrasting
confidence: 58%
“…This is particularly important for infants born to HIV‐positive mothers in whom a decreased response could be observed and in whom HBV transmission may more frequently occur due to high HBV‐DNA levels in co‐infected mothers . Maternal HBV co‐infection could also be potentially associated with a lower response to HBV vaccine since maternal specific antibody can interfere with the infant's own response to vaccination …”
Section: Introductionmentioning
confidence: 99%
“…6,7 Maternal HBV co-infection could also be potentially associated with a lower response to HBV vaccine since maternal specific antibody can interfere with the infant's own response to vaccination. 8 We conducted this study in a cohort of HIV-exposed children in Malawi, a country with an HBV seroprevalence of about 8%, 9 where the HBV vaccine has been introduced since more than 10 years with a high vaccine coverage. 10 This study had the following objectives: (i) To determine the proportion of children with protective anti-HBs response at 6, 12, and 24 months of age; (ii) To identify possible factors associated with a low vaccine response; (iii) To correlate the specific antibody response to HBV infection acquisition.…”
The aim of this study was to assess the immune response to HBV vaccine in HIV-exposed infants and to correlate it to HBV infection acquisition. Protective anti-HBs levels (>10 mIU/mL) were found in 54/58 (93.2%) infants at 6 months, 126/144 (87.5%) at 12 months and 141/176 (80.1%) children at 24 months. HBV infection (seven children were HBsAg + at Month 24) occurred also in the presence of levels above 10 mIU/mL. Our findings indicate limited impact of HIV exposure on anti-HBV immune response, but suggest that levels >10 mIU/mL may be required to confer protection in this context.
“…For live measles vaccine, vaccination in the context of passive immunity is known to dampen the specific humoral response to vaccination [31]. Such attenuating effect of maternally-derived antibodies on human infant humoral vaccine responses has also been observed for the non-live viral vaccines inactivated polio vaccine [32] and hepatitis B vaccine [33], and this is corroborated by a series of animal experimental studies [31], including studies in pigs of non-live Haemophilus parasuis immunization [34]. In humans and pigs alike, the development of active cellmediated immunity may not be compromised by the presence of maternal immunity despite blunted humoral responses, as observed for Mycobacterium hyopneumoniae vaccination of piglets from immunized dams [35] or live measles vaccine in humans [31].…”
“…A large multicenter study by Chen et al of 1,063 mothers who were HBsAg−/anti‐HBs+ and their infants showed a strong negative correlation between maternal anti‐HBs and infant anti‐HBs titers in vaccinated infants. Further, up to 23% of infants born to mothers with protective anti‐HBs titers >10 IU/L did not respond to the standard vaccination series.…”
The hepatitis B virus (HBV) is an important human pathogen. Unvaccinated infants infected through mother-to-child transmission (MTCT) are at >95% risk of developing serum hepatitis B surface antigen-positive chronic hepatitis B (CHB). Despite complete passive-active HBV immunoprophylaxis, approximately 10% of infants born to mothers who are highly viremic develop CHB, and thus maternal treatment with nucleos(t)ide analogs (tenofovir disoproxil fumarate, lamivudine, or telbivudine) is recommended in the third trimester of pregnancy to reduce MTCT risk. Viral rebound usually occurs after stopping treatment and, in the context of maternal immunologic reconstitution postpartum, can also precipitate host immune-mediated hepatic (biochemical) flares. In this article, we review the epidemiology of HBV MTCT, discuss management and potential mechanisms of HBV vertical transmission, and highlight recent studies on virologic and immunologic aspects of hepatitis B in pregnancy and postpartum. (Hepatology Communications 2020;4:157-171).The global prevalence of CHB (serum HBsAg+) is 3.6%, with the highest prevalence in Africa (8.8%) and the Western Pacific (5.2%). More than 75% of individuals with CHB worldwide are found in the Asia Pacific
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