Izurieta Patricia, Uy-Aragon Mercy Jeane, Dramé Mamadou, Vaughn David W
From the *GSK Vaccines, Wavre, Belgium; †Research Institute for Tropical Medicine, Muntinlupa City, Philippines; and ‡GSK Vaccines, King of Prussia, Pennsylvania.
Pediatr Infect Dis J. 2016 Feb;35(2):e35-47. doi: 10.1097/INF.0000000000000968.
Heterologous prime-boost vaccination is a pandemic response strategy utilizing subtype-matched vaccine at pandemic onset followed by strain-matched vaccine once available. Persistence of immune response and safety of influenza A (H5N1) vaccine adjuvanted with adjuvant system containing α-tocopherol and squalene in an oil-in-water emulsion (AS03B) were evaluated.
An open phase 3 active-controlled study (www.clinicaltrials.gov NCT01379937) assessed immunogenicity and reactogenicity of a heterologous booster dose of A/turkey/Turkey/1/2005-H5N1-AS03B in children 3 to <18 years of age, given 6 months after 2-dose priming with A/Indonesia/05/2005-H5N1-AS03B (H5N1(2) -H5N1 group) compared with a single dose of A/turkey/Turkey/1/2005-H5N1-AS03B in unprimed subjects (hepatitis A vaccine (HAV)-H5N1 group). Hemagglutinin inhibition responses and microneutralization antibodies were assessed to 6 months after booster vaccination.
Hemagglutinin inhibition antibody responses against A/turkey/Turkey/1/2005-H5N1 were superior in the H5N1(2)-H5N1 versus the hepatitis A vaccine-H5N1 group overall and in each age strata (3 to <10 and 10 to <18 years). Anamnestic immune responses were demonstrated against vaccine-homologous/heterologous strains in the H5N1(2)-H5N1 group. Injection site pain and fever increased with consecutive doses for children <6 years (H5N1(2)-H5N1). Immune responses to vaccine-homologous/heterologous strains persisted to 6 months after booster vaccination in the H5N1(2)-H5N1 group.
Heterologous H5N1-AS03B-adjuvanted booster vaccination in children/adolescents was immunogenic for vaccine-homologous and heterologous strains following 2-dose priming, with immune persistence for at least 6 months. Prime-boost strategies using H5N1-AS03 could be effectively employed in this age group.
异源初免 - 加强免疫接种是一种大流行应对策略,在大流行开始时使用亚型匹配疫苗,一旦有可用的毒株匹配疫苗则随后使用。评估了在水包油乳剂中含有α - 生育酚和角鲨烯的佐剂系统(AS03B)佐剂的甲型流感(H5N1)疫苗的免疫反应持久性和安全性。
一项开放的3期活性对照研究(www.clinicaltrials.gov NCT01379937)评估了3至<18岁儿童中异源加强剂量的A/土耳其/土耳其/1/2005 - H5N1 - AS03B的免疫原性和反应原性,在以A/印度尼西亚/05/2005 - H5N1 - AS03B进行2剂初免6个月后给予(H5N1(2) - H5N1组),并与未初免的受试者中单次剂量的A/土耳其/土耳其/1/2005 - H5N1 - AS03B进行比较(甲型肝炎疫苗(HAV) - H5N1组)。在加强接种后6个月评估血凝素抑制反应和微量中和抗体。
总体上以及在每个年龄层(3至<10岁和10至<18岁)中,H5N1(2) - H5N1组针对A/土耳其/土耳其/1/2005 - H5N1的血凝素抑制抗体反应优于甲型肝炎疫苗 - H5N1组。在H5N1(2) - H5N1组中证明了对疫苗同源/异源毒株的回忆性免疫反应。对于<6岁的儿童(H5N1(2) - H5N1),注射部位疼痛和发热随连续剂量增加。在H5N1(2) - H5N1组中,对疫苗同源/异源毒株的免疫反应在加强接种后持续至6个月。
在儿童/青少年中进行异源H5N1 - AS03B佐剂加强接种,在2剂初免后对疫苗同源和异源毒株具有免疫原性,免疫持久性至少为6个月。使用H5N1 - AS03的初免 - 加强策略可有效地应用于该年龄组。