Model based estimates of long-term persistence of inactivated hepatitis A vaccine-induced antibodies in adults.
Abstract
Background In this paper, we review the results of existing statistical models of the long-term persistence of hepatitis A vaccine-induced antibodies in light of recently available immunogenicity data from 2 clinical trials (up to 17 years of follow-up).Methods Healthy adult volunteers monitored annually for 17 years after the administration of the first vaccine dose in 2 double-blind, randomized clinical trials were included in this analysis. Vaccination in these studies was administered according to a 2-dose vaccination schedule: 0, 12 months in study A and 0, 6 months in study B (NCT00289757/NCT00291876). Antibodies were measured using an in-house ELISA during the first 11 years of follow-up; a commercially available ELISA was then used up to Year 17 of follow-up. Long-term antibody persistence from studies A and B was estimated using statistical models for longitudinal data. Data from studies A and B were modeled separately.Results A total of 173 participants in study A and 108 participants in study B were included in the analysis. A linear mixed model with 2 changepoints allowed all available results to be accounted for. Predictions based on this model indicated that 98% (95%CI: 94-100%) of participants in study A and 97% (95%CI: 94-100%) of participants in study B will remain seropositive 25 years after receiving the first vaccine dose. Other models using part of the data provided consistent results: ≥95% of the participants was projected to remain seropositive for ≥25 years.Conclusion This analysis, using previously used and newly selected model structures, was consistent with former estimates of seropositivity rates ≥95% for at least 25 years.
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Kinetic models of antibody decrease among adults indicate that protective levels persist for >40 years.
“Kinetic models of antibody decrease among adults indicate that protective levels persist for >40 years (1302–1304).”
From Sexually Transmitted Infections Treatment Guidelines, 2021 (2021) · cites this paper as [1304]
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- Authors
- Hens, N., Habteab Ghebretinsae, A., Hardt, K., Van Damme, P., & Van Herck, K.
- Affiliations
- University of Antwerp (BE)
- GlaxoSmithKline (Belgium) (BE)
- ORCID
- Hens, Niel
- Venue
- Vaccine
- Publisher
- Elsevier BV
- Published
- 2014-03
- Volume
- 32
- Issue
- 13
- Pages
- 1507-1513
- ISSN
- 0264-410X (ISSN-L)
- OpenAlex
- W2093800471
- Cited by
- 65
- References
- 24
- Citations by year
- 2025: 5 · 2023: 6 · 2022: 2 · 2021: 5 · 2020: 11 · 2019: 6 · 2018: 5 · 2017: 10 · 2016: 4 · 2015: 9 · 2014: 2
- FWCI
- 4.65
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Vaccine (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- Document Server@UHasselt (UHasselt) (submittedVersion)
- Topics
- Health Sciences › Medicine › Hepatology › Hepatitis Viruses Studies and Epidemiology
- Health Sciences › Medicine › Epidemiology › Hepatitis B Virus Studies
- Health Sciences › Medicine › Infectious Diseases › Viral gastroenteritis research and epidemiology
- Keywords
- inactivated hepatitis A vaccine, antibody persistence, vaccine immunogenicity, linear mixed models, change-point models, two-dose vaccination schedule
- MeSH terms
- Adolescent, Adult, Antibody Formation, Female, Follow-Up Studies, Hepatitis A, Humans, Immunization, Secondary, Longitudinal Studies, Male, Vaccines, Inactivated, Linear Models, Hepatitis A Vaccines, Hepatitis A Antibodies, Young Adult
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