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Hepatitis A antibody persistence 8 and 10 years after 1-dose and 2-dose vaccination in children from Panama.
Juliao, Patricia; Abadia, Ivonne; Welby, Sarah; Wéry, Stéphanie; Wong, Digna; De Léon, Tirza; DeAntonio, Rodrigo; Naranjo, Laura; Guignard, Adrienne; Marano, Cinzia.
Afiliação
  • Juliao P; GSK, Panama. Electronic address: patricia.d.juliao@gsk.com.
  • Abadia I; Instituto de Investigaciones Científicas y Servicios de Alta Tecnología de Panama, Panama City, Panama. Electronic address: josivo@usa.net.
  • Welby S; GSK, Belgium. Electronic address: sarah.x.welby@gsk.com.
  • Wéry S; GSK, Belgium. Electronic address: stephanie.x.wery@gsk.com.
  • Wong D; Instituto de Investigaciones Científicas y Servicios de Alta Tecnología de Panama, Panama City, Panama. Electronic address: dwong@indicasat.org.pa.
  • De Léon T; Unidad Materno-Infantil José Domingo de Obaldia, Chiriqui, Panama. Electronic address: tirzarelis@cwpanama.net.
  • DeAntonio R; Cevaxin, Panama City, Panama. Electronic address: rodrigo.deantonio@cevaxin.com.
  • Naranjo L; GSK, Panama. Electronic address: laura.t.naranjo@gsk.com.
  • Guignard A; GSK, Belgium. Electronic address: adrienne.x.guignard@gsk.com.
  • Marano C; GSK, Italy. Electronic address: cinzia.x.marano@gsk.com.
Vaccine ; 39(1): 26-34, 2021 01 03.
Article em En | MEDLINE | ID: mdl-33239226
BACKGROUND: Hepatitis A virus (HAV) remains a global public health concern, which is potentially growing in Latin America, due to an expected shift from high to intermediate endemicity levels. The use of HAV vaccines in pediatric national immunization programs (NIPs), either as a 2-dose or a 1-dose schedule, has been explored in Latin American countries; however, evidence demonstrating long-term protection in this population is limited in the region. We evaluated long-term antibody persistence following a 1-dose partial series and the recommended 2-dose schedule used in Panama's pediatric NIP. METHODS: Two independent cross-sectional serological surveys were conducted at year 8 (Y8) and Y10 following vaccination under the NIP with 1 or 2 doses of an inactivated HAV vaccine (Havrix, GSK). Seropositivity (anti-HAV antibody concentration ≥ 15 mIU/mL) rates and antibody geometric mean concentrations (GMCs) were assessed at each serosurvey. Non-inferiority of 1 dose versus 2 doses was also explored. RESULTS: This study (NCT02712359) included 600 and 599 children at Y8 and Y10 post-vaccination, respectively. Seropositivity rates were 74.3% (95% confidence interval [CI]: 69.0; 79.2) and 97.7% (95% CI: 95.3; 99.1) at Y8 and 71.9% (95% CI: 66.4; 76.9) and 96.3% (95% CI: 93.5; 98.2) at Y10, in the 1-dose and 2-dose groups, respectively. Antibody GMCs were lower in the 1-dose versus the 2-dose group in both surveys. Non-inferiority was not demonstrated since the lower limit of the 2-sided 95% CI for the between-group difference in seropositivity rates (1-dose minus 2-dose) was < -10%. CONCLUSION: Anti-HAV antibody persistence was observed in lower percentages of children receiving 1 dose versus 2 doses of Havrix, at 8 and 10 years post-vaccination in Panama. Further investigations are needed to confirm antibody persistence and conclude on the protection afforded beyond 10 years in the pediatric population in Latin America.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite A Tipo de estudo: Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Child / Humans País como assunto: America central / Panama Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite A Tipo de estudo: Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Child / Humans País como assunto: America central / Panama Idioma: En Ano de publicação: 2021 Tipo de documento: Article