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A retrospective pooled analysis assessing the effect of age on the immunogenicity of Havrix™ in healthy adults

Over recent decades, the global incidence of hepatitis A virus infection has been reduced by improvements in sanitation infrastructure and through immunization programs. The immunogenicity and field efficacy of the inactivated hepatitis A vaccine (Havrix™, GSK, Belgium) has been demonstrated in clin...

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Published in:Human vaccines & immunotherapeutics 2015-07, Vol.11 (7), p.1729-1734
Main Authors: Van Der Meeren, Olivier, Crasta, Priya, de Ridder, Marc
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creator Van Der Meeren, Olivier
Crasta, Priya
de Ridder, Marc
description Over recent decades, the global incidence of hepatitis A virus infection has been reduced by improvements in sanitation infrastructure and through immunization programs. The immunogenicity and field efficacy of the inactivated hepatitis A vaccine (Havrix™, GSK, Belgium) has been demonstrated in clinical trials, population-impact studies as well as in several outbreak settings. However, immunological data in older populations are limited, with only few studies assessing the immune response of this vaccine in adults aged ≥40 years. This retrospective pooled analysis of 4 2-dose primary vaccination studies compared the immunogenicity and safety of the inactivated hepatitis A vaccine in adults aged ≥40 years with subjects aged 20-30 years (control group; N = 80 in each group). Fifteen days after the first vaccine dose, 79.7% (95% CI: 68.8-88.2) and 92.3% (95% CI: 84.0-97.1) of subjects were seropositive in the ≥40 years and control groups, respectively; 97.5% (95% CI: 91.2-99.7) and 97.4% (95% CI: 91.0-99.7), respectively, were seropositive one month after the first dose. All subjects in both groups (95% CIs: 95.4-100 and 95.3-100, respectively) were seropositive one month after the second dose. Safety profiles were similar in both groups. In conclusion, the inactivated hepatitis A vaccine induced similar immune responses in adults aged ≥40 and 20-30 years one month after the first and second dose whereas younger subjects may demonstrate a higher seroconversion rate 15 days after the first dose.
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Francis Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Human vaccines &amp; immunotherapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Van Der Meeren, Olivier</au><au>Crasta, Priya</au><au>de Ridder, Marc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A retrospective pooled analysis assessing the effect of age on the immunogenicity of Havrix™ in healthy adults</atitle><jtitle>Human vaccines &amp; immunotherapeutics</jtitle><addtitle>Hum Vaccin Immunother</addtitle><date>2015-07-03</date><risdate>2015</risdate><volume>11</volume><issue>7</issue><spage>1729</spage><epage>1734</epage><pages>1729-1734</pages><issn>2164-5515</issn><eissn>2164-554X</eissn><abstract>Over recent decades, the global incidence of hepatitis A virus infection has been reduced by improvements in sanitation infrastructure and through immunization programs. The immunogenicity and field efficacy of the inactivated hepatitis A vaccine (Havrix™, GSK, Belgium) has been demonstrated in clinical trials, population-impact studies as well as in several outbreak settings. However, immunological data in older populations are limited, with only few studies assessing the immune response of this vaccine in adults aged ≥40 years. This retrospective pooled analysis of 4 2-dose primary vaccination studies compared the immunogenicity and safety of the inactivated hepatitis A vaccine in adults aged ≥40 years with subjects aged 20-30 years (control group; N = 80 in each group). Fifteen days after the first vaccine dose, 79.7% (95% CI: 68.8-88.2) and 92.3% (95% CI: 84.0-97.1) of subjects were seropositive in the ≥40 years and control groups, respectively; 97.5% (95% CI: 91.2-99.7) and 97.4% (95% CI: 91.0-99.7), respectively, were seropositive one month after the first dose. All subjects in both groups (95% CIs: 95.4-100 and 95.3-100, respectively) were seropositive one month after the second dose. Safety profiles were similar in both groups. In conclusion, the inactivated hepatitis A vaccine induced similar immune responses in adults aged ≥40 and 20-30 years one month after the first and second dose whereas younger subjects may demonstrate a higher seroconversion rate 15 days after the first dose.</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>26029816</pmid><doi>10.1080/21645515.2015.1045167</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source PubMed Central
subjects Adult
Aging - immunology
CI, confidence interval
ELISA, enzyme-linked immunosorbent assay
Female
Follow-Up Studies
GMC, geometric mean concentration
HAV outbreak
HAV, hepatitis A virus
Havrix
Hepatitis A Antibodies - analysis
Hepatitis A Vaccines - adverse effects
Hepatitis A Vaccines - immunology
HNIG, human normal immunoglobulin
Humans
Immunization Programs
immunogenicity
inactivated hepatitis A vaccine
Male
Meta-Analysis as Topic
Middle Aged
older adults
rapid response
Retrospective Studies
Short Report
TVC, total vaccinated cohort
UK, United Kingdom
Vaccines, Inactivated
WHO, World Health Organization
Young Adult
title A retrospective pooled analysis assessing the effect of age on the immunogenicity of Havrix™ in healthy adults
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