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Long-Term Persistence of Antibody Response with Two Doses of Inactivated Hepatitis A Vaccine in Children

INTRODUCTION: Hepatitis A virus infection is more severe in adults than children. Although vaccination can protect adults, current childhood programs cover a large population more successfully. Childhood vaccination is, therefore, a solution to protecting adults if it induces lasting immunity. Fifte...

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Autores principales: Agrawal, Ashish, Kolhapure, Shafi, Andani, Anar, Ota, Martin O. C., Badur, Selim, Karkada, Naveen, Mitra, Monjori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680478/
https://www.ncbi.nlm.nih.gov/pubmed/32710245
http://dx.doi.org/10.1007/s40121-020-00311-8
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author Agrawal, Ashish
Kolhapure, Shafi
Andani, Anar
Ota, Martin O. C.
Badur, Selim
Karkada, Naveen
Mitra, Monjori
author_facet Agrawal, Ashish
Kolhapure, Shafi
Andani, Anar
Ota, Martin O. C.
Badur, Selim
Karkada, Naveen
Mitra, Monjori
author_sort Agrawal, Ashish
collection PubMed
description INTRODUCTION: Hepatitis A virus infection is more severe in adults than children. Although vaccination can protect adults, current childhood programs cover a large population more successfully. Childhood vaccination is, therefore, a solution to protecting adults if it induces lasting immunity. Fifteen-year protection has been demonstrated in children, but longer-term data are only available for adults. We aimed to predict long term persistence of antibody in children beyond 15 years and assess if immunological mechanisms triggered by vaccination support longer-term protection. METHODS: Long-term clinical studies using hepatitis A (HAV) or A/B vaccines (HAB) containing 720 or 1440 Enzyme-linked immunosorbent assay Units (EU) of hepatitis A virus antigen were identified. Duration of persistence of antibodies and possible protection was determined by descriptively comparing antibody geometric mean concentration (GMC) kinetics, as well as GMC (95% confidence interval) at 15 years post-vaccination across studies. Immunological mechanism studies describing hepatitis A vaccination were identified. RESULTS: One study in children 12–15 years (2-dose HAB 720) and four in adults (2-dose HAV 1440 and 3-dose HAB 720) showed comparable GMC kinetics and per year rates of change up to 15 years. At 15 years, the GMC in children [414.7 mEU/ml (336.9; 510.5)] was in the same range as in adults [range 282.6 (217.6; 367.0) to 550.1 (416.0; 727.4)]. Based on these data, mathematical model predictions from adult studies (showing > 85% protected at 50 years) were deemed likely to also apply to children. Studies identified, both humoral and cell-mediated responses are induced following vaccination. CONCLUSION: Based on comparable antibody data in adults and children up to 15 years, similar longer-term antibody persistence is expected in children with 2-dose inactivated hepatitis A 720 containing vaccine at least up to 50 years. Accordingly, improving routine childhood hepatitis A vaccination coverage could protect against more severe disease in adulthood. TRIAL REGISTRATION: ClinicalTrials.gov identifiers, NCT00875485, NCT01000324, NCT01037114, NCT00289757, NCT00291876. SUPPLEMENTARY INFORMATION: The online version supplementary material available at 10.1007/s40121-020-00311-8.
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spelling pubmed-76804782020-11-23 Long-Term Persistence of Antibody Response with Two Doses of Inactivated Hepatitis A Vaccine in Children Agrawal, Ashish Kolhapure, Shafi Andani, Anar Ota, Martin O. C. Badur, Selim Karkada, Naveen Mitra, Monjori Infect Dis Ther Original Research INTRODUCTION: Hepatitis A virus infection is more severe in adults than children. Although vaccination can protect adults, current childhood programs cover a large population more successfully. Childhood vaccination is, therefore, a solution to protecting adults if it induces lasting immunity. Fifteen-year protection has been demonstrated in children, but longer-term data are only available for adults. We aimed to predict long term persistence of antibody in children beyond 15 years and assess if immunological mechanisms triggered by vaccination support longer-term protection. METHODS: Long-term clinical studies using hepatitis A (HAV) or A/B vaccines (HAB) containing 720 or 1440 Enzyme-linked immunosorbent assay Units (EU) of hepatitis A virus antigen were identified. Duration of persistence of antibodies and possible protection was determined by descriptively comparing antibody geometric mean concentration (GMC) kinetics, as well as GMC (95% confidence interval) at 15 years post-vaccination across studies. Immunological mechanism studies describing hepatitis A vaccination were identified. RESULTS: One study in children 12–15 years (2-dose HAB 720) and four in adults (2-dose HAV 1440 and 3-dose HAB 720) showed comparable GMC kinetics and per year rates of change up to 15 years. At 15 years, the GMC in children [414.7 mEU/ml (336.9; 510.5)] was in the same range as in adults [range 282.6 (217.6; 367.0) to 550.1 (416.0; 727.4)]. Based on these data, mathematical model predictions from adult studies (showing > 85% protected at 50 years) were deemed likely to also apply to children. Studies identified, both humoral and cell-mediated responses are induced following vaccination. CONCLUSION: Based on comparable antibody data in adults and children up to 15 years, similar longer-term antibody persistence is expected in children with 2-dose inactivated hepatitis A 720 containing vaccine at least up to 50 years. Accordingly, improving routine childhood hepatitis A vaccination coverage could protect against more severe disease in adulthood. TRIAL REGISTRATION: ClinicalTrials.gov identifiers, NCT00875485, NCT01000324, NCT01037114, NCT00289757, NCT00291876. SUPPLEMENTARY INFORMATION: The online version supplementary material available at 10.1007/s40121-020-00311-8. Springer Healthcare 2020-07-24 2020-12 /pmc/articles/PMC7680478/ /pubmed/32710245 http://dx.doi.org/10.1007/s40121-020-00311-8 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Agrawal, Ashish
Kolhapure, Shafi
Andani, Anar
Ota, Martin O. C.
Badur, Selim
Karkada, Naveen
Mitra, Monjori
Long-Term Persistence of Antibody Response with Two Doses of Inactivated Hepatitis A Vaccine in Children
title Long-Term Persistence of Antibody Response with Two Doses of Inactivated Hepatitis A Vaccine in Children
title_full Long-Term Persistence of Antibody Response with Two Doses of Inactivated Hepatitis A Vaccine in Children
title_fullStr Long-Term Persistence of Antibody Response with Two Doses of Inactivated Hepatitis A Vaccine in Children
title_full_unstemmed Long-Term Persistence of Antibody Response with Two Doses of Inactivated Hepatitis A Vaccine in Children
title_short Long-Term Persistence of Antibody Response with Two Doses of Inactivated Hepatitis A Vaccine in Children
title_sort long-term persistence of antibody response with two doses of inactivated hepatitis a vaccine in children
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680478/
https://www.ncbi.nlm.nih.gov/pubmed/32710245
http://dx.doi.org/10.1007/s40121-020-00311-8
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