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Comparison of Two Hepatitis B Vaccination Strategies Targeting Vertical Transmission: A 10-Year Japanese Multicenter Prospective Cohort Study

In 1985, a hepatitis B (HB) vaccination strategy against vertical HB virus transmission was introduced in Japan that recommended vaccination of infants at two, three, and five months of age (delayed strategy). This schedule was revised in 2013, recommending to vaccinate at birth and at 1 and 6 month...

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Autores principales: Nishimura, Koji, Yamana, Keiji, Fukushima, Sachiyo, Fujioka, Kazumichi, Miyabayashi, Hiroshi, Murabayashi, Masao, Masunaga, Ken, Okahashi, Aya, Nagano, Nobuhiko, Morioka, Ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830287/
https://www.ncbi.nlm.nih.gov/pubmed/33477275
http://dx.doi.org/10.3390/vaccines9010058
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author Nishimura, Koji
Yamana, Keiji
Fukushima, Sachiyo
Fujioka, Kazumichi
Miyabayashi, Hiroshi
Murabayashi, Masao
Masunaga, Ken
Okahashi, Aya
Nagano, Nobuhiko
Morioka, Ichiro
author_facet Nishimura, Koji
Yamana, Keiji
Fukushima, Sachiyo
Fujioka, Kazumichi
Miyabayashi, Hiroshi
Murabayashi, Masao
Masunaga, Ken
Okahashi, Aya
Nagano, Nobuhiko
Morioka, Ichiro
author_sort Nishimura, Koji
collection PubMed
description In 1985, a hepatitis B (HB) vaccination strategy against vertical HB virus transmission was introduced in Japan that recommended vaccination of infants at two, three, and five months of age (delayed strategy). This schedule was revised in 2013, recommending to vaccinate at birth and at 1 and 6 months of age (non-delayed strategy). We aimed to compare the vertical HB virus transmission rates and immunogenic responses between these two vaccination strategies. This Japanese multicenter prospective cohort study included 222 infants born between 2008 and 2017 to serum hepatitis B surface (HBs) antigen (HBsAg)-positive mothers. During the study period, 136 and 86 infants received delayed and non-delayed strategies, respectively. A positive vertical HB virus transmission was defined as a positive serum HBsAg status. Seropositive immunogenic response was defined as a serum anti-HBs titer of ≥10 mIU/mL. Post-vaccination serum HBsAg positivity rates did not differ significantly between the delayed (0/136 [0.0%, 95% confidence interval, 0.0–2.7%]) and non-delayed (2/86 [2.3%, 95% confidence interval, 0.3–8.1%]) strategy groups. Seropositive immunogenic response rates were 100.0% (136/136) and 97.7% (84/86), respectively. Although this study was under-powered to detect a statistically significant result, no vertical HB virus transmission was observed in the delayed strategy.
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spelling pubmed-78302872021-01-26 Comparison of Two Hepatitis B Vaccination Strategies Targeting Vertical Transmission: A 10-Year Japanese Multicenter Prospective Cohort Study Nishimura, Koji Yamana, Keiji Fukushima, Sachiyo Fujioka, Kazumichi Miyabayashi, Hiroshi Murabayashi, Masao Masunaga, Ken Okahashi, Aya Nagano, Nobuhiko Morioka, Ichiro Vaccines (Basel) Article In 1985, a hepatitis B (HB) vaccination strategy against vertical HB virus transmission was introduced in Japan that recommended vaccination of infants at two, three, and five months of age (delayed strategy). This schedule was revised in 2013, recommending to vaccinate at birth and at 1 and 6 months of age (non-delayed strategy). We aimed to compare the vertical HB virus transmission rates and immunogenic responses between these two vaccination strategies. This Japanese multicenter prospective cohort study included 222 infants born between 2008 and 2017 to serum hepatitis B surface (HBs) antigen (HBsAg)-positive mothers. During the study period, 136 and 86 infants received delayed and non-delayed strategies, respectively. A positive vertical HB virus transmission was defined as a positive serum HBsAg status. Seropositive immunogenic response was defined as a serum anti-HBs titer of ≥10 mIU/mL. Post-vaccination serum HBsAg positivity rates did not differ significantly between the delayed (0/136 [0.0%, 95% confidence interval, 0.0–2.7%]) and non-delayed (2/86 [2.3%, 95% confidence interval, 0.3–8.1%]) strategy groups. Seropositive immunogenic response rates were 100.0% (136/136) and 97.7% (84/86), respectively. Although this study was under-powered to detect a statistically significant result, no vertical HB virus transmission was observed in the delayed strategy. MDPI 2021-01-17 /pmc/articles/PMC7830287/ /pubmed/33477275 http://dx.doi.org/10.3390/vaccines9010058 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nishimura, Koji
Yamana, Keiji
Fukushima, Sachiyo
Fujioka, Kazumichi
Miyabayashi, Hiroshi
Murabayashi, Masao
Masunaga, Ken
Okahashi, Aya
Nagano, Nobuhiko
Morioka, Ichiro
Comparison of Two Hepatitis B Vaccination Strategies Targeting Vertical Transmission: A 10-Year Japanese Multicenter Prospective Cohort Study
title Comparison of Two Hepatitis B Vaccination Strategies Targeting Vertical Transmission: A 10-Year Japanese Multicenter Prospective Cohort Study
title_full Comparison of Two Hepatitis B Vaccination Strategies Targeting Vertical Transmission: A 10-Year Japanese Multicenter Prospective Cohort Study
title_fullStr Comparison of Two Hepatitis B Vaccination Strategies Targeting Vertical Transmission: A 10-Year Japanese Multicenter Prospective Cohort Study
title_full_unstemmed Comparison of Two Hepatitis B Vaccination Strategies Targeting Vertical Transmission: A 10-Year Japanese Multicenter Prospective Cohort Study
title_short Comparison of Two Hepatitis B Vaccination Strategies Targeting Vertical Transmission: A 10-Year Japanese Multicenter Prospective Cohort Study
title_sort comparison of two hepatitis b vaccination strategies targeting vertical transmission: a 10-year japanese multicenter prospective cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830287/
https://www.ncbi.nlm.nih.gov/pubmed/33477275
http://dx.doi.org/10.3390/vaccines9010058
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