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Randomized, multicenter trial of a single dose of AS03-adjuvanted or unadjuvanted H1N1 2009 pandemic influenza vaccine in children 6 months to <9 years of age: safety and immunogenicity.
Langley, Joanne M; Reich, Dennis; Aggarwal, Naresh; Connor, David; Lebel, Marc H; Gupta, Anil; Garfield, Hartley; Li, Ping; Madan, Anu; Vaughn, David W.
Afiliação
  • Langley JM; Canadian Center for Vaccinology and the Departments of Pediatrics and Community Health and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada. jmlangle@dal.ca
Pediatr Infect Dis J ; 31(8): 848-58, 2012 Aug.
Article em En | MEDLINE | ID: mdl-22801094
ABSTRACT

BACKGROUND:

During the 2009-2010 influenza pandemic, we evaluated the immunogenicity and safety of different H1N1 2009 pandemic influenza vaccines delivering various viral hemagglutinin (HA) doses with or without AS03 (a tocopherol oil-in-water emulsion-based adjuvant system) in children (NCT00976820).

METHODS:

Three hundred twenty-two healthy children 6 months to <9 years of age were randomized to receive 2 doses of nonadjuvanted (15 µg or 7.5 µg HA) or adjuvanted vaccine (3.75 µg HA/AS03A or 1.9 µg HA/AS03B), 21 days apart. Blood samples before and after each dose were tested for immune responses using hemagglutination inhibition and microneutralization assays. Safety assessments were done up to day 385.

RESULTS:

The first dose of both AS03-adjuvanted vaccines elicited strong immune responses (seroprotection rates 98.3%/99.0%; seroconversion rates 94.9%/97.0%; geometric mean fold rises 36.2/33.6), which were higher post-dose 2 (seroprotection rate 100.0%/100%; seroconversion rate 100.0%/98.8%; geometric mean fold rise 157.1/151.6), meeting European regulatory criteria on days 21 and 42. The nonadjuvanted 15 µg HA vaccine also met the regulatory criteria after each dose; the 7.5 µg HA vaccine met them only post-dose 2. Six months post-dose 1, all vaccines except the nonadjuvanted 7.5 µg HA vaccine met European regulatory criteria. Neutralizing antibody response paralleled the hemagglutination inhibition immune response after each dose. Pain at the injection site, lasting 2-3 days, was more common following adjuvanted than nonadjuvanted vaccination.

CONCLUSIONS:

AS03-adjuvanted H1N1 2009 pandemic influenza vaccine (3.75 µg or 1.9 µg HA), administered as 2 doses, was highly immunogenic, induced long-term immune response to 6 months, with a clinically acceptable safety profile in children aged 6 months to <9 years of age.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polissorbatos / Esqualeno / Vacinas contra Influenza / Adjuvantes Imunológicos / Tocoferóis / Alfa-Tocoferol / Influenza Humana / Vírus da Influenza A Subtipo H1N1 / Pandemias Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polissorbatos / Esqualeno / Vacinas contra Influenza / Adjuvantes Imunológicos / Tocoferóis / Alfa-Tocoferol / Influenza Humana / Vírus da Influenza A Subtipo H1N1 / Pandemias Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2012 Tipo de documento: Article